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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research</title>
<author><name sortKey="Wray, Selina" sort="Wray, Selina" uniqKey="Wray S" first="Selina" last="Wray">Selina Wray</name>
<affiliation><nlm:aff id="aff1"><addr-line>Department of Molecular Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Self, Matthew" sort="Self, Matthew" uniqKey="Self M" first="Matthew" last="Self">Matthew Self</name>
<affiliation><nlm:aff id="aff2"><addr-line>Coriell Institute for Medical Research, Camden, New Jersey, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Lewis, Patrick A" sort="Lewis, Patrick A" uniqKey="Lewis P" first="Patrick A." last="Lewis">Patrick A. Lewis</name>
<affiliation><nlm:aff id="aff1"><addr-line>Department of Molecular Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Taanman, Jan Willem" sort="Taanman, Jan Willem" uniqKey="Taanman J" first="Jan-Willem" last="Taanman">Jan-Willem Taanman</name>
<affiliation><nlm:aff id="aff4"><addr-line>Department of Clinical Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Ryan, Natalie S" sort="Ryan, Natalie S" uniqKey="Ryan N" first="Natalie S." last="Ryan">Natalie S. Ryan</name>
<affiliation><nlm:aff id="aff3"><addr-line>Dementia Research Centre, Department of Neurodegenerative Diseases, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Mahoney, Colin J" sort="Mahoney, Colin J" uniqKey="Mahoney C" first="Colin J." last="Mahoney">Colin J. Mahoney</name>
<affiliation><nlm:aff id="aff3"><addr-line>Dementia Research Centre, Department of Neurodegenerative Diseases, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Liang, Yuying" sort="Liang, Yuying" uniqKey="Liang Y" first="Yuying" last="Liang">Yuying Liang</name>
<affiliation><nlm:aff id="aff3"><addr-line>Dementia Research Centre, Department of Neurodegenerative Diseases, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Devine, Michael J" sort="Devine, Michael J" uniqKey="Devine M" first="Michael J." last="Devine">Michael J. Devine</name>
<affiliation><nlm:aff id="aff1"><addr-line>Department of Molecular Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Sheerin, Una Marie" sort="Sheerin, Una Marie" uniqKey="Sheerin U" first="Una-Marie" last="Sheerin">Una-Marie Sheerin</name>
<affiliation><nlm:aff id="aff1"><addr-line>Department of Molecular Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Houlden, Henry" sort="Houlden, Henry" uniqKey="Houlden H" first="Henry" last="Houlden">Henry Houlden</name>
<affiliation><nlm:aff id="aff1"><addr-line>Department of Molecular Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Morris, Huw R" sort="Morris, Huw R" uniqKey="Morris H" first="Huw R." last="Morris">Huw R. Morris</name>
<affiliation><nlm:aff id="aff5"><addr-line>Cardiff University School of Medicine, University of Cardiff, Cardiff, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Healy, Daniel" sort="Healy, Daniel" uniqKey="Healy D" first="Daniel" last="Healy">Daniel Healy</name>
<affiliation><nlm:aff id="aff4"><addr-line>Department of Clinical Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Marti Masso, Jose Felix" sort="Marti Masso, Jose Felix" uniqKey="Marti Masso J" first="Jose-Felix" last="Marti-Masso">Jose-Felix Marti-Masso</name>
<affiliation><nlm:aff id="aff6"><addr-line>Hospital Donastia, San Sebastian, Spain</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Preza, Elisavet" sort="Preza, Elisavet" uniqKey="Preza E" first="Elisavet" last="Preza">Elisavet Preza</name>
<affiliation><nlm:aff id="aff1"><addr-line>Department of Molecular Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Barker, Suzanne" sort="Barker, Suzanne" uniqKey="Barker S" first="Suzanne" last="Barker">Suzanne Barker</name>
<affiliation><nlm:aff id="aff3"><addr-line>Dementia Research Centre, Department of Neurodegenerative Diseases, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Sutherland, Margaret" sort="Sutherland, Margaret" uniqKey="Sutherland M" first="Margaret" last="Sutherland">Margaret Sutherland</name>
<affiliation><nlm:aff id="aff7"><addr-line>National Institute for Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Corriveau, Roderick A" sort="Corriveau, Roderick A" uniqKey="Corriveau R" first="Roderick A." last="Corriveau">Roderick A. Corriveau</name>
<affiliation><nlm:aff id="aff7"><addr-line>National Institute for Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="D Andrea, Michael" sort="D Andrea, Michael" uniqKey="D Andrea M" first="Michael" last="D'Andrea">Michael D'Andrea</name>
<affiliation><nlm:aff id="aff2"><addr-line>Coriell Institute for Medical Research, Camden, New Jersey, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Schapira, Anthony H V" sort="Schapira, Anthony H V" uniqKey="Schapira A" first="Anthony H. V." last="Schapira">Anthony H. V. Schapira</name>
<affiliation><nlm:aff id="aff4"><addr-line>Department of Clinical Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Uitti, Ryan J" sort="Uitti, Ryan J" uniqKey="Uitti R" first="Ryan J." last="Uitti">Ryan J. Uitti</name>
<affiliation><nlm:aff id="aff8"><addr-line>Departments of Neurology and Neuroscience, Mayo Clinic Jacksonville, Jacksonville, Florida, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Guttman, Mark" sort="Guttman, Mark" uniqKey="Guttman M" first="Mark" last="Guttman">Mark Guttman</name>
<affiliation><nlm:aff id="aff9"><addr-line>Department of Neurology, Center for Movement Disorders, Ontario, Canada</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Opala, Grzegorz" sort="Opala, Grzegorz" uniqKey="Opala G" first="Grzegorz" last="Opala">Grzegorz Opala</name>
<affiliation><nlm:aff id="aff10"><addr-line>Department of Neurology, Medical University of Silesia, Katowice, Poland</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Jasinska Myga, Barbara" sort="Jasinska Myga, Barbara" uniqKey="Jasinska Myga B" first="Barbara" last="Jasinska-Myga">Barbara Jasinska-Myga</name>
<affiliation><nlm:aff id="aff10"><addr-line>Department of Neurology, Medical University of Silesia, Katowice, Poland</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Puschmann, Andreas" sort="Puschmann, Andreas" uniqKey="Puschmann A" first="Andreas" last="Puschmann">Andreas Puschmann</name>
<affiliation><nlm:aff id="aff11"><addr-line>Department of Geriatric Psychiatry, Lund University, Lund, Sweden</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Nilsson, Christer" sort="Nilsson, Christer" uniqKey="Nilsson C" first="Christer" last="Nilsson">Christer Nilsson</name>
<affiliation><nlm:aff id="aff11"><addr-line>Department of Geriatric Psychiatry, Lund University, Lund, Sweden</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Espay, Alberto J" sort="Espay, Alberto J" uniqKey="Espay A" first="Alberto J." last="Espay">Alberto J. Espay</name>
<affiliation><nlm:aff id="aff12"><addr-line>Department of Neurology, University of Cincinnati, Cincinnati, Ohio, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Slawek, Jaroslaw" sort="Slawek, Jaroslaw" uniqKey="Slawek J" first="Jaroslaw" last="Slawek">Jaroslaw Slawek</name>
<affiliation><nlm:aff id="aff13"><addr-line>Department of Neurological and Psychiatric Nursing, Medical University of Gdansk, Gdansk, Poland</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Gutmann, Ludwig" sort="Gutmann, Ludwig" uniqKey="Gutmann L" first="Ludwig" last="Gutmann">Ludwig Gutmann</name>
<affiliation><nlm:aff id="aff14"><addr-line>Department of Neurology , West Virginia University, West Virginia, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Boeve, Bradley F" sort="Boeve, Bradley F" uniqKey="Boeve B" first="Bradley F." last="Boeve">Bradley F. Boeve</name>
<affiliation><nlm:aff id="aff15"><addr-line>Department of Neurology, Mayo Clinic, Rochester, Minnesota, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Boylan, Kevin" sort="Boylan, Kevin" uniqKey="Boylan K" first="Kevin" last="Boylan">Kevin Boylan</name>
<affiliation><nlm:aff id="aff8"><addr-line>Departments of Neurology and Neuroscience, Mayo Clinic Jacksonville, Jacksonville, Florida, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Stoessl, A Jon" sort="Stoessl, A Jon" uniqKey="Stoessl A" first="A. Jon" last="Stoessl">A. Jon Stoessl</name>
<affiliation><nlm:aff id="aff16"><addr-line>Division of Neurology, Pacific Parkinson's Research Centre, University of British Columbia, Vancouver, British Columbia, Canada</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Ross, Owen A" sort="Ross, Owen A" uniqKey="Ross O" first="Owen A." last="Ross">Owen A. Ross</name>
<affiliation><nlm:aff id="aff8"><addr-line>Departments of Neurology and Neuroscience, Mayo Clinic Jacksonville, Jacksonville, Florida, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Maragakis, Nicholas J" sort="Maragakis, Nicholas J" uniqKey="Maragakis N" first="Nicholas J." last="Maragakis">Nicholas J. Maragakis</name>
<affiliation><nlm:aff id="aff17"><addr-line>Department of Neurology and Neuroscience, School of Medicine, Johns Hopkins University, Baltimore, Maryland, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Van Gerpen, Jay" sort="Van Gerpen, Jay" uniqKey="Van Gerpen J" first="Jay" last="Van Gerpen">Jay Van Gerpen</name>
<affiliation><nlm:aff id="aff8"><addr-line>Departments of Neurology and Neuroscience, Mayo Clinic Jacksonville, Jacksonville, Florida, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Gerstenhaber, Melissa" sort="Gerstenhaber, Melissa" uniqKey="Gerstenhaber M" first="Melissa" last="Gerstenhaber">Melissa Gerstenhaber</name>
<affiliation><nlm:aff id="aff18"><addr-line>Department of Psychiatry and Behavioural Sciences, John Hopkins University School of Medicine, Baltimore, Maryland, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Gwinn, Katrina" sort="Gwinn, Katrina" uniqKey="Gwinn K" first="Katrina" last="Gwinn">Katrina Gwinn</name>
<affiliation><nlm:aff id="aff23"><addr-line>Baylor College of Medicine, Department of Genetics, Houston, Texas, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Dawson, Ted M" sort="Dawson, Ted M" uniqKey="Dawson T" first="Ted M." last="Dawson">Ted M. Dawson</name>
<affiliation><nlm:aff id="aff19"><addr-line>Neuroregeneration Program, Institute of Cell Engineering, Department of Neurology and the Solomon H. Snyder Department of Neuroscience, John Hopkins University, Baltimore, Maryland, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Isacson, Ole" sort="Isacson, Ole" uniqKey="Isacson O" first="Ole" last="Isacson">Ole Isacson</name>
<affiliation><nlm:aff id="aff20"><addr-line>Center for Neuroregeneration Research, Harvard Medical School, Belmont, Massachusetts, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Marder, Karen S" sort="Marder, Karen S" uniqKey="Marder K" first="Karen S." last="Marder">Karen S. Marder</name>
<affiliation><nlm:aff id="aff21"><addr-line>Department of Neurology, Psychiatry, Sergievsky Center, and Taub Institute, College of Physicians and Surgeons, Columbia University, New York, New York, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Clark, Lorraine N" sort="Clark, Lorraine N" uniqKey="Clark L" first="Lorraine N." last="Clark">Lorraine N. Clark</name>
<affiliation><nlm:aff id="aff21"><addr-line>Department of Neurology, Psychiatry, Sergievsky Center, and Taub Institute, College of Physicians and Surgeons, Columbia University, New York, New York, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Przedborski, Serge E" sort="Przedborski, Serge E" uniqKey="Przedborski S" first="Serge E." last="Przedborski">Serge E. Przedborski</name>
<affiliation><nlm:aff id="aff22"><addr-line>Center for Motor Neuron Biology and Diseases, Departments of Neurology, Pathology and Cell Biology, College of Physicians and Surgeons, Columbia University, New York, New York, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Finkbeiner, Steven" sort="Finkbeiner, Steven" uniqKey="Finkbeiner S" first="Steven" last="Finkbeiner">Steven Finkbeiner</name>
<affiliation><nlm:aff id="aff24"><addr-line>Gladstone Institute of Neurological Disease, Taube-Koret Center for Huntington's Disease Research, Departments of Neurology and Physiology, University of California San Francisco, San Francisco, California, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Rothstein, Jeffrey D" sort="Rothstein, Jeffrey D" uniqKey="Rothstein J" first="Jeffrey D." last="Rothstein">Jeffrey D. Rothstein</name>
<affiliation><nlm:aff id="aff18"><addr-line>Department of Psychiatry and Behavioural Sciences, John Hopkins University School of Medicine, Baltimore, Maryland, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Wszolek, Zbigniew K" sort="Wszolek, Zbigniew K" uniqKey="Wszolek Z" first="Zbigniew K." last="Wszolek">Zbigniew K. Wszolek</name>
<affiliation><nlm:aff id="aff8"><addr-line>Departments of Neurology and Neuroscience, Mayo Clinic Jacksonville, Jacksonville, Florida, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Rossor, Martin N" sort="Rossor, Martin N" uniqKey="Rossor M" first="Martin N." last="Rossor">Martin N. Rossor</name>
<affiliation><nlm:aff id="aff3"><addr-line>Dementia Research Centre, Department of Neurodegenerative Diseases, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Hardy, John" sort="Hardy, John" uniqKey="Hardy J" first="John" last="Hardy">John Hardy</name>
<affiliation><nlm:aff id="aff1"><addr-line>Department of Molecular Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PMC</idno>
<idno type="pmid">22952635</idno>
<idno type="pmc">3428297</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428297</idno>
<idno type="RBID">PMC:3428297</idno>
<idno type="doi">10.1371/journal.pone.0043099</idno>
<date when="2012">2012</date>
<idno type="wicri:Area/Pmc/Corpus">000A83</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000A83</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research</title>
<author><name sortKey="Wray, Selina" sort="Wray, Selina" uniqKey="Wray S" first="Selina" last="Wray">Selina Wray</name>
<affiliation><nlm:aff id="aff1"><addr-line>Department of Molecular Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Self, Matthew" sort="Self, Matthew" uniqKey="Self M" first="Matthew" last="Self">Matthew Self</name>
<affiliation><nlm:aff id="aff2"><addr-line>Coriell Institute for Medical Research, Camden, New Jersey, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Lewis, Patrick A" sort="Lewis, Patrick A" uniqKey="Lewis P" first="Patrick A." last="Lewis">Patrick A. Lewis</name>
<affiliation><nlm:aff id="aff1"><addr-line>Department of Molecular Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Taanman, Jan Willem" sort="Taanman, Jan Willem" uniqKey="Taanman J" first="Jan-Willem" last="Taanman">Jan-Willem Taanman</name>
<affiliation><nlm:aff id="aff4"><addr-line>Department of Clinical Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Ryan, Natalie S" sort="Ryan, Natalie S" uniqKey="Ryan N" first="Natalie S." last="Ryan">Natalie S. Ryan</name>
<affiliation><nlm:aff id="aff3"><addr-line>Dementia Research Centre, Department of Neurodegenerative Diseases, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Mahoney, Colin J" sort="Mahoney, Colin J" uniqKey="Mahoney C" first="Colin J." last="Mahoney">Colin J. Mahoney</name>
<affiliation><nlm:aff id="aff3"><addr-line>Dementia Research Centre, Department of Neurodegenerative Diseases, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Liang, Yuying" sort="Liang, Yuying" uniqKey="Liang Y" first="Yuying" last="Liang">Yuying Liang</name>
<affiliation><nlm:aff id="aff3"><addr-line>Dementia Research Centre, Department of Neurodegenerative Diseases, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Devine, Michael J" sort="Devine, Michael J" uniqKey="Devine M" first="Michael J." last="Devine">Michael J. Devine</name>
<affiliation><nlm:aff id="aff1"><addr-line>Department of Molecular Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Sheerin, Una Marie" sort="Sheerin, Una Marie" uniqKey="Sheerin U" first="Una-Marie" last="Sheerin">Una-Marie Sheerin</name>
<affiliation><nlm:aff id="aff1"><addr-line>Department of Molecular Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Houlden, Henry" sort="Houlden, Henry" uniqKey="Houlden H" first="Henry" last="Houlden">Henry Houlden</name>
<affiliation><nlm:aff id="aff1"><addr-line>Department of Molecular Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Morris, Huw R" sort="Morris, Huw R" uniqKey="Morris H" first="Huw R." last="Morris">Huw R. Morris</name>
<affiliation><nlm:aff id="aff5"><addr-line>Cardiff University School of Medicine, University of Cardiff, Cardiff, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Healy, Daniel" sort="Healy, Daniel" uniqKey="Healy D" first="Daniel" last="Healy">Daniel Healy</name>
<affiliation><nlm:aff id="aff4"><addr-line>Department of Clinical Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Marti Masso, Jose Felix" sort="Marti Masso, Jose Felix" uniqKey="Marti Masso J" first="Jose-Felix" last="Marti-Masso">Jose-Felix Marti-Masso</name>
<affiliation><nlm:aff id="aff6"><addr-line>Hospital Donastia, San Sebastian, Spain</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Preza, Elisavet" sort="Preza, Elisavet" uniqKey="Preza E" first="Elisavet" last="Preza">Elisavet Preza</name>
<affiliation><nlm:aff id="aff1"><addr-line>Department of Molecular Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Barker, Suzanne" sort="Barker, Suzanne" uniqKey="Barker S" first="Suzanne" last="Barker">Suzanne Barker</name>
<affiliation><nlm:aff id="aff3"><addr-line>Dementia Research Centre, Department of Neurodegenerative Diseases, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Sutherland, Margaret" sort="Sutherland, Margaret" uniqKey="Sutherland M" first="Margaret" last="Sutherland">Margaret Sutherland</name>
<affiliation><nlm:aff id="aff7"><addr-line>National Institute for Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Corriveau, Roderick A" sort="Corriveau, Roderick A" uniqKey="Corriveau R" first="Roderick A." last="Corriveau">Roderick A. Corriveau</name>
<affiliation><nlm:aff id="aff7"><addr-line>National Institute for Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="D Andrea, Michael" sort="D Andrea, Michael" uniqKey="D Andrea M" first="Michael" last="D'Andrea">Michael D'Andrea</name>
<affiliation><nlm:aff id="aff2"><addr-line>Coriell Institute for Medical Research, Camden, New Jersey, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Schapira, Anthony H V" sort="Schapira, Anthony H V" uniqKey="Schapira A" first="Anthony H. V." last="Schapira">Anthony H. V. Schapira</name>
<affiliation><nlm:aff id="aff4"><addr-line>Department of Clinical Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Uitti, Ryan J" sort="Uitti, Ryan J" uniqKey="Uitti R" first="Ryan J." last="Uitti">Ryan J. Uitti</name>
<affiliation><nlm:aff id="aff8"><addr-line>Departments of Neurology and Neuroscience, Mayo Clinic Jacksonville, Jacksonville, Florida, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Guttman, Mark" sort="Guttman, Mark" uniqKey="Guttman M" first="Mark" last="Guttman">Mark Guttman</name>
<affiliation><nlm:aff id="aff9"><addr-line>Department of Neurology, Center for Movement Disorders, Ontario, Canada</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Opala, Grzegorz" sort="Opala, Grzegorz" uniqKey="Opala G" first="Grzegorz" last="Opala">Grzegorz Opala</name>
<affiliation><nlm:aff id="aff10"><addr-line>Department of Neurology, Medical University of Silesia, Katowice, Poland</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Jasinska Myga, Barbara" sort="Jasinska Myga, Barbara" uniqKey="Jasinska Myga B" first="Barbara" last="Jasinska-Myga">Barbara Jasinska-Myga</name>
<affiliation><nlm:aff id="aff10"><addr-line>Department of Neurology, Medical University of Silesia, Katowice, Poland</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Puschmann, Andreas" sort="Puschmann, Andreas" uniqKey="Puschmann A" first="Andreas" last="Puschmann">Andreas Puschmann</name>
<affiliation><nlm:aff id="aff11"><addr-line>Department of Geriatric Psychiatry, Lund University, Lund, Sweden</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Nilsson, Christer" sort="Nilsson, Christer" uniqKey="Nilsson C" first="Christer" last="Nilsson">Christer Nilsson</name>
<affiliation><nlm:aff id="aff11"><addr-line>Department of Geriatric Psychiatry, Lund University, Lund, Sweden</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Espay, Alberto J" sort="Espay, Alberto J" uniqKey="Espay A" first="Alberto J." last="Espay">Alberto J. Espay</name>
<affiliation><nlm:aff id="aff12"><addr-line>Department of Neurology, University of Cincinnati, Cincinnati, Ohio, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Slawek, Jaroslaw" sort="Slawek, Jaroslaw" uniqKey="Slawek J" first="Jaroslaw" last="Slawek">Jaroslaw Slawek</name>
<affiliation><nlm:aff id="aff13"><addr-line>Department of Neurological and Psychiatric Nursing, Medical University of Gdansk, Gdansk, Poland</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Gutmann, Ludwig" sort="Gutmann, Ludwig" uniqKey="Gutmann L" first="Ludwig" last="Gutmann">Ludwig Gutmann</name>
<affiliation><nlm:aff id="aff14"><addr-line>Department of Neurology , West Virginia University, West Virginia, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Boeve, Bradley F" sort="Boeve, Bradley F" uniqKey="Boeve B" first="Bradley F." last="Boeve">Bradley F. Boeve</name>
<affiliation><nlm:aff id="aff15"><addr-line>Department of Neurology, Mayo Clinic, Rochester, Minnesota, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Boylan, Kevin" sort="Boylan, Kevin" uniqKey="Boylan K" first="Kevin" last="Boylan">Kevin Boylan</name>
<affiliation><nlm:aff id="aff8"><addr-line>Departments of Neurology and Neuroscience, Mayo Clinic Jacksonville, Jacksonville, Florida, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Stoessl, A Jon" sort="Stoessl, A Jon" uniqKey="Stoessl A" first="A. Jon" last="Stoessl">A. Jon Stoessl</name>
<affiliation><nlm:aff id="aff16"><addr-line>Division of Neurology, Pacific Parkinson's Research Centre, University of British Columbia, Vancouver, British Columbia, Canada</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Ross, Owen A" sort="Ross, Owen A" uniqKey="Ross O" first="Owen A." last="Ross">Owen A. Ross</name>
<affiliation><nlm:aff id="aff8"><addr-line>Departments of Neurology and Neuroscience, Mayo Clinic Jacksonville, Jacksonville, Florida, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Maragakis, Nicholas J" sort="Maragakis, Nicholas J" uniqKey="Maragakis N" first="Nicholas J." last="Maragakis">Nicholas J. Maragakis</name>
<affiliation><nlm:aff id="aff17"><addr-line>Department of Neurology and Neuroscience, School of Medicine, Johns Hopkins University, Baltimore, Maryland, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Van Gerpen, Jay" sort="Van Gerpen, Jay" uniqKey="Van Gerpen J" first="Jay" last="Van Gerpen">Jay Van Gerpen</name>
<affiliation><nlm:aff id="aff8"><addr-line>Departments of Neurology and Neuroscience, Mayo Clinic Jacksonville, Jacksonville, Florida, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Gerstenhaber, Melissa" sort="Gerstenhaber, Melissa" uniqKey="Gerstenhaber M" first="Melissa" last="Gerstenhaber">Melissa Gerstenhaber</name>
<affiliation><nlm:aff id="aff18"><addr-line>Department of Psychiatry and Behavioural Sciences, John Hopkins University School of Medicine, Baltimore, Maryland, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Gwinn, Katrina" sort="Gwinn, Katrina" uniqKey="Gwinn K" first="Katrina" last="Gwinn">Katrina Gwinn</name>
<affiliation><nlm:aff id="aff23"><addr-line>Baylor College of Medicine, Department of Genetics, Houston, Texas, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Dawson, Ted M" sort="Dawson, Ted M" uniqKey="Dawson T" first="Ted M." last="Dawson">Ted M. Dawson</name>
<affiliation><nlm:aff id="aff19"><addr-line>Neuroregeneration Program, Institute of Cell Engineering, Department of Neurology and the Solomon H. Snyder Department of Neuroscience, John Hopkins University, Baltimore, Maryland, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Isacson, Ole" sort="Isacson, Ole" uniqKey="Isacson O" first="Ole" last="Isacson">Ole Isacson</name>
<affiliation><nlm:aff id="aff20"><addr-line>Center for Neuroregeneration Research, Harvard Medical School, Belmont, Massachusetts, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Marder, Karen S" sort="Marder, Karen S" uniqKey="Marder K" first="Karen S." last="Marder">Karen S. Marder</name>
<affiliation><nlm:aff id="aff21"><addr-line>Department of Neurology, Psychiatry, Sergievsky Center, and Taub Institute, College of Physicians and Surgeons, Columbia University, New York, New York, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Clark, Lorraine N" sort="Clark, Lorraine N" uniqKey="Clark L" first="Lorraine N." last="Clark">Lorraine N. Clark</name>
<affiliation><nlm:aff id="aff21"><addr-line>Department of Neurology, Psychiatry, Sergievsky Center, and Taub Institute, College of Physicians and Surgeons, Columbia University, New York, New York, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Przedborski, Serge E" sort="Przedborski, Serge E" uniqKey="Przedborski S" first="Serge E." last="Przedborski">Serge E. Przedborski</name>
<affiliation><nlm:aff id="aff22"><addr-line>Center for Motor Neuron Biology and Diseases, Departments of Neurology, Pathology and Cell Biology, College of Physicians and Surgeons, Columbia University, New York, New York, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Finkbeiner, Steven" sort="Finkbeiner, Steven" uniqKey="Finkbeiner S" first="Steven" last="Finkbeiner">Steven Finkbeiner</name>
<affiliation><nlm:aff id="aff24"><addr-line>Gladstone Institute of Neurological Disease, Taube-Koret Center for Huntington's Disease Research, Departments of Neurology and Physiology, University of California San Francisco, San Francisco, California, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Rothstein, Jeffrey D" sort="Rothstein, Jeffrey D" uniqKey="Rothstein J" first="Jeffrey D." last="Rothstein">Jeffrey D. Rothstein</name>
<affiliation><nlm:aff id="aff18"><addr-line>Department of Psychiatry and Behavioural Sciences, John Hopkins University School of Medicine, Baltimore, Maryland, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Wszolek, Zbigniew K" sort="Wszolek, Zbigniew K" uniqKey="Wszolek Z" first="Zbigniew K." last="Wszolek">Zbigniew K. Wszolek</name>
<affiliation><nlm:aff id="aff8"><addr-line>Departments of Neurology and Neuroscience, Mayo Clinic Jacksonville, Jacksonville, Florida, United States of America</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Rossor, Martin N" sort="Rossor, Martin N" uniqKey="Rossor M" first="Martin N." last="Rossor">Martin N. Rossor</name>
<affiliation><nlm:aff id="aff3"><addr-line>Dementia Research Centre, Department of Neurodegenerative Diseases, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
<author><name sortKey="Hardy, John" sort="Hardy, John" uniqKey="Hardy J" first="John" last="Hardy">John Hardy</name>
<affiliation><nlm:aff id="aff1"><addr-line>Department of Molecular Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</nlm:aff>
</affiliation>
</author>
</analytic>
<series><title level="j">PLoS ONE</title>
<idno type="eISSN">1932-6203</idno>
<imprint><date when="2012">2012</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass></textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en"><p>Our understanding of the molecular mechanisms of many neurological disorders has been greatly enhanced by the discovery of mutations in genes linked to familial forms of these diseases. These have facilitated the generation of cell and animal models that can be used to understand the underlying molecular pathology. Recently, there has been a surge of interest in the use of patient-derived cells, due to the development of induced pluripotent stem cells and their subsequent differentiation into neurons and glia. Access to patient cell lines carrying the relevant mutations is a limiting factor for many centres wishing to pursue this research. We have therefore generated an open-access collection of fibroblast lines from patients carrying mutations linked to neurological disease. These cell lines have been deposited in the National Institute for Neurological Disorders and Stroke (NINDS) Repository at the Coriell Institute for Medical Research and can be requested by any research group for use in <italic>in vitro</italic>
disease modelling. There are currently 71 mutation-defined cell lines available for request from a wide range of neurological disorders and this collection will be continually expanded. This represents a significant resource that will advance the use of patient cells as disease models by the scientific community.</p>
</div>
</front>
<back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Goate, A" uniqKey="Goate A">A Goate</name>
</author>
<author><name sortKey="Chartier Harlin, Mc" uniqKey="Chartier Harlin M">MC Chartier-Harlin</name>
</author>
<author><name sortKey="Mullan, M" uniqKey="Mullan M">M Mullan</name>
</author>
<author><name sortKey="Brown, J" uniqKey="Brown J">J Brown</name>
</author>
<author><name sortKey="Crawford, F" uniqKey="Crawford F">F Crawford</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Levy Lahad, E" uniqKey="Levy Lahad E">E Levy-Lahad</name>
</author>
<author><name sortKey="Wasco, W" uniqKey="Wasco W">W Wasco</name>
</author>
<author><name sortKey="Poorkaj, P" uniqKey="Poorkaj P">P Poorkaj</name>
</author>
<author><name sortKey="Romano, Dm" uniqKey="Romano D">DM Romano</name>
</author>
<author><name sortKey="Oshima, J" uniqKey="Oshima J">J Oshima</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Rogaev, Ei" uniqKey="Rogaev E">EI Rogaev</name>
</author>
<author><name sortKey="Sherrington, R" uniqKey="Sherrington R">R Sherrington</name>
</author>
<author><name sortKey="Rogaeva, Ea" uniqKey="Rogaeva E">EA Rogaeva</name>
</author>
<author><name sortKey="Levesque, G" uniqKey="Levesque G">G Levesque</name>
</author>
<author><name sortKey="Ikeda, M" uniqKey="Ikeda M">M Ikeda</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Sherrington, R" uniqKey="Sherrington R">R Sherrington</name>
</author>
<author><name sortKey="Rogaev, Ei" uniqKey="Rogaev E">EI Rogaev</name>
</author>
<author><name sortKey="Liang, Y" uniqKey="Liang Y">Y Liang</name>
</author>
<author><name sortKey="Rogaeva, Ea" uniqKey="Rogaeva E">EA Rogaeva</name>
</author>
<author><name sortKey="Levesque, G" uniqKey="Levesque G">G Levesque</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Kitada, T" uniqKey="Kitada T">T Kitada</name>
</author>
<author><name sortKey="Asakawa, S" uniqKey="Asakawa S">S Asakawa</name>
</author>
<author><name sortKey="Hattori, N" uniqKey="Hattori N">N Hattori</name>
</author>
<author><name sortKey="Matsumine, H" uniqKey="Matsumine H">H Matsumine</name>
</author>
<author><name sortKey="Yamamura, Y" uniqKey="Yamamura Y">Y Yamamura</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Paisan Ruiz, C" uniqKey="Paisan Ruiz C">C Paisan-Ruiz</name>
</author>
<author><name sortKey="Jain, S" uniqKey="Jain S">S Jain</name>
</author>
<author><name sortKey="Evans, Ew" uniqKey="Evans E">EW Evans</name>
</author>
<author><name sortKey="Gilks, Wp" uniqKey="Gilks W">WP Gilks</name>
</author>
<author><name sortKey="Simon, J" uniqKey="Simon J">J Simon</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Sidransky, E" uniqKey="Sidransky E">E Sidransky</name>
</author>
<author><name sortKey="Nalls, Ma" uniqKey="Nalls M">MA Nalls</name>
</author>
<author><name sortKey="Aasly, Jo" uniqKey="Aasly J">JO Aasly</name>
</author>
<author><name sortKey="Aharon Peretz, J" uniqKey="Aharon Peretz J">J Aharon-Peretz</name>
</author>
<author><name sortKey="Annesi, G" uniqKey="Annesi G">G Annesi</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Singleton, Ab" uniqKey="Singleton A">AB Singleton</name>
</author>
<author><name sortKey="Farrer, M" uniqKey="Farrer M">M Farrer</name>
</author>
<author><name sortKey="Johnson, J" uniqKey="Johnson J">J Johnson</name>
</author>
<author><name sortKey="Singleton, A" uniqKey="Singleton A">A Singleton</name>
</author>
<author><name sortKey="Hague, S" uniqKey="Hague S">S Hague</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Valente, Em" uniqKey="Valente E">EM Valente</name>
</author>
<author><name sortKey="Abou Sleiman, Pm" uniqKey="Abou Sleiman P">PM Abou-Sleiman</name>
</author>
<author><name sortKey="Caputo, V" uniqKey="Caputo V">V Caputo</name>
</author>
<author><name sortKey="Muqit, Mm" uniqKey="Muqit M">MM Muqit</name>
</author>
<author><name sortKey="Harvey, K" uniqKey="Harvey K">K Harvey</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Rosen, Dr" uniqKey="Rosen D">DR Rosen</name>
</author>
<author><name sortKey="Siddique, T" uniqKey="Siddique T">T Siddique</name>
</author>
<author><name sortKey="Patterson, D" uniqKey="Patterson D">D Patterson</name>
</author>
<author><name sortKey="Figlewicz, Da" uniqKey="Figlewicz D">DA Figlewicz</name>
</author>
<author><name sortKey="Sapp, P" uniqKey="Sapp P">P Sapp</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Sreedharan, J" uniqKey="Sreedharan J">J Sreedharan</name>
</author>
<author><name sortKey="Blair, Ip" uniqKey="Blair I">IP Blair</name>
</author>
<author><name sortKey="Tripathi, Vb" uniqKey="Tripathi V">VB Tripathi</name>
</author>
<author><name sortKey="Hu, X" uniqKey="Hu X">X Hu</name>
</author>
<author><name sortKey="Vance, C" uniqKey="Vance C">C Vance</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Vance, C" uniqKey="Vance C">C Vance</name>
</author>
<author><name sortKey="Rogelj, B" uniqKey="Rogelj B">B Rogelj</name>
</author>
<author><name sortKey="Hortobagyi, T" uniqKey="Hortobagyi T">T Hortobagyi</name>
</author>
<author><name sortKey="De Vos, Kj" uniqKey="De Vos K">KJ De Vos</name>
</author>
<author><name sortKey="Nishimura, Al" uniqKey="Nishimura A">AL Nishimura</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Baker, M" uniqKey="Baker M">M Baker</name>
</author>
<author><name sortKey="Mackenzie, Ir" uniqKey="Mackenzie I">IR Mackenzie</name>
</author>
<author><name sortKey="Pickering Brown, Sm" uniqKey="Pickering Brown S">SM Pickering-Brown</name>
</author>
<author><name sortKey="Gass, J" uniqKey="Gass J">J Gass</name>
</author>
<author><name sortKey="Rademakers, R" uniqKey="Rademakers R">R Rademakers</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Cruts, M" uniqKey="Cruts M">M Cruts</name>
</author>
<author><name sortKey="Gijselinck, I" uniqKey="Gijselinck I">I Gijselinck</name>
</author>
<author><name sortKey="Van Der Zee, J" uniqKey="Van Der Zee J">J van der Zee</name>
</author>
<author><name sortKey="Engelborghs, S" uniqKey="Engelborghs S">S Engelborghs</name>
</author>
<author><name sortKey="Wils, H" uniqKey="Wils H">H Wils</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Hutton, M" uniqKey="Hutton M">M Hutton</name>
</author>
<author><name sortKey="Lendon, Cl" uniqKey="Lendon C">CL Lendon</name>
</author>
<author><name sortKey="Rizzu, P" uniqKey="Rizzu P">P Rizzu</name>
</author>
<author><name sortKey="Baker, M" uniqKey="Baker M">M Baker</name>
</author>
<author><name sortKey="Froelich, S" uniqKey="Froelich S">S Froelich</name>
</author>
</analytic>
</biblStruct>
<biblStruct></biblStruct>
<biblStruct><analytic><author><name sortKey="Bottomley, Rh" uniqKey="Bottomley R">RH Bottomley</name>
</author>
<author><name sortKey="Trainer, Al" uniqKey="Trainer A">AL Trainer</name>
</author>
<author><name sortKey="Griffin, Mj" uniqKey="Griffin M">MJ Griffin</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Falkenburger, Bh" uniqKey="Falkenburger B">BH Falkenburger</name>
</author>
<author><name sortKey="Schulz, Jb" uniqKey="Schulz J">JB Schulz</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Gibbs, Jr" uniqKey="Gibbs J">JR Gibbs</name>
</author>
<author><name sortKey="Singleton, A" uniqKey="Singleton A">A Singleton</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Yu, J" uniqKey="Yu J">J Yu</name>
</author>
<author><name sortKey="Vodyanik, Ma" uniqKey="Vodyanik M">MA Vodyanik</name>
</author>
<author><name sortKey="Smuga Otto, K" uniqKey="Smuga Otto K">K Smuga-Otto</name>
</author>
<author><name sortKey="Antosiewicz Bourget, J" uniqKey="Antosiewicz Bourget J">J Antosiewicz-Bourget</name>
</author>
<author><name sortKey="Frane, Jl" uniqKey="Frane J">JL Frane</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Takahashi, K" uniqKey="Takahashi K">K Takahashi</name>
</author>
<author><name sortKey="Tanabe, K" uniqKey="Tanabe K">K Tanabe</name>
</author>
<author><name sortKey="Ohnuki, M" uniqKey="Ohnuki M">M Ohnuki</name>
</author>
<author><name sortKey="Narita, M" uniqKey="Narita M">M Narita</name>
</author>
<author><name sortKey="Ichisaka, T" uniqKey="Ichisaka T">T Ichisaka</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Park, Ih" uniqKey="Park I">IH Park</name>
</author>
<author><name sortKey="Zhao, R" uniqKey="Zhao R">R Zhao</name>
</author>
<author><name sortKey="West, Ja" uniqKey="West J">JA West</name>
</author>
<author><name sortKey="Yabuuchi, A" uniqKey="Yabuuchi A">A Yabuuchi</name>
</author>
<author><name sortKey="Huo, H" uniqKey="Huo H">H Huo</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Devine, Mj" uniqKey="Devine M">MJ Devine</name>
</author>
<author><name sortKey="Ryten, M" uniqKey="Ryten M">M Ryten</name>
</author>
<author><name sortKey="Vodicka, P" uniqKey="Vodicka P">P Vodicka</name>
</author>
<author><name sortKey="Thomson, Aj" uniqKey="Thomson A">AJ Thomson</name>
</author>
<author><name sortKey="Burdon, T" uniqKey="Burdon T">T Burdon</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Dimos, Jt" uniqKey="Dimos J">JT Dimos</name>
</author>
<author><name sortKey="Rodolfa, Kt" uniqKey="Rodolfa K">KT Rodolfa</name>
</author>
<author><name sortKey="Niakan, Kk" uniqKey="Niakan K">KK Niakan</name>
</author>
<author><name sortKey="Weisenthal, Lm" uniqKey="Weisenthal L">LM Weisenthal</name>
</author>
<author><name sortKey="Mitsumoto, H" uniqKey="Mitsumoto H">H Mitsumoto</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Koch, P" uniqKey="Koch P">P Koch</name>
</author>
<author><name sortKey="Breuer, P" uniqKey="Breuer P">P Breuer</name>
</author>
<author><name sortKey="Peitz, M" uniqKey="Peitz M">M Peitz</name>
</author>
<author><name sortKey="Jungverdorben, J" uniqKey="Jungverdorben J">J Jungverdorben</name>
</author>
<author><name sortKey="Kesavan, J" uniqKey="Kesavan J">J Kesavan</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Qiang, L" uniqKey="Qiang L">L Qiang</name>
</author>
<author><name sortKey="Fujita, R" uniqKey="Fujita R">R Fujita</name>
</author>
<author><name sortKey="Yamashita, T" uniqKey="Yamashita T">T Yamashita</name>
</author>
<author><name sortKey="Angulo, S" uniqKey="Angulo S">S Angulo</name>
</author>
<author><name sortKey="Rhinn, H" uniqKey="Rhinn H">H Rhinn</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Cooper, O" uniqKey="Cooper O">O Cooper</name>
</author>
<author><name sortKey="Seo, H" uniqKey="Seo H">H Seo</name>
</author>
<author><name sortKey="Andrabi, S" uniqKey="Andrabi S">S Andrabi</name>
</author>
<author><name sortKey="Guardia Laguarta, C" uniqKey="Guardia Laguarta C">C Guardia-Laguarta</name>
</author>
<author><name sortKey="Graziotto, J" uniqKey="Graziotto J">J Graziotto</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Shi, Y" uniqKey="Shi Y">Y Shi</name>
</author>
<author><name sortKey="Kirwan, P" uniqKey="Kirwan P">P Kirwan</name>
</author>
<author><name sortKey="Smith, J" uniqKey="Smith J">J Smith</name>
</author>
<author><name sortKey="Maclean, G" uniqKey="Maclean G">G Maclean</name>
</author>
<author><name sortKey="Orkin, Sh" uniqKey="Orkin S">SH Orkin</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Israel, Ma" uniqKey="Israel M">MA Israel</name>
</author>
<author><name sortKey="Yuan, Sh" uniqKey="Yuan S">SH Yuan</name>
</author>
<author><name sortKey="Bardy, C" uniqKey="Bardy C">C Bardy</name>
</author>
<author><name sortKey="Reyna, Sm" uniqKey="Reyna S">SM Reyna</name>
</author>
<author><name sortKey="Mu, Y" uniqKey="Mu Y">Y Mu</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Cherry, Ab" uniqKey="Cherry A">AB Cherry</name>
</author>
<author><name sortKey="Daley, Gq" uniqKey="Daley G">GQ Daley</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Strutz, F" uniqKey="Strutz F">F Strutz</name>
</author>
<author><name sortKey="Okada, H" uniqKey="Okada H">H Okada</name>
</author>
<author><name sortKey="Lo, Cw" uniqKey="Lo C">CW Lo</name>
</author>
<author><name sortKey="Danoff, T" uniqKey="Danoff T">T Danoff</name>
</author>
<author><name sortKey="Carone, Rl" uniqKey="Carone R">RL Carone</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Park, Ih" uniqKey="Park I">IH Park</name>
</author>
<author><name sortKey="Arora, N" uniqKey="Arora N">N Arora</name>
</author>
<author><name sortKey="Huo, H" uniqKey="Huo H">H Huo</name>
</author>
<author><name sortKey="Maherali, N" uniqKey="Maherali N">N Maherali</name>
</author>
<author><name sortKey="Ahfeldt, T" uniqKey="Ahfeldt T">T Ahfeldt</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Campion, D" uniqKey="Campion D">D Campion</name>
</author>
<author><name sortKey="Flaman, Jm" uniqKey="Flaman J">JM Flaman</name>
</author>
<author><name sortKey="Brice, A" uniqKey="Brice A">A Brice</name>
</author>
<author><name sortKey="Hannequin, D" uniqKey="Hannequin D">D Hannequin</name>
</author>
<author><name sortKey="Dubois, B" uniqKey="Dubois B">B Dubois</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Jorgensen, P" uniqKey="Jorgensen P">P Jorgensen</name>
</author>
<author><name sortKey="Bus, C" uniqKey="Bus C">C Bus</name>
</author>
<author><name sortKey="Pallisgaard, N" uniqKey="Pallisgaard N">N Pallisgaard</name>
</author>
<author><name sortKey="Bryder, M" uniqKey="Bryder M">M Bryder</name>
</author>
<author><name sortKey="Jorgensen, Al" uniqKey="Jorgensen A">AL Jorgensen</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Janssen, Jc" uniqKey="Janssen J">JC Janssen</name>
</author>
<author><name sortKey="Beck, Ja" uniqKey="Beck J">JA Beck</name>
</author>
<author><name sortKey="Campbell, Ta" uniqKey="Campbell T">TA Campbell</name>
</author>
<author><name sortKey="Dickinson, A" uniqKey="Dickinson A">A Dickinson</name>
</author>
<author><name sortKey="Fox, Nc" uniqKey="Fox N">NC Fox</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Godbolt, Ak" uniqKey="Godbolt A">AK Godbolt</name>
</author>
<author><name sortKey="Beck, Ja" uniqKey="Beck J">JA Beck</name>
</author>
<author><name sortKey="Collinge, J" uniqKey="Collinge J">J Collinge</name>
</author>
<author><name sortKey="Garrard, P" uniqKey="Garrard P">P Garrard</name>
</author>
<author><name sortKey="Warren, Jd" uniqKey="Warren J">JD Warren</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Gwinn, K" uniqKey="Gwinn K">K Gwinn</name>
</author>
<author><name sortKey="Devine, Mj" uniqKey="Devine M">MJ Devine</name>
</author>
<author><name sortKey="Jin, Lw" uniqKey="Jin L">LW Jin</name>
</author>
<author><name sortKey="Johnson, J" uniqKey="Johnson J">J Johnson</name>
</author>
<author><name sortKey="Bird, T" uniqKey="Bird T">T Bird</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Wszolek, Zk" uniqKey="Wszolek Z">ZK Wszolek</name>
</author>
<author><name sortKey="Pfeiffer, B" uniqKey="Pfeiffer B">B Pfeiffer</name>
</author>
<author><name sortKey="Fulgham, Jr" uniqKey="Fulgham J">JR Fulgham</name>
</author>
<author><name sortKey="Parisi, Je" uniqKey="Parisi J">JE Parisi</name>
</author>
<author><name sortKey="Thompson, Bm" uniqKey="Thompson B">BM Thompson</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Zimprich, A" uniqKey="Zimprich A">A Zimprich</name>
</author>
<author><name sortKey="Biskup, S" uniqKey="Biskup S">S Biskup</name>
</author>
<author><name sortKey="Leitner, P" uniqKey="Leitner P">P Leitner</name>
</author>
<author><name sortKey="Lichtner, P" uniqKey="Lichtner P">P Lichtner</name>
</author>
<author><name sortKey="Farrer, M" uniqKey="Farrer M">M Farrer</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Healy, Dg" uniqKey="Healy D">DG Healy</name>
</author>
<author><name sortKey="Falchi, M" uniqKey="Falchi M">M Falchi</name>
</author>
<author><name sortKey="O Sullivan, Ss" uniqKey="O Sullivan S">SS O'Sullivan</name>
</author>
<author><name sortKey="Bonifati, V" uniqKey="Bonifati V">V Bonifati</name>
</author>
<author><name sortKey="Durr, A" uniqKey="Durr A">A Durr</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Clark, Ln" uniqKey="Clark L">LN Clark</name>
</author>
<author><name sortKey="Wang, Y" uniqKey="Wang Y">Y Wang</name>
</author>
<author><name sortKey="Karlins, E" uniqKey="Karlins E">E Karlins</name>
</author>
<author><name sortKey="Saito, L" uniqKey="Saito L">L Saito</name>
</author>
<author><name sortKey="Mejia Santana, H" uniqKey="Mejia Santana H">H Mejia-Santana</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Alcalay, Rn" uniqKey="Alcalay R">RN Alcalay</name>
</author>
<author><name sortKey="Caccappolo, E" uniqKey="Caccappolo E">E Caccappolo</name>
</author>
<author><name sortKey="Mejia Santana, H" uniqKey="Mejia Santana H">H Mejia-Santana</name>
</author>
<author><name sortKey="Tang, Mx" uniqKey="Tang M">MX Tang</name>
</author>
<author><name sortKey="Rosado, L" uniqKey="Rosado L">L Rosado</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Ishihara, L" uniqKey="Ishihara L">L Ishihara</name>
</author>
<author><name sortKey="Warren, L" uniqKey="Warren L">L Warren</name>
</author>
<author><name sortKey="Gibson, R" uniqKey="Gibson R">R Gibson</name>
</author>
<author><name sortKey="Amouri, R" uniqKey="Amouri R">R Amouri</name>
</author>
<author><name sortKey="Lesage, S" uniqKey="Lesage S">S Lesage</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Clark, Ln" uniqKey="Clark L">LN Clark</name>
</author>
<author><name sortKey="Ross, Bm" uniqKey="Ross B">BM Ross</name>
</author>
<author><name sortKey="Wang, Y" uniqKey="Wang Y">Y Wang</name>
</author>
<author><name sortKey="Mejia Santana, H" uniqKey="Mejia Santana H">H Mejia-Santana</name>
</author>
<author><name sortKey="Harris, J" uniqKey="Harris J">J Harris</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Marder, Ks" uniqKey="Marder K">KS Marder</name>
</author>
<author><name sortKey="Tang, Mx" uniqKey="Tang M">MX Tang</name>
</author>
<author><name sortKey="Mejia Santana, H" uniqKey="Mejia Santana H">H Mejia-Santana</name>
</author>
<author><name sortKey="Rosado, L" uniqKey="Rosado L">L Rosado</name>
</author>
<author><name sortKey="Louis, Ed" uniqKey="Louis E">ED Louis</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Clark, Ln" uniqKey="Clark L">LN Clark</name>
</author>
<author><name sortKey="Haamer, E" uniqKey="Haamer E">E Haamer</name>
</author>
<author><name sortKey="Mejia Santana, H" uniqKey="Mejia Santana H">H Mejia-Santana</name>
</author>
<author><name sortKey="Harris, J" uniqKey="Harris J">J Harris</name>
</author>
<author><name sortKey="Lesage, S" uniqKey="Lesage S">S Lesage</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Puschmann, A" uniqKey="Puschmann A">A Puschmann</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Narozanska, E" uniqKey="Narozanska E">E Narozanska</name>
</author>
<author><name sortKey="Jasinska Myga, B" uniqKey="Jasinska Myga B">B Jasinska-Myga</name>
</author>
<author><name sortKey="Sitek, Ej" uniqKey="Sitek E">EJ Sitek</name>
</author>
<author><name sortKey="Robowski, P" uniqKey="Robowski P">P Robowski</name>
</author>
<author><name sortKey="Brockhuis, B" uniqKey="Brockhuis B">B Brockhuis</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Whitwell, Jl" uniqKey="Whitwell J">JL Whitwell</name>
</author>
<author><name sortKey="Jack, Cr" uniqKey="Jack C">CR Jack</name>
</author>
<author><name sortKey="Boeve, Bf" uniqKey="Boeve B">BF Boeve</name>
</author>
<author><name sortKey="Senjem, Ml" uniqKey="Senjem M">ML Senjem</name>
</author>
<author><name sortKey="Baker, M" uniqKey="Baker M">M Baker</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Wszolek, Zk" uniqKey="Wszolek Z">ZK Wszolek</name>
</author>
<author><name sortKey="Pfeiffer, Rf" uniqKey="Pfeiffer R">RF Pfeiffer</name>
</author>
<author><name sortKey="Bhatt, Mh" uniqKey="Bhatt M">MH Bhatt</name>
</author>
<author><name sortKey="Schelper, Rl" uniqKey="Schelper R">RL Schelper</name>
</author>
<author><name sortKey="Cordes, M" uniqKey="Cordes M">M Cordes</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Tsuboi, Y" uniqKey="Tsuboi Y">Y Tsuboi</name>
</author>
<author><name sortKey="Baker, M" uniqKey="Baker M">M Baker</name>
</author>
<author><name sortKey="Hutton, Ml" uniqKey="Hutton M">ML Hutton</name>
</author>
<author><name sortKey="Uitti, Rj" uniqKey="Uitti R">RJ Uitti</name>
</author>
<author><name sortKey="Rascol, O" uniqKey="Rascol O">O Rascol</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Janssen, Jc" uniqKey="Janssen J">JC Janssen</name>
</author>
<author><name sortKey="Warrington, Ek" uniqKey="Warrington E">EK Warrington</name>
</author>
<author><name sortKey="Morris, Hr" uniqKey="Morris H">HR Morris</name>
</author>
<author><name sortKey="Lantos, P" uniqKey="Lantos P">P Lantos</name>
</author>
<author><name sortKey="Brown, J" uniqKey="Brown J">J Brown</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Kantarci, K" uniqKey="Kantarci K">K Kantarci</name>
</author>
<author><name sortKey="Boeve, Bf" uniqKey="Boeve B">BF Boeve</name>
</author>
<author><name sortKey="Wszolek, Zk" uniqKey="Wszolek Z">ZK Wszolek</name>
</author>
<author><name sortKey="Rademakers, R" uniqKey="Rademakers R">R Rademakers</name>
</author>
<author><name sortKey="Whitwell, Jl" uniqKey="Whitwell J">JL Whitwell</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Gass, J" uniqKey="Gass J">J Gass</name>
</author>
<author><name sortKey="Cannon, A" uniqKey="Cannon A">A Cannon</name>
</author>
<author><name sortKey="Mackenzie, Ir" uniqKey="Mackenzie I">IR Mackenzie</name>
</author>
<author><name sortKey="Boeve, B" uniqKey="Boeve B">B Boeve</name>
</author>
<author><name sortKey="Baker, M" uniqKey="Baker M">M Baker</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Rohrer, Jd" uniqKey="Rohrer J">JD Rohrer</name>
</author>
<author><name sortKey="Guerreiro, R" uniqKey="Guerreiro R">R Guerreiro</name>
</author>
<author><name sortKey="Vandrovcova, J" uniqKey="Vandrovcova J">J Vandrovcova</name>
</author>
<author><name sortKey="Uphill, J" uniqKey="Uphill J">J Uphill</name>
</author>
<author><name sortKey="Reiman, D" uniqKey="Reiman D">D Reiman</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Miller, Td" uniqKey="Miller T">TD Miller</name>
</author>
<author><name sortKey="Jackson, Ap" uniqKey="Jackson A">AP Jackson</name>
</author>
<author><name sortKey="Barresi, R" uniqKey="Barresi R">R Barresi</name>
</author>
<author><name sortKey="Smart, Cm" uniqKey="Smart C">CM Smart</name>
</author>
<author><name sortKey="Eugenicos, M" uniqKey="Eugenicos M">M Eugenicos</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Farrer, Mj" uniqKey="Farrer M">MJ Farrer</name>
</author>
<author><name sortKey="Hulihan, Mm" uniqKey="Hulihan M">MM Hulihan</name>
</author>
<author><name sortKey="Kachergus, Jm" uniqKey="Kachergus J">JM Kachergus</name>
</author>
<author><name sortKey="Dachsel, Jc" uniqKey="Dachsel J">JC Dachsel</name>
</author>
<author><name sortKey="Stoessl, Aj" uniqKey="Stoessl A">AJ Stoessl</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Wider, C" uniqKey="Wider C">C Wider</name>
</author>
<author><name sortKey="Dickson, Dw" uniqKey="Dickson D">DW Dickson</name>
</author>
<author><name sortKey="Stoessl, Aj" uniqKey="Stoessl A">AJ Stoessl</name>
</author>
<author><name sortKey="Tsuboi, Y" uniqKey="Tsuboi Y">Y Tsuboi</name>
</author>
<author><name sortKey="Chapon, F" uniqKey="Chapon F">F Chapon</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Van Gerpen, Ja" uniqKey="Van Gerpen J">JA Van Gerpen</name>
</author>
<author><name sortKey="Ledoux, Ms" uniqKey="Ledoux M">MS Ledoux</name>
</author>
<author><name sortKey="Wszolek, Zk" uniqKey="Wszolek Z">ZK Wszolek</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Ledoux, Ms" uniqKey="Ledoux M">MS Ledoux</name>
</author>
<author><name sortKey="Xiao, J" uniqKey="Xiao J">J Xiao</name>
</author>
<author><name sortKey="Rudzinska, M" uniqKey="Rudzinska M">M Rudzinska</name>
</author>
<author><name sortKey="Bastian, Rw" uniqKey="Bastian R">RW Bastian</name>
</author>
<author><name sortKey="Wszolek, Zk" uniqKey="Wszolek Z">ZK Wszolek</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Hayflick, L" uniqKey="Hayflick L">L Hayflick</name>
</author>
<author><name sortKey="Moorhead, Ps" uniqKey="Moorhead P">PS Moorhead</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Kitada, M" uniqKey="Kitada M">M Kitada</name>
</author>
<author><name sortKey="Wakao, S" uniqKey="Wakao S">S Wakao</name>
</author>
<author><name sortKey="Dezawa, M" uniqKey="Dezawa M">M Dezawa</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Wakao, S" uniqKey="Wakao S">S Wakao</name>
</author>
<author><name sortKey="Kitada, M" uniqKey="Kitada M">M Kitada</name>
</author>
<author><name sortKey="Kuroda, Y" uniqKey="Kuroda Y">Y Kuroda</name>
</author>
<author><name sortKey="Shigemoto, T" uniqKey="Shigemoto T">T Shigemoto</name>
</author>
<author><name sortKey="Matsuse, D" uniqKey="Matsuse D">D Matsuse</name>
</author>
</analytic>
</biblStruct>
<biblStruct><analytic><author><name sortKey="Feng, B" uniqKey="Feng B">B Feng</name>
</author>
<author><name sortKey="Ng, Jh" uniqKey="Ng J">JH Ng</name>
</author>
<author><name sortKey="Heng, Jc" uniqKey="Heng J">JC Heng</name>
</author>
<author><name sortKey="Ng, Hh" uniqKey="Ng H">HH Ng</name>
</author>
</analytic>
</biblStruct>
</listBibl>
</div1>
</back>
</TEI>
<pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">PLoS One</journal-id>
<journal-id journal-id-type="iso-abbrev">PLoS ONE</journal-id>
<journal-id journal-id-type="publisher-id">plos</journal-id>
<journal-id journal-id-type="pmc">plosone</journal-id>
<journal-title-group><journal-title>PLoS ONE</journal-title>
</journal-title-group>
<issn pub-type="epub">1932-6203</issn>
<publisher><publisher-name>Public Library of Science</publisher-name>
<publisher-loc>San Francisco, USA</publisher-loc>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">22952635</article-id>
<article-id pub-id-type="pmc">3428297</article-id>
<article-id pub-id-type="publisher-id">PONE-D-11-13292</article-id>
<article-id pub-id-type="doi">10.1371/journal.pone.0043099</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject>
</subj-group>
<subj-group subj-group-type="Discipline-v2"><subject>Biology</subject>
<subj-group><subject>Neuroscience</subject>
<subj-group><subject>Molecular Neuroscience</subject>
<subject>Neurobiology of Disease and Regeneration</subject>
</subj-group>
</subj-group>
</subj-group>
<subj-group subj-group-type="Discipline-v2"><subject>Medicine</subject>
<subj-group><subject>Clinical Genetics</subject>
<subj-group><subject>Autosomal Dominant</subject>
</subj-group>
</subj-group>
<subj-group><subject>Neurology</subject>
<subj-group><subject>Dementia</subject>
<subj-group><subject>Alzheimer Disease</subject>
</subj-group>
</subj-group>
<subj-group><subject>Motor Neuron Diseases</subject>
<subject>Parkinson Disease</subject>
</subj-group>
</subj-group>
</subj-group>
</article-categories>
<title-group><article-title>Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research</article-title>
<alt-title alt-title-type="running-head">A Fibroblast Resource for Disease Research</alt-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Wray</surname>
<given-names>Selina</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Self</surname>
<given-names>Matthew</given-names>
</name>
<xref ref-type="aff" rid="aff2"><sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author"><collab>NINDS Parkinson's Disease iPSC Consortium</collab>
<xref ref-type="aff" rid="aff25"><sup>25</sup>
</xref>
</contrib>
<contrib contrib-type="author"><collab>NINDS Huntington's Disease iPSC Consortium</collab>
<xref ref-type="aff" rid="aff25"><sup>25</sup>
</xref>
</contrib>
<contrib contrib-type="author"><collab>NINDS ALS iPSC Consortium</collab>
<xref ref-type="aff" rid="aff25"><sup>25</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Lewis</surname>
<given-names>Patrick A.</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Taanman</surname>
<given-names>Jan-Willem</given-names>
</name>
<xref ref-type="aff" rid="aff4"><sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Ryan</surname>
<given-names>Natalie S.</given-names>
</name>
<xref ref-type="aff" rid="aff3"><sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Mahoney</surname>
<given-names>Colin J.</given-names>
</name>
<xref ref-type="aff" rid="aff3"><sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Liang</surname>
<given-names>Yuying</given-names>
</name>
<xref ref-type="aff" rid="aff3"><sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Devine</surname>
<given-names>Michael J.</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Sheerin</surname>
<given-names>Una-Marie</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Houlden</surname>
<given-names>Henry</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Morris</surname>
<given-names>Huw R.</given-names>
</name>
<xref ref-type="aff" rid="aff5"><sup>5</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Healy</surname>
<given-names>Daniel</given-names>
</name>
<xref ref-type="aff" rid="aff4"><sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Marti-Masso</surname>
<given-names>Jose-Felix</given-names>
</name>
<xref ref-type="aff" rid="aff6"><sup>6</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Preza</surname>
<given-names>Elisavet</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Barker</surname>
<given-names>Suzanne</given-names>
</name>
<xref ref-type="aff" rid="aff3"><sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Sutherland</surname>
<given-names>Margaret</given-names>
</name>
<xref ref-type="aff" rid="aff7"><sup>7</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Corriveau</surname>
<given-names>Roderick A.</given-names>
</name>
<xref ref-type="aff" rid="aff7"><sup>7</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>D'Andrea</surname>
<given-names>Michael</given-names>
</name>
<xref ref-type="aff" rid="aff2"><sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Schapira</surname>
<given-names>Anthony H. V.</given-names>
</name>
<xref ref-type="aff" rid="aff4"><sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Uitti</surname>
<given-names>Ryan J.</given-names>
</name>
<xref ref-type="aff" rid="aff8"><sup>8</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Guttman</surname>
<given-names>Mark</given-names>
</name>
<xref ref-type="aff" rid="aff9"><sup>9</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Opala</surname>
<given-names>Grzegorz</given-names>
</name>
<xref ref-type="aff" rid="aff10"><sup>10</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Jasinska-Myga</surname>
<given-names>Barbara</given-names>
</name>
<xref ref-type="aff" rid="aff10"><sup>10</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Puschmann</surname>
<given-names>Andreas</given-names>
</name>
<xref ref-type="aff" rid="aff11"><sup>11</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Nilsson</surname>
<given-names>Christer</given-names>
</name>
<xref ref-type="aff" rid="aff11"><sup>11</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Espay</surname>
<given-names>Alberto J.</given-names>
</name>
<xref ref-type="aff" rid="aff12"><sup>12</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Slawek</surname>
<given-names>Jaroslaw</given-names>
</name>
<xref ref-type="aff" rid="aff13"><sup>13</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Gutmann</surname>
<given-names>Ludwig</given-names>
</name>
<xref ref-type="aff" rid="aff14"><sup>14</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Boeve</surname>
<given-names>Bradley F.</given-names>
</name>
<xref ref-type="aff" rid="aff15"><sup>15</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Boylan</surname>
<given-names>Kevin</given-names>
</name>
<xref ref-type="aff" rid="aff8"><sup>8</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Stoessl</surname>
<given-names>A. Jon</given-names>
</name>
<xref ref-type="aff" rid="aff16"><sup>16</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Ross</surname>
<given-names>Owen A.</given-names>
</name>
<xref ref-type="aff" rid="aff8"><sup>8</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Maragakis</surname>
<given-names>Nicholas J.</given-names>
</name>
<xref ref-type="aff" rid="aff17"><sup>17</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Van Gerpen</surname>
<given-names>Jay</given-names>
</name>
<xref ref-type="aff" rid="aff8"><sup>8</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Gerstenhaber</surname>
<given-names>Melissa</given-names>
</name>
<xref ref-type="aff" rid="aff18"><sup>18</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Gwinn</surname>
<given-names>Katrina</given-names>
</name>
<xref ref-type="aff" rid="aff23"><sup>23</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Dawson</surname>
<given-names>Ted M.</given-names>
</name>
<xref ref-type="aff" rid="aff19"><sup>19</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Isacson</surname>
<given-names>Ole</given-names>
</name>
<xref ref-type="aff" rid="aff20"><sup>20</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Marder</surname>
<given-names>Karen S.</given-names>
</name>
<xref ref-type="aff" rid="aff21"><sup>21</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Clark</surname>
<given-names>Lorraine N.</given-names>
</name>
<xref ref-type="aff" rid="aff21"><sup>21</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Przedborski</surname>
<given-names>Serge E.</given-names>
</name>
<xref ref-type="aff" rid="aff22"><sup>22</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Finkbeiner</surname>
<given-names>Steven</given-names>
</name>
<xref ref-type="aff" rid="aff24"><sup>24</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Rothstein</surname>
<given-names>Jeffrey D.</given-names>
</name>
<xref ref-type="aff" rid="aff18"><sup>18</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Wszolek</surname>
<given-names>Zbigniew K.</given-names>
</name>
<xref ref-type="aff" rid="aff8"><sup>8</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Rossor</surname>
<given-names>Martin N.</given-names>
</name>
<xref ref-type="aff" rid="aff3"><sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Hardy</surname>
<given-names>John</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup>
</xref>
<xref ref-type="corresp" rid="cor1"><sup>*</sup>
</xref>
</contrib>
</contrib-group>
<aff id="aff1"><label>1</label>
<addr-line>Department of Molecular Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</aff>
<aff id="aff2"><label>2</label>
<addr-line>Coriell Institute for Medical Research, Camden, New Jersey, United States of America</addr-line>
</aff>
<aff id="aff3"><label>3</label>
<addr-line>Dementia Research Centre, Department of Neurodegenerative Diseases, University College London Institute of Neurology, London, United Kingdom</addr-line>
</aff>
<aff id="aff4"><label>4</label>
<addr-line>Department of Clinical Neuroscience, University College London Institute of Neurology, London, United Kingdom</addr-line>
</aff>
<aff id="aff5"><label>5</label>
<addr-line>Cardiff University School of Medicine, University of Cardiff, Cardiff, United Kingdom</addr-line>
</aff>
<aff id="aff6"><label>6</label>
<addr-line>Hospital Donastia, San Sebastian, Spain</addr-line>
</aff>
<aff id="aff7"><label>7</label>
<addr-line>National Institute for Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, United States of America</addr-line>
</aff>
<aff id="aff8"><label>8</label>
<addr-line>Departments of Neurology and Neuroscience, Mayo Clinic Jacksonville, Jacksonville, Florida, United States of America</addr-line>
</aff>
<aff id="aff9"><label>9</label>
<addr-line>Department of Neurology, Center for Movement Disorders, Ontario, Canada</addr-line>
</aff>
<aff id="aff10"><label>10</label>
<addr-line>Department of Neurology, Medical University of Silesia, Katowice, Poland</addr-line>
</aff>
<aff id="aff11"><label>11</label>
<addr-line>Department of Geriatric Psychiatry, Lund University, Lund, Sweden</addr-line>
</aff>
<aff id="aff12"><label>12</label>
<addr-line>Department of Neurology, University of Cincinnati, Cincinnati, Ohio, United States of America</addr-line>
</aff>
<aff id="aff13"><label>13</label>
<addr-line>Department of Neurological and Psychiatric Nursing, Medical University of Gdansk, Gdansk, Poland</addr-line>
</aff>
<aff id="aff14"><label>14</label>
<addr-line>Department of Neurology , West Virginia University, West Virginia, United States of America</addr-line>
</aff>
<aff id="aff15"><label>15</label>
<addr-line>Department of Neurology, Mayo Clinic, Rochester, Minnesota, United States of America</addr-line>
</aff>
<aff id="aff16"><label>16</label>
<addr-line>Division of Neurology, Pacific Parkinson's Research Centre, University of British Columbia, Vancouver, British Columbia, Canada</addr-line>
</aff>
<aff id="aff17"><label>17</label>
<addr-line>Department of Neurology and Neuroscience, School of Medicine, Johns Hopkins University, Baltimore, Maryland, United States of America</addr-line>
</aff>
<aff id="aff18"><label>18</label>
<addr-line>Department of Psychiatry and Behavioural Sciences, John Hopkins University School of Medicine, Baltimore, Maryland, United States of America</addr-line>
</aff>
<aff id="aff19"><label>19</label>
<addr-line>Neuroregeneration Program, Institute of Cell Engineering, Department of Neurology and the Solomon H. Snyder Department of Neuroscience, John Hopkins University, Baltimore, Maryland, United States of America</addr-line>
</aff>
<aff id="aff20"><label>20</label>
<addr-line>Center for Neuroregeneration Research, Harvard Medical School, Belmont, Massachusetts, United States of America</addr-line>
</aff>
<aff id="aff21"><label>21</label>
<addr-line>Department of Neurology, Psychiatry, Sergievsky Center, and Taub Institute, College of Physicians and Surgeons, Columbia University, New York, New York, United States of America</addr-line>
</aff>
<aff id="aff22"><label>22</label>
<addr-line>Center for Motor Neuron Biology and Diseases, Departments of Neurology, Pathology and Cell Biology, College of Physicians and Surgeons, Columbia University, New York, New York, United States of America</addr-line>
</aff>
<aff id="aff23"><label>23</label>
<addr-line>Baylor College of Medicine, Department of Genetics, Houston, Texas, United States of America</addr-line>
</aff>
<aff id="aff24"><label>24</label>
<addr-line>Gladstone Institute of Neurological Disease, Taube-Koret Center for Huntington's Disease Research, Departments of Neurology and Physiology, University of California San Francisco, San Francisco, California, United States of America</addr-line>
</aff>
<aff id="aff25"><label>25</label>
<addr-line>For a full list of the members of the NINDS Parkinson's Disease iPSC Consortium, NINDS Huntington's Disease iPSC Consortium, and NINDS ALS iPSC Consortium please see the Acknowledgments section</addr-line>
</aff>
<contrib-group><contrib contrib-type="editor"><name><surname>Borlongan</surname>
<given-names>Cesar V.</given-names>
</name>
<role>Editor</role>
<xref ref-type="aff" rid="edit1"></xref>
</contrib>
</contrib-group>
<aff id="edit1"><addr-line>University of South Florida, United States of America</addr-line>
</aff>
<author-notes><corresp id="cor1">* E-mail: <email>j.hardy@ucl.ac.uk</email>
</corresp>
<fn fn-type="conflict"><p><bold>Competing Interests: </bold>
The authors have declared that no competing interests exist.</p>
</fn>
<fn fn-type="con"><p>Conceived and designed the experiments: JH MNR ZKW TMD KSM OI KG M. Self M. Sutherland SB. Performed the experiments: SW M. Self PAL JWT EP MJD LNC OAR. Analyzed the data: SW M. Self PAL JWT EP MJD LNC OAR. Contributed reagents/materials/analysis tools: NSR CJM UMS HH HRM DH JFMM AHVS RJU M. Guttman M. Gerstenhaber GO BJM AP CN AJE JS LG BB KB AJS NJM JVG TMD OI KSM SP SF JDR ZKW MNR YL. Wrote the paper: SW JH. Project management at NINDS repository: M. Sutherland RAC MD KG.</p>
</fn>
</author-notes>
<pub-date pub-type="collection"><year>2012</year>
</pub-date>
<pub-date pub-type="epub"><day>27</day>
<month>8</month>
<year>2012</year>
</pub-date>
<volume>7</volume>
<issue>8</issue>
<elocation-id>e43099</elocation-id>
<history><date date-type="received"><day>12</day>
<month>7</month>
<year>2011</year>
</date>
<date date-type="accepted"><day>19</day>
<month>7</month>
<year>2012</year>
</date>
</history>
<permissions><copyright-year>2012</copyright-year>
<license><license-p>This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.</license-p>
</license>
</permissions>
<abstract><p>Our understanding of the molecular mechanisms of many neurological disorders has been greatly enhanced by the discovery of mutations in genes linked to familial forms of these diseases. These have facilitated the generation of cell and animal models that can be used to understand the underlying molecular pathology. Recently, there has been a surge of interest in the use of patient-derived cells, due to the development of induced pluripotent stem cells and their subsequent differentiation into neurons and glia. Access to patient cell lines carrying the relevant mutations is a limiting factor for many centres wishing to pursue this research. We have therefore generated an open-access collection of fibroblast lines from patients carrying mutations linked to neurological disease. These cell lines have been deposited in the National Institute for Neurological Disorders and Stroke (NINDS) Repository at the Coriell Institute for Medical Research and can be requested by any research group for use in <italic>in vitro</italic>
disease modelling. There are currently 71 mutation-defined cell lines available for request from a wide range of neurological disorders and this collection will be continually expanded. This represents a significant resource that will advance the use of patient cells as disease models by the scientific community.</p>
</abstract>
<funding-group><funding-statement>This work was supported by the following grants and funding agencies: Alzheimer's Research UK (SW and JH), The Alzheimer's Society (MNR), Parkinson's UK (PAL and JH), the Medical Research Council, the National Institute of Neurological Disorders and Stroke (National Institute of Neurological Disorders and Stroke/National Institutes of Health grants NS38377 [TD], NS060113 [LNC], NS036630 [KSM], NS050487 [LNC]), GO grants RC2NS069395, RC2NS069422, RC2 NS070276, Mayo Clinic Morris K. Udall Center grants P50NS072187 and P50 NS072187-01S2 (ZKW, RJU, OAR), Columbia Udall grant P50NS38370 (SP), MDSCF grant 2007-MSCRFI-0420-00 (TD), P2ALS (JDR), The Parkinson's Disease Foundation (LNC, SP, KSM), The Swedish Parkinson Academy (AP and CN) and the Michael J. Fox Foundation (JH, KSM, LNC). This work was partly undertaken at University College London Hospitals/University College London (UCL), which receives a proportion of funding from the Department of Health's National Institute for Health Research Biomedical Research Centres funding scheme. This work was also supported in part by the Wellcome Trust/Medical Research Council (MRC) Joint Call in Neurodegeneration award (WT089698) to the UK Parkinson's Disease Consortium, whose members are from the UCL Institute of Neurology, the University of Sheffield, and the MRC Protein Phosphorylation Unit at the University of Dundee. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.</funding-statement>
</funding-group>
<counts><page-count count="8"></page-count>
</counts>
</article-meta>
</front>
<body><sec id="s1"><title>Introduction</title>
<p>Neurodegenerative diseases, including Alzheimer's disease (AD), Parkinson's disease (PD), frontotemporal dementia, amyotrophic lateral sclerosis (ALS), Huntington's disease (HD), ataxias and dystonias are a major socioeconomic problem, and understanding the biological basis of neuronal death in these disorders is a major challenge for basic research. Many of the loci responsible for early-onset, familial forms of these disorders have been identified. Mutations in <italic>APP</italic>
, <italic>PS1</italic>
and <italic>PS2</italic>
are associated with AD <xref ref-type="bibr" rid="pone.0043099-Goate1">[1]</xref>
–<xref ref-type="bibr" rid="pone.0043099-Sherrington1">[4]</xref>
, <italic>SNCA</italic>
, <italic>LRRK2</italic>
, <italic>PRKN</italic>
, <italic>PINK1</italic>
and <italic>GBA</italic>
<xref ref-type="bibr" rid="pone.0043099-Kitada1">[5]</xref>
–<xref ref-type="bibr" rid="pone.0043099-Valente1">[9]</xref>
are associated with PD; <italic>SOD1</italic>
, <italic>TARDP</italic>
and <italic>FUS</italic>
mutations lead to familial ALS <xref ref-type="bibr" rid="pone.0043099-Rosen1">[10]</xref>
–<xref ref-type="bibr" rid="pone.0043099-Vance1">[12]</xref>
; frontotemporal dementia and parkinsonism linked to chromosome-17 is associated with <italic>MAPT</italic>
(FTDP-17T) and <italic>PGRN</italic>
mutations (FTDP-17U/GRN) <xref ref-type="bibr" rid="pone.0043099-Baker1">[13]</xref>
–<xref ref-type="bibr" rid="pone.0043099-Hutton1">[15]</xref>
; and CAG expansion of the <italic>HTT</italic>
gene causes HD <xref ref-type="bibr" rid="pone.0043099-The1">[16]</xref>
.</p>
<p>Using this genetic information as a basis for developing cell and animal models has greatly enhanced our understanding of the biological mechanisms underlying neuronal degeneration in these disorders. However, current cell models of neurological disease are limited by two major drawbacks: non-physiological protein expression levels and/or a non-neuronal cell type <xref ref-type="bibr" rid="pone.0043099-Bottomley1">[17]</xref>
–<xref ref-type="bibr" rid="pone.0043099-Gibbs1">[19]</xref>
. Patient-derived cells such as fibroblasts have been used as models in several studies looking at the basis of neurological disorders, including AD <xref ref-type="bibr" rid="pone.0043099-Yu1">[20]</xref>
. Recently, human somatic cells, such as fibroblasts, were reprogrammed to pluripotency by the exogenous expression of the transcription factors OCT4, SOX2, KLF4 NANOG, LIN28 and MYC <xref ref-type="bibr" rid="pone.0043099-Yu1">[20]</xref>
–<xref ref-type="bibr" rid="pone.0043099-Park1">[22]</xref>
. These induced pluripotent stem cells (iPSC) can be subsequently differentiated into neurons and glia, therefore by generating iPSC from patients carrying disease-linked mutations physiological expression of mutated genes in the cell type specifically affected in disease can be achieved. This technology has already been used to successfully model a range of neurological diseases including AD, PD, ALS and Ataxia <xref ref-type="bibr" rid="pone.0043099-Devine1">[23]</xref>
–<xref ref-type="bibr" rid="pone.0043099-Cooper1">[27]</xref>
.</p>
<p>Despite the fact that many of these diseases are adult onset, several groups have used iPSCs to model aspects of disease pathology. Perhaps the most notable of these is AD, where cells derived from patients with mutations in several genes have successfully recapitulated common pathology. Neurons generated from patients carrying point mutations in PSEN1, APP duplications and trisomy 21 (and thus an extra copy of the APP gene) each faithfully recapitulate features of AD pathology including increased Aβ production and elevated tau phosphorylation <xref ref-type="bibr" rid="pone.0043099-Qiang1">[26]</xref>
, <xref ref-type="bibr" rid="pone.0043099-Shi1">[28]</xref>
, <xref ref-type="bibr" rid="pone.0043099-Israel1">[29]</xref>
. The presence of overlapping phenotypes in multiple patients with the same mutation, as well as mutations in different genes linked to the same disease, provides increased confidence that iPSC can be used to reveal disease phenotypes. Importantly, gamma secretase inhibitors prevented increased Aβ production in these cells, demonstrating the suitability of iPSC-neurons as a platform for drug screening <xref ref-type="bibr" rid="pone.0043099-Qiang1">[26]</xref>
, <xref ref-type="bibr" rid="pone.0043099-Israel1">[29]</xref>
.</p>
<p>Further, iPSC have provided evidence for the importance of correct cellular context in disease models. Spinocerebellar ataxia type 3 is caused by an expansion of a polyglutamine coding repeat in the <italic>ATXN3</italic>
gene. iPSC-neurons generated from SCA3 patients recapitulate the pathological hallmark of SCA3 patients: accumulation of detergent-insoluble aggregates of full length and cleaved Ataxin 3 <xref ref-type="bibr" rid="pone.0043099-Koch1">[25]</xref>
. This phenotype was specific to neurons, and furthermore was dependent on the presence of functional ion channels, demonstrating the ability of iPSC to uncover disease mechanisms by allowing the study of mutations in the context of functional human neurons.</p>
<p>The use of iPSC as disease models is reviewed comprehensively by Cherry et al <xref ref-type="bibr" rid="pone.0043099-Cherry1">[30]</xref>
. There is now compelling evidence of the power of patient-derived iPSC to model disease pathology, offer insight into disease mechanisms and act as a platform for drug screening. However, it has also become apparent that there is extensive intra- and inter- patient variability (23, 25), and it is necessary to use both multiple iPSC lines per patient and multiple patients per gene in order to reliably assign disease phenotypes.</p>
<p>Although the sporadic forms of AD, PD and ALS are common, the familial forms caused by defined mutations are relatively rare, and for many research groups interested in these and other rarer neurological diseases, the limiting factor in the use of iPSC is access to patient fibroblasts with the disease-causing mutations of interest. For HD, where all affected individuals have the same type of mutation, an expanded CAG trinucleotide repeat, it is desirable to have access to subjects with a range of expansion size, which is the primary determinant of the rate of pathogenesis. Furthermore, recent reports have demonstrated the necessity of using multiple patient lines with mutations in the same gene, in order to ensure that observed cellular phenotypes are caused by the genetic lesion of interest and not patient variability <xref ref-type="bibr" rid="pone.0043099-Koch1">[25]</xref>
, <xref ref-type="bibr" rid="pone.0043099-Qiang1">[26]</xref>
. With this in mind, our goal was to generate a resource of fibroblast cell lines with mutations that are linked to neurological disease. There are currently 67 mutation-defined fibroblast lines available to request from the Coriell repository, and more lines currently undergoing expansion and quality control. These include cell lines with multiple different mutations in each specific gene as well as cell lines from multiple patients carrying the same mutation. Further lines will be collected and deposited as patients are identified in clinics for participation in this study. This represents a significant resource that will encourage the use of patient-derived cell models in research by the wider scientific community.</p>
</sec>
<sec sec-type="methods" id="s2"><title>Methods</title>
<sec id="s2a"><title>Patient consent and protection of privacy</title>
<p>In this study, for all biopsy samples taken, the subsequent generation and distribution of human cell lines, and the deposition of these cell lines in the NINDS repository were agreed by the patients using consent forms and patient information sheets that were reviewed and approved by local research ethics committees. Each sample is pseudoanonymised in a systematic way upon leaving the clinic. There are minor physical risks associated with the skin punch biopsy procedure, including the possibility of infection. These risks, as well as the relative benefits of participating in this study are also discussed with participants during the informed consent process. It is stressed that immediate benefits to the patients themselves are unlikely, but use of these cell lines for <italic>in vitro</italic>
research will lead to an overall enhancement of our understanding of the basic disease mechanisms. In the future, this could result in the development of novel therapeutics. For some lines, consent specifically includes commercial use of the cells and pathogenic pathway discovery (but not for direct cellular therapeutics). However, cell lines will not be sold for profit and patients are informed that they will not benefit financially from any products or tests that arise from the use of these cells. We have found that patients were typically enthusiastic about participation in this study, and we are confident that we will expand our collection of patient-derived cell lines in the future.</p>
</sec>
<sec id="s2b"><title>Fibroblast generation</title>
<p>Fibroblasts were generated from a 3–6 mm skin punch biopsy taken under local anaesthetic following informed consent. Biopsies were dissected into ∼1 mm pieces and cultured in 5 cm<sup>2</sup>
petri dishes in DMEM, 10% FBS, 1% L-Glutamine until fibroblasts were seen to grow out from the explants. When fibroblasts reached confluency, they were detached from culture dishes using TrypleE (Invitrogen) and transferred to larger culture vessels for further expansion. Cells are frozen at the lowest passage possible while still obtaining an adequate number of total cells for distribution (typically 2–4 passages or approximately 2×10<sup>7</sup>
total cells; cells are distributed at 5×10<sup>5</sup>
cells per ampoule). The passage number of the cells on distribution depends on demand for a particular cell line, however 40–60 ampoules of cells are generally derived per biopsy, whilst keeping the passage number between 2–4. Cells will be distributed at the lowest available passage, which is indicated for each sample listed in the Repository online catalogue.</p>
</sec>
<sec id="s2c"><title>Quality control of fibroblast cultures</title>
<p>Fibroblast cultures are tested for Mycoplasma contamination prior to frozen storage, and after recovery from liquid nitrogen prior to distribution. The gender of cell lines is verified by PCR with a Y chromosome-specific primer pair. Replicate cultures or matched cultures of differing cell types from the same individual are analyzed by PCR using microsatellite and Y chromosome-specific primer pairs to assure cell culture identity.</p>
</sec>
<sec id="s2d"><title>Immunocytochemistry</title>
<p>Fibroblasts were fixed in 4% paraformaldehyde for 30 min at room temperature then blocked and permeabilised in blocking buffer (10% FBS, 0.1% Triton X-100 in phosphate buffered saline) for 30 min at room temperature. Cells were incubated with rabbit polyclonal anti-FSP1 (1∶100, Abcam) and mouse monoclonal anti-human fibroblasts clone TE-7 (1∶100, Millipore) diluted in blocking buffer overnight at 4°C. Cells were then incubated with Alexa Fluor 488 and 568 antibodies (1∶500) for 1 h at room temperature and nuclei were stained using DAPI. Images were acquired using a Zeiss LSM 710 confocal microscope.</p>
</sec>
<sec id="s2e"><title>Western blotting</title>
<p>Cells were washed in PBS and then lysed on ice for 30 minutes in lysis buffer (50 mM Tris-HCl, 150 mM NaCl, 1% v/v Tween-20, 0.2% NP40, 10%v/v Glycerol) containing Complete protease inhibitor cocktail (Roche). Lysates were centrifuged for 10 min at 11,000 g<sub>(av)</sub>
, 4°C and protein concentrations were estimated using the BioRad DC Protein Assay Kit. Equal amounts of protein were electrophoresed on NuPAGE 4–12% Bis-Tris Gels (Invitrogen) and transferred onto nitrocellulose membranes (Whatman). Membranes were probed with primary antibodies to FSP-1 (rabbit polyclonal, 1∶500, Abcam) and β-actin (mouse monoclonal, 1∶5000, Sigma Aldrich) overnight at 4°C. Membranes were then incubated with appropriate secondary antibodies (AlexaFluor 680 anti-mouse IgG, Invitrogen and IRDye 800 anti-rabbit IgG, Rockland Immunochemicals, both 1∶5000) for 1 h at RT before visualisation using an Odyssey Infrared imaging system (LI-COR Biosciences).</p>
</sec>
<sec id="s2f"><title>Population doubling levels</title>
<p>Population doubling level (PDL) is a measurement of the total number of times the cells within the population have doubled since their primary isolation. PDLs were calculated using the following equation:<disp-formula id="pone.0043099.e001"><graphic xlink:href="pone.0043099.e001"></graphic>
</disp-formula>
The total viable cells at seed was determined at the first seeding following proliferation of cells from the skin explant, or from the frozen ampoule for fibroblast cultures generated outside of Coriell. The total number of viable cells at harvest was determined immediately prior to cryopreservation.</p>
</sec>
</sec>
<sec id="s3"><title>Results</title>
<sec id="s3a"><title>Collection of fibroblast cell lines</title>
<p>We have generated a collection of fibroblast cell lines from patients with mutations that are linked to neurodegenerative disorders, including AD, PD, ALS, FTD, HD, dystonias and ataxias. Also included in the collection are idiopathic sporadic Parkinson's disease fibroblast lines and normal control fibroblast lines, including family members of mutation carriers. These have been deposited in the National Institute for Neurological Disorders and Stroke (NINDS) Repository at the Coriell Institute for Medical Research (Camden, NJ) and the lines carrying known mutations are detailed in <xref ref-type="table" rid="pone-0043099-t001">Table 1</xref>
. Access to these cell lines is open to the scientific community and they are available to all researchers for use in basic research. This collection will be continually expanded and will be a valuable resource for research into basic disease mechanisms of neurological disorders. An up to date list of lines available upon request from the NINDS Repository can be found at: <ext-link ext-link-type="uri" xlink:href="http://ccr.coriell.org/sections/collections/NINDS/FibroSubcollList.aspx?SsId=10&PgId=681">http://ccr.coriell.org/sections/collections/NINDS/FibroSubcollList.aspx?SsId=10&PgId=681</ext-link>
.</p>
<table-wrap id="pone-0043099-t001" orientation="portrait" position="float"><object-id pub-id-type="doi">10.1371/journal.pone.0043099.t001</object-id>
<label>Table 1</label>
<caption><title>Fibroblast lines generated in this study.</title>
</caption>
<alternatives><graphic id="pone-0043099-t001-1" xlink:href="pone.0043099.t001"></graphic>
<table frame="hsides" rules="groups"><colgroup span="1"><col align="left" span="1"></col>
<col align="center" span="1"></col>
<col align="center" span="1"></col>
<col align="center" span="1"></col>
<col align="center" span="1"></col>
<col align="center" span="1"></col>
<col align="center" span="1"></col>
</colgroup>
<thead><tr><td align="left" rowspan="1" colspan="1">Clinical</td>
<td align="left" rowspan="1" colspan="1">Gene</td>
<td align="left" rowspan="1" colspan="1">Inheritance</td>
<td align="left" rowspan="1" colspan="1">Mutation</td>
<td align="left" rowspan="1" colspan="1">Number of lines</td>
<td align="left" rowspan="1" colspan="1">Status</td>
<td align="left" rowspan="1" colspan="1">Reference</td>
</tr>
</thead>
<tbody><tr><td align="left" rowspan="1" colspan="1">AD</td>
<td align="left" rowspan="1" colspan="1"><italic>PSEN1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">Y115H</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Submitted</td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Campion1">[33]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>PSEN1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">M146I</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Jorgensen1">[34]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>PSEN1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">E184D</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Janssen1">[35]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>PSEN1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">P264L</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Campion1">[33]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>PSEN1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">R278I</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Submitted</td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Godbolt1">[36]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">PD</td>
<td align="left" rowspan="1" colspan="1"><italic>SNCA</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">Triplication</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Gwinn1">[37]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>LRRK2</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">R1441G</td>
<td align="left" rowspan="1" colspan="1">2</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>LRRK2</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">R1441C</td>
<td align="left" rowspan="1" colspan="1">2</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Wszolek1">[38]</xref>
, <xref ref-type="bibr" rid="pone.0043099-Zimprich1">[39]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>LRRK2</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">G2019S</td>
<td align="left" rowspan="1" colspan="1">20</td>
<td align="left" rowspan="1" colspan="1">19 Available</td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Healy1">[40]</xref>
–<xref ref-type="bibr" rid="pone.0043099-Alcalay1">[42]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>LRRK2</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">G2019S homozygote</td>
<td align="left" rowspan="1" colspan="1">2</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Ishihara1">[43]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>GBA</italic>
</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1">N370S</td>
<td align="left" rowspan="1" colspan="1">4</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Alcalay1">[42]</xref>
, <xref ref-type="bibr" rid="pone.0043099-Clark2">[44]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>GBA</italic>
</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1">L444P</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Alcalay1">[42]</xref>
, <xref ref-type="bibr" rid="pone.0043099-Clark2">[44]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>PARK2</italic>
</td>
<td align="left" rowspan="1" colspan="1">R</td>
<td align="left" rowspan="1" colspan="1">R42P, ΔExon 3</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Marder1">[45]</xref>
, <xref ref-type="bibr" rid="pone.0043099-Clark3">[46]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>PARK2</italic>
</td>
<td align="left" rowspan="1" colspan="1">R</td>
<td align="left" rowspan="1" colspan="1">Δ255, ΔExon 3–4</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Marder1">[45]</xref>
, <xref ref-type="bibr" rid="pone.0043099-Clark3">[46]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>PARK2</italic>
</td>
<td align="left" rowspan="1" colspan="1">R</td>
<td align="left" rowspan="1" colspan="1">ΔExon 3–4 homozygote</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Submitted</td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>PARK2</italic>
</td>
<td align="left" rowspan="1" colspan="1">R</td>
<td align="left" rowspan="1" colspan="1">R275W/R275Q</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Puschmann1">[47]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>PINK1</italic>
</td>
<td align="left" rowspan="1" colspan="1">R</td>
<td align="left" rowspan="1" colspan="1">Q456X homozygote</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>PINK1</italic>
</td>
<td align="left" rowspan="1" colspan="1">R</td>
<td align="left" rowspan="1" colspan="1">D525N/W577R</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">HD</td>
<td align="left" rowspan="1" colspan="1"><italic>HTT</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">CAG repeat, range 38–57</td>
<td align="left" rowspan="1" colspan="1">17</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">ALS</td>
<td align="left" rowspan="1" colspan="1"><italic>SOD1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">A4V</td>
<td align="left" rowspan="1" colspan="1">2</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>SOD1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">C38G</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>SOD1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">L38V</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>SOD1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">E49K</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>SOD1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">G86R</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>SOD1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">A89V</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>SOD1</italic>
</td>
<td align="left" rowspan="1" colspan="1">R</td>
<td align="left" rowspan="1" colspan="1">D90A</td>
<td align="left" rowspan="1" colspan="1">2</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>SOD1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">D91A</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>SOD1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">E100G</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>SOD1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">N138K</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>SOD1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">I112T</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>SOD1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">I113T</td>
<td align="left" rowspan="1" colspan="1">6</td>
<td align="left" rowspan="1" colspan="1">2 Available</td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>SOD1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">L144P</td>
<td align="left" rowspan="1" colspan="1">2</td>
<td align="left" rowspan="1" colspan="1">1 Available</td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>SOD1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">V148G</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>TARDBP</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">G298S</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">FTDP-17T</td>
<td align="left" rowspan="1" colspan="1"><italic>MAPT</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">P301L</td>
<td align="left" rowspan="1" colspan="1">2</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Narozanska1">[48]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>MAPT</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">V337M</td>
<td align="left" rowspan="1" colspan="1">2</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Whitwell1">[49]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>MAPT</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">N279K</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Wszolek2">[50]</xref>
, <xref ref-type="bibr" rid="pone.0043099-Tsuboi1">[51]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>MAPT</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">Exon 10+16</td>
<td align="left" rowspan="1" colspan="1">5</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Janssen2">[52]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>MAPT</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">R406W</td>
<td align="left" rowspan="1" colspan="1">2</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Kantarci1">[53]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">FTDP-17U</td>
<td align="left" rowspan="1" colspan="1"><italic>GRN</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">A9D</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Gass1">[54]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><italic>GRN</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">R493X</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Rohrer1">[55]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">FTD</td>
<td align="left" rowspan="1" colspan="1"><italic>VCP</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">R155H</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Miller1">[56]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Perry Syndrome</td>
<td align="left" rowspan="1" colspan="1"><italic>DCTN1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">T72P</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1">Available</td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-Farrer1">[57]</xref>
, <xref ref-type="bibr" rid="pone.0043099-Wider1">[58]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Dystonia</td>
<td align="left" rowspan="1" colspan="1"><italic>THAP1</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">I149T</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"><xref ref-type="bibr" rid="pone.0043099-VanGerpen1">[59]</xref>
, <xref ref-type="bibr" rid="pone.0043099-Ledoux1">[60]</xref>
</td>
</tr>
<tr><td align="left" rowspan="1" colspan="1">Ataxia</td>
<td align="left" rowspan="1" colspan="1"><italic>CACNA1A</italic>
</td>
<td align="left" rowspan="1" colspan="1">D</td>
<td align="left" rowspan="1" colspan="1">R1346X</td>
<td align="left" rowspan="1" colspan="1">1</td>
<td align="left" rowspan="1" colspan="1"></td>
<td align="left" rowspan="1" colspan="1"></td>
</tr>
</tbody>
</table>
</alternatives>
<table-wrap-foot><fn id="nt101"><label></label>
<p>Disease, gene, mutation and mode of inheritance for fibroblast cell lines. The current status of each line (available, submitted but not yet in catalogue) is indicated. Where the status is left blank, this indicates fibroblast lines have been generated but are awaiting submission to the NINDS repository. All variants are heterozygous unless otherwise stated. References indicate where families have been described in the literature. D = autosomal dominant, R = autosomal recessive.</p>
</fn>
</table-wrap-foot>
</table-wrap>
<p>Fibroblast cell lines are deposited along with a clinical data elements (CDE) form that outlines the clinical background of the patient from whom the cells are derived. This protects the identity of the patient (see below) while providing the end-user with confidence in the clinical diagnosis. CDE's for PD, ALS, and HD have been developed with input from researchers in the field. For AD and other dementia cell lines, there is currently no CDE; however, information (e.g., sex, year of birth, and MMSE score at the time of biopsy) is included.</p>
<p>Fibroblast cultures are available upon request to all research laboratories, including those in industry. Users wishing to request cells are asked to complete a statement of research intent and complete a NINDS Repository Materials Transfer Agreement (MTA).</p>
</sec>
<sec id="s3b"><title>Skin explant-derived cell lines express the fibroblast-specific proteins FSP1 and TE7</title>
<p>For all fibroblast lines generated, the identity and purity of each line was confirmed by assessment of characteristic spindle-shaped morphology (<xref ref-type="fig" rid="pone-0043099-g001">Fig. 1A</xref>
) <xref ref-type="bibr" rid="pone.0043099-Strutz1">[31]</xref>
. We also immunostained a subset of lines (n = 6) for fibroblast-specific protein 1 (FSP1) and TE-7, which detects an epitope specifically expressed by cells that are mesenchymal in origin. All fibroblast lines examined showed strong cytoplasmic staining of both FSP1 and TE7, confirming that cells cultures established from skin explants are indeed fibroblasts (<xref ref-type="fig" rid="pone-0043099-g001">Fig. 1B</xref>
). Next, we examined the expression of FSP1 and TE-7 over multiple passages, to ensure that the properties of the fibroblast lines were not altered by increased time in culture. We found that the morphology of fibroblast lines remained unchanged throughout five consecutive passages. Likewise, FSP1 and TE-7 were highly expressed in all cells and did not show altered levels, or altered distribution, during continuous culture (<xref ref-type="fig" rid="pone-0043099-g002">Fig. 2A</xref>
). FSP1 levels were also examined by western blot (<xref ref-type="fig" rid="pone-0043099-g002">Figure 2B</xref>
). In fibroblast cell lysates, FSP1 was detected as a single band at the expected molecular weight of 12 kDa (<xref ref-type="fig" rid="pone-0043099-g002">Fig. 2B</xref>
). FSP1 was expressed at high levels in all cell lines examined (n = 6) and the levels of FSP1 were not different between cell lines, or between different passages.</p>
<fig id="pone-0043099-g001" orientation="portrait" position="float"><object-id pub-id-type="doi">10.1371/journal.pone.0043099.g001</object-id>
<label>Figure 1</label>
<caption><title>Fibroblast cultures express the mesenchymal markers FSP1 and TE7.</title>
<p>Cells generated from skin punch biopsies were verified as fibroblasts by morphological assessment (A) and positive staining with antibodies to fibroblast-specific protein 1 (FSP1) and fibroblast-specific clone TE7 (B, 63×). All fibroblasts examined (n = 6) demonstrated positive staining with both antibodies.</p>
</caption>
<graphic xlink:href="pone.0043099.g001"></graphic>
</fig>
<fig id="pone-0043099-g002" orientation="portrait" position="float"><object-id pub-id-type="doi">10.1371/journal.pone.0043099.g002</object-id>
<label>Figure 2</label>
<caption><title>Fibroblast morphology and marker expression remain consistent during prolonged culture.</title>
<p>Fibroblast lines were immunostained with antibodies FSP1 and TE7 at multiple consecutive passages (A). Passage numbers are indicated above the panels. Morphology, FSP1 and TE7 staining did not change during five consecutive subculturings (n = 6, representative images from line NM34737, carrying the PSEN1 M146I mutation are shown). FSP1 levels were also detected by western blotting of fibroblast cell lysates (B). FSP1 was detected as a single band at 12 kDa in all fibroblast lines examined (top panel, n = 6). β-actin was used as a loading control (bottom panel). No variation in FSP1 levels was observed between passages or between cell lines.</p>
</caption>
<graphic xlink:href="pone.0043099.g002"></graphic>
</fig>
</sec>
<sec id="s3c"><title>Population doubling levels</title>
<p>Fibroblasts have a limited proliferative lifespan in culture, and are able to complete a finite number of cell divisions before reaching senescence (the Hayflick limit) <xref ref-type="bibr" rid="pone.0043099-Hayflick1">[61]</xref>
. As passage number is a reflection only of the number of times a particular cell line has been subcultured, and not a reflection of the absolute time in culture of that particular cell line, the population doubling level (PDL) of each fibroblast line available in the NINDS catalogue was determined. PDL is a measure of the total number of times a cell population has doubled since its initial isolation <italic>in vitro</italic>
. The PDLs of fibroblast lines in our collection varied from 2.89–7.7 (<xref ref-type="supplementary-material" rid="pone.0043099.s001">Table S1</xref>
). <xref ref-type="fig" rid="pone-0043099-g003">Fig. 3</xref>
shows the range and mean PDLs of the control fibroblasts, and fibroblast lines from each disease group. A similar range of PDL variability was seen across all disease groups and the mean PDLs of fibroblasts were ∼5 for each of the categories represented by the collection. Thus, fibroblast lines requested from the NINDS repository are comparable in terms of the absolute time in culture of the cell. Senescence of human diploid fibroblast cultures does not occur until after 40–50 population doublings <xref ref-type="bibr" rid="pone.0043099-Kitada2">[62]</xref>
. Therefore, cell cultures within our collection have low population doubling numbers and can be expanded sufficiently by the end-users prior to senescence. Furthermore, although the proliferative capacity of the starting cell population may impact on reprogramming efficiency, both our control and disease lines should retain sufficient proliferative capacity to be suitable for reprogramming to iPSCs.</p>
<fig id="pone-0043099-g003" orientation="portrait" position="float"><object-id pub-id-type="doi">10.1371/journal.pone.0043099.g003</object-id>
<label>Figure 3</label>
<caption><title>Population doubling levels of fibroblast cell lines.</title>
<p>Population doubling levels were calculated for each of the cell lines available in the NINDS repository at the time of cryopreservation. Individual points of the graph correspond to the PDL of individual fibroblast lines, the horizontal line represents the mean PDL for each disease category. PDLs ranged between 2–8 with a mean PDL of ∼5 for both control and disease cell lines. A full list of PDLs for individual cell lines in provided in <xref ref-type="supplementary-material" rid="pone.0043099.s001">Table S1</xref>
.</p>
</caption>
<graphic xlink:href="pone.0043099.g003"></graphic>
</fig>
</sec>
</sec>
<sec id="s4"><title>Discussion</title>
<p>The search for the genetic basis of disease has provided the impetus for the generation of animal and cell models that recapitulate key disease features and allow better understanding of the underlying biological mechanisms leading to cell death. A major challenge to understanding the basis of neurological disorders is our ability to model disease causing mutations at physiological levels, in a relevant cell type. The recent development of iPSCs, which can subsequently be differentiated into neurons and glial cells, is redefining the way we approach <italic>in vitro</italic>
modelling of neurological disorders. We have developed a collection of primary fibroblast lines from patients carrying mutations that are associated with neurological disorders that can be accessed by all bona fide research groups.</p>
<p>Although others have developed collections of disease-specific iPSCs <xref ref-type="bibr" rid="pone.0043099-Park2">[32]</xref>
, we focussed on developing fibroblast cell lines. The cell lines in our collection express high levels of the fibroblast markers FSP-1 and TE-7, and are cryopreserved at low population doubling levels for distribution. However, although fibroblasts are the most common cell type in cultures established from dermal outgrowths, these cultures actually represent a heterogeneous cell population including endothelial cells, pericytes and several types of stem/progenitor cells <xref ref-type="bibr" rid="pone.0043099-Kitada2">[62]</xref>
. This cellular diversity could influence the ability of each individual fibroblast line to give rise to iPSC.</p>
<p>The molecular mechanisms underlying the reprogramming of fibroblasts to iPSC are poorly understood and there has been much debate as to whether the process is stochastic (all cells within a given population have the potential to be reprogrammed) or elite (only a subset of cells with particular properties can be reprogrammed). In a recent study, Wakeo and colleagues determined that iPSC were exclusively generated from a sub-population of cells positive for both the stem cell marker SSEA3 and the mesencyhmal marker CD105 <xref ref-type="bibr" rid="pone.0043099-Wakao1">[63]</xref>
. These cells, termed muse cells (multilineage-differentiating stress enduring cells), express the pluripotency markers Oct3/4, Nanog and Sox2 and represent approximately 2% of cells present in fibroblast cultures.</p>
<p>This work provides support for the elite model of reprogramming and suggests the efficiency of reprogramming from each of the fibroblast cultures within this collection may depend on the proportion of Muse cells present, which was not examined in this study. However, even in a pure Muse cell population the efficiency of reprogramming remains low (0.03%), and it therefore seems likely that there is some stochastic influence on reprogramming. This notion is supported by multiple reports describing the addition of extra reprogramming factors and small molecules that increase the efficiency of reprogramming (reviewed in <xref ref-type="bibr" rid="pone.0043099-Feng1">[64]</xref>
). Thus, the elite vs stochastic debate remains open, but it is important for research groups requesting cells described in this manuscript to be aware of the implications of fibroblast culture diversity. By making fibroblast lines available, the end-users retain the flexibility to reprogram by their method of choice.</p>
<p>This collection contains cell lines with mutations in a wide range of genes as well as multiple different mutations in each gene. In many cases, cell lines from several patients with the same mutation are available which will control for patient variability and allow robust phenotypes to be defined. The rarity of familial forms of neurological diseases means this represents a valuable resource which we anticipate will be widely used by the scientific community, advancing the use of patient cells for <italic>in vitro</italic>
disease modelling.</p>
</sec>
<sec sec-type="supplementary-material" id="s5"><title>Supporting Information</title>
<supplementary-material content-type="local-data" id="pone.0043099.s001"><label>Table S1</label>
<caption><p><bold>Population doubling levels for fibroblast lines in the NINDS repository.</bold>
NINDS reference number, disease, mutation and population doubling level for each cell line currently available from the NINDS repository.</p>
<p>(DOCX)</p>
</caption>
<media xlink:href="pone.0043099.s001.docx" mimetype="application" mime-subtype="msword"><caption><p>Click here for additional data file.</p>
</caption>
</media>
</supplementary-material>
</sec>
</body>
<back><ack><p>We thank the patients and their families for agreeing to participate in this study. We also thank Jennifer Lash and Sharleen Traynor for study coordination for the Mayo Clinic samples, Carol Moskowitz RNC and Hele Mejia Santana for coordination of sample collection at Columbia University and Elizabeth Mossmiller for coordinating the collection of ALS samples at John Hopkins University.</p>
<p><bold>Membership of the NINDS Huntington's Disease iPSC Consortium</bold>
</p>
<p>James F. Gusella<sup>1</sup>
, Marcy E. MacDonald<sup>1</sup>
, Vanessa C. Wheeler<sup>1</sup>
, Christopher A. Ross<sup>2</sup>
, Sergey Akimov<sup>2</sup>
, Jamshid Arjomand<sup>3</sup>
, Leslie M. Thompson<sup>4</sup>
, Alvin King<sup>4</sup>
, Neal Hermanowicz<sup>4</sup>
, Sara Winokur<sup>4</sup>
, Clive N. Svendsen<sup>5</sup>
, Virginia Mattis<sup>5</sup>
, Marco Onorati<sup>6</sup>
, Elena Cattaneo<sup>6</sup>
, Nicholas D. Allen<sup>7</sup>
, Paul J. Kemp<sup>7</sup>
, Kwang-Soo Kim<sup>8</sup>
, Steven Finkbeiner<sup>9</sup>
</p>
<p>1 Center for Human Genetic Research, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, United States of America. 2 Division of Neurobiology, Department of Psychiatry, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America. 3 CHDI Foundation Inc, Princeton, New Jersey, United States of America. 4 University of California Irvine, Irvine, California, United States of America. 5 Regenerative Medicine Institute, Cedars-Sinai Medical Center, Los Angeles, California, United States of America. 6 Department of Pharmacological Sciences and Stem Cell Research, University of Milano, Italy. 7 School of Biosciences, University of Cardiff, United Kingdom. 8 McLean Hospital, Harvard Medical School, Belmont, Massachusetts, United States of America. 9 Gladstone Institute of Neurological Disease, Taube-Koret Center for Huntington's Disease Research, Departments of Neurology and Physiology, University of California San Francisco, California, Massachusetts, United States of America.</p>
<p><bold>Membership of the NINDS Parkinson's Disease iPSC Consortium</bold>
</p>
<p>Ole Isacson<sup>1</sup>
, Ted M. Dawson<sup>2</sup>
, Zbigniew K. Wszolek<sup>3</sup>
, Owen A. Ross<sup>3</sup>
, Karen S. Marder<sup>4</sup>
, Serge Przedborski<sup>4</sup>
, Jian Feng<sup>5</sup>
, Virginia M.Y. Lee<sup>6</sup>
, John Q. Trojanowski<sup>6</sup>
, D. James Surmeier<sup>7</sup>
</p>
<p>1 Center for Neuroregeneration Research, Harvard Medical School, Belmont, Massachusetts, United States of America. 2 Neuroregeneration Program, Institute of Cell Engineering, Department of Neurology and the Solomon H. Snyder Department of Neuroscience, John Hopkins University, Baltimore, Maryland, United States of America. 3 Department of Neurology, Mayo Clinic, Jacksonville, Florida, United States of America. 4 College of Physicians and Surgeons, Columbia University, New York, New York, United States of America. 5 Department of Physiology and Biophysics, State University of New York at Buffalo, Buffalo, New York, United States of America. 6 Center for Neurodegenerative Disease Research, School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America. 7 Department of Physiology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, United States of America.</p>
<p><bold>Membership of the NINDS ALS iPSC Consortium</bold>
</p>
<p>Jeffrey D. Rothstein<sup>1</sup>
, Christopher E. Henderson<sup>2</sup>
, Tom Maniatis<sup>3</sup>
, Kevin Eggan<sup>3</sup>
, Merit E. Cudowicz<sup>4</sup>
</p>
<p>1 Department of Psychiatry and Behavioural Sciences, John Hopkins University School of Medicine, Baltimore, Maryland, United States of America. 2 Motor Neuron Center, Columbia University, New York, New York, United States of America. 3 Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts, United States of America. 4 Department of Neurology, Boston Massachusetts General Hospital, Boston, Massachusetts, United States of America.</p>
</ack>
<ref-list><title>References</title>
<ref id="pone.0043099-Goate1"><label>1</label>
<mixed-citation publication-type="journal"><name><surname>Goate</surname>
<given-names>A</given-names>
</name>
, <name><surname>Chartier-Harlin</surname>
<given-names>MC</given-names>
</name>
, <name><surname>Mullan</surname>
<given-names>M</given-names>
</name>
, <name><surname>Brown</surname>
<given-names>J</given-names>
</name>
, <name><surname>Crawford</surname>
<given-names>F</given-names>
</name>
, <etal>et al</etal>
(<year>1991</year>
) <article-title>Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease</article-title>
. <source>Nature</source>
<volume>349</volume>
: <fpage>704</fpage>
–<lpage>706</lpage>
<pub-id pub-id-type="pmid">1671712</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-LevyLahad1"><label>2</label>
<mixed-citation publication-type="journal"><name><surname>Levy-Lahad</surname>
<given-names>E</given-names>
</name>
, <name><surname>Wasco</surname>
<given-names>W</given-names>
</name>
, <name><surname>Poorkaj</surname>
<given-names>P</given-names>
</name>
, <name><surname>Romano</surname>
<given-names>DM</given-names>
</name>
, <name><surname>Oshima</surname>
<given-names>J</given-names>
</name>
, <etal>et al</etal>
(<year>1995</year>
) <article-title>Candidate gene for the chromosome 1 familial Alzheimer's disease locus</article-title>
. <source>Science</source>
<volume>269</volume>
: <fpage>973</fpage>
–<lpage>977</lpage>
<pub-id pub-id-type="pmid">7638622</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Rogaev1"><label>3</label>
<mixed-citation publication-type="journal"><name><surname>Rogaev</surname>
<given-names>EI</given-names>
</name>
, <name><surname>Sherrington</surname>
<given-names>R</given-names>
</name>
, <name><surname>Rogaeva</surname>
<given-names>EA</given-names>
</name>
, <name><surname>Levesque</surname>
<given-names>G</given-names>
</name>
, <name><surname>Ikeda</surname>
<given-names>M</given-names>
</name>
, <etal>et al</etal>
(<year>1995</year>
) <article-title>Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene</article-title>
. <source>Nature</source>
<volume>376</volume>
: <fpage>775</fpage>
–<lpage>778</lpage>
<pub-id pub-id-type="pmid">7651536</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Sherrington1"><label>4</label>
<mixed-citation publication-type="journal"><name><surname>Sherrington</surname>
<given-names>R</given-names>
</name>
, <name><surname>Rogaev</surname>
<given-names>EI</given-names>
</name>
, <name><surname>Liang</surname>
<given-names>Y</given-names>
</name>
, <name><surname>Rogaeva</surname>
<given-names>EA</given-names>
</name>
, <name><surname>Levesque</surname>
<given-names>G</given-names>
</name>
, <etal>et al</etal>
(<year>1995</year>
) <article-title>Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease</article-title>
. <source>Nature</source>
<volume>375</volume>
: <fpage>754</fpage>
–<lpage>760</lpage>
<pub-id pub-id-type="pmid">7596406</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Kitada1"><label>5</label>
<mixed-citation publication-type="journal"><name><surname>Kitada</surname>
<given-names>T</given-names>
</name>
, <name><surname>Asakawa</surname>
<given-names>S</given-names>
</name>
, <name><surname>Hattori</surname>
<given-names>N</given-names>
</name>
, <name><surname>Matsumine</surname>
<given-names>H</given-names>
</name>
, <name><surname>Yamamura</surname>
<given-names>Y</given-names>
</name>
, <etal>et al</etal>
(<year>1998</year>
) <article-title>Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism</article-title>
. <source>Nature</source>
<volume>392</volume>
: <fpage>605</fpage>
–<lpage>608</lpage>
<pub-id pub-id-type="pmid">9560156</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-PaisanRuiz1"><label>6</label>
<mixed-citation publication-type="journal"><name><surname>Paisan-Ruiz</surname>
<given-names>C</given-names>
</name>
, <name><surname>Jain</surname>
<given-names>S</given-names>
</name>
, <name><surname>Evans</surname>
<given-names>EW</given-names>
</name>
, <name><surname>Gilks</surname>
<given-names>WP</given-names>
</name>
, <name><surname>Simon</surname>
<given-names>J</given-names>
</name>
, <etal>et al</etal>
(<year>2004</year>
) <article-title>Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease</article-title>
. <source>Neuron</source>
<volume>44</volume>
: <fpage>595</fpage>
–<lpage>600</lpage>
<pub-id pub-id-type="pmid">15541308</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Sidransky1"><label>7</label>
<mixed-citation publication-type="journal"><name><surname>Sidransky</surname>
<given-names>E</given-names>
</name>
, <name><surname>Nalls</surname>
<given-names>MA</given-names>
</name>
, <name><surname>Aasly</surname>
<given-names>JO</given-names>
</name>
, <name><surname>Aharon-Peretz</surname>
<given-names>J</given-names>
</name>
, <name><surname>Annesi</surname>
<given-names>G</given-names>
</name>
, <etal>et al</etal>
(<year>2009</year>
) <article-title>Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease</article-title>
. <source>N Engl J Med</source>
<volume>361</volume>
: <fpage>1651</fpage>
–<lpage>1661</lpage>
<pub-id pub-id-type="pmid">19846850</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Singleton1"><label>8</label>
<mixed-citation publication-type="journal"><name><surname>Singleton</surname>
<given-names>AB</given-names>
</name>
, <name><surname>Farrer</surname>
<given-names>M</given-names>
</name>
, <name><surname>Johnson</surname>
<given-names>J</given-names>
</name>
, <name><surname>Singleton</surname>
<given-names>A</given-names>
</name>
, <name><surname>Hague</surname>
<given-names>S</given-names>
</name>
, <etal>et al</etal>
(<year>2003</year>
) <article-title>alpha-Synuclein locus triplication causes Parkinson's disease</article-title>
. <source>Science</source>
<volume>302</volume>
: <fpage>841</fpage>
<pub-id pub-id-type="pmid">14593171</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Valente1"><label>9</label>
<mixed-citation publication-type="journal"><name><surname>Valente</surname>
<given-names>EM</given-names>
</name>
, <name><surname>Abou-Sleiman</surname>
<given-names>PM</given-names>
</name>
, <name><surname>Caputo</surname>
<given-names>V</given-names>
</name>
, <name><surname>Muqit</surname>
<given-names>MM</given-names>
</name>
, <name><surname>Harvey</surname>
<given-names>K</given-names>
</name>
, <etal>et al</etal>
(<year>2004</year>
) <article-title>Hereditary early-onset Parkinson's disease caused by mutations in PINK1</article-title>
. <source>Science</source>
<volume>304</volume>
: <fpage>1158</fpage>
–<lpage>1160</lpage>
<pub-id pub-id-type="pmid">15087508</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Rosen1"><label>10</label>
<mixed-citation publication-type="journal"><name><surname>Rosen</surname>
<given-names>DR</given-names>
</name>
, <name><surname>Siddique</surname>
<given-names>T</given-names>
</name>
, <name><surname>Patterson</surname>
<given-names>D</given-names>
</name>
, <name><surname>Figlewicz</surname>
<given-names>DA</given-names>
</name>
, <name><surname>Sapp</surname>
<given-names>P</given-names>
</name>
, <etal>et al</etal>
(<year>1993</year>
) <article-title>Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis</article-title>
. <source>Nature</source>
<volume>362</volume>
: <fpage>59</fpage>
–<lpage>62</lpage>
<pub-id pub-id-type="pmid">8446170</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Sreedharan1"><label>11</label>
<mixed-citation publication-type="journal"><name><surname>Sreedharan</surname>
<given-names>J</given-names>
</name>
, <name><surname>Blair</surname>
<given-names>IP</given-names>
</name>
, <name><surname>Tripathi</surname>
<given-names>VB</given-names>
</name>
, <name><surname>Hu</surname>
<given-names>X</given-names>
</name>
, <name><surname>Vance</surname>
<given-names>C</given-names>
</name>
, <etal>et al</etal>
(<year>2008</year>
) <article-title>TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis</article-title>
. <source>Science</source>
<volume>319</volume>
: <fpage>1668</fpage>
–<lpage>1672</lpage>
<pub-id pub-id-type="pmid">18309045</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Vance1"><label>12</label>
<mixed-citation publication-type="journal"><name><surname>Vance</surname>
<given-names>C</given-names>
</name>
, <name><surname>Rogelj</surname>
<given-names>B</given-names>
</name>
, <name><surname>Hortobagyi</surname>
<given-names>T</given-names>
</name>
, <name><surname>De Vos</surname>
<given-names>KJ</given-names>
</name>
, <name><surname>Nishimura</surname>
<given-names>AL</given-names>
</name>
, <etal>et al</etal>
(<year>2009</year>
) <article-title>Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6</article-title>
. <source>Science</source>
<volume>323</volume>
: <fpage>1208</fpage>
–<lpage>1211</lpage>
<pub-id pub-id-type="pmid">19251628</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Baker1"><label>13</label>
<mixed-citation publication-type="journal"><name><surname>Baker</surname>
<given-names>M</given-names>
</name>
, <name><surname>Mackenzie</surname>
<given-names>IR</given-names>
</name>
, <name><surname>Pickering-Brown</surname>
<given-names>SM</given-names>
</name>
, <name><surname>Gass</surname>
<given-names>J</given-names>
</name>
, <name><surname>Rademakers</surname>
<given-names>R</given-names>
</name>
, <etal>et al</etal>
(<year>2006</year>
) <article-title>Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17</article-title>
. <source>Nature</source>
<volume>442</volume>
: <fpage>916</fpage>
–<lpage>919</lpage>
<pub-id pub-id-type="pmid">16862116</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Cruts1"><label>14</label>
<mixed-citation publication-type="journal"><name><surname>Cruts</surname>
<given-names>M</given-names>
</name>
, <name><surname>Gijselinck</surname>
<given-names>I</given-names>
</name>
, <name><surname>van der Zee</surname>
<given-names>J</given-names>
</name>
, <name><surname>Engelborghs</surname>
<given-names>S</given-names>
</name>
, <name><surname>Wils</surname>
<given-names>H</given-names>
</name>
, <etal>et al</etal>
(<year>2006</year>
) <article-title>Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21</article-title>
. <source>Nature</source>
<volume>442</volume>
: <fpage>920</fpage>
–<lpage>924</lpage>
<pub-id pub-id-type="pmid">16862115</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Hutton1"><label>15</label>
<mixed-citation publication-type="journal"><name><surname>Hutton</surname>
<given-names>M</given-names>
</name>
, <name><surname>Lendon</surname>
<given-names>CL</given-names>
</name>
, <name><surname>Rizzu</surname>
<given-names>P</given-names>
</name>
, <name><surname>Baker</surname>
<given-names>M</given-names>
</name>
, <name><surname>Froelich</surname>
<given-names>S</given-names>
</name>
, <etal>et al</etal>
(<year>1998</year>
) <article-title>Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17</article-title>
. <source>Nature</source>
<volume>393</volume>
: <fpage>702</fpage>
–<lpage>705</lpage>
<pub-id pub-id-type="pmid">9641683</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-The1"><label>16</label>
<mixed-citation publication-type="journal"><collab>The Huntington's Disease Collaborative Research Group</collab>
(<year>1993</year>
) <article-title>A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group</article-title>
. <source>Cell</source>
<volume>72</volume>
: <fpage>971</fpage>
–<lpage>983</lpage>
<pub-id pub-id-type="pmid">8458085</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Bottomley1"><label>17</label>
<mixed-citation publication-type="journal"><name><surname>Bottomley</surname>
<given-names>RH</given-names>
</name>
, <name><surname>Trainer</surname>
<given-names>AL</given-names>
</name>
, <name><surname>Griffin</surname>
<given-names>MJ</given-names>
</name>
(<year>1969</year>
) <article-title>Enzymatic and chromosomal characterization of HeLa variants</article-title>
. <source>J Cell Biol</source>
<volume>41</volume>
: <fpage>806</fpage>
–<lpage>815</lpage>
<pub-id pub-id-type="pmid">5768876</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Falkenburger1"><label>18</label>
<mixed-citation publication-type="journal"><name><surname>Falkenburger</surname>
<given-names>BH</given-names>
</name>
, <name><surname>Schulz</surname>
<given-names>JB</given-names>
</name>
(<year>2006</year>
) <article-title>Limitations of cellular models in Parkinson's disease research</article-title>
. <source>J Neural Transm Suppl</source>
<fpage>261</fpage>
–<lpage>268</lpage>
<pub-id pub-id-type="pmid">17017539</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Gibbs1"><label>19</label>
<mixed-citation publication-type="journal"><name><surname>Gibbs</surname>
<given-names>JR</given-names>
</name>
, <name><surname>Singleton</surname>
<given-names>A</given-names>
</name>
(<year>2006</year>
) <article-title>Application of genome-wide single nucleotide polymorphism typing: simple association and beyond</article-title>
. <source>PLoS Genet</source>
<volume>2</volume>
: <fpage>150</fpage>
</mixed-citation>
</ref>
<ref id="pone.0043099-Yu1"><label>20</label>
<mixed-citation publication-type="journal"><name><surname>Yu</surname>
<given-names>J</given-names>
</name>
, <name><surname>Vodyanik</surname>
<given-names>MA</given-names>
</name>
, <name><surname>Smuga-Otto</surname>
<given-names>K</given-names>
</name>
, <name><surname>Antosiewicz-Bourget</surname>
<given-names>J</given-names>
</name>
, <name><surname>Frane</surname>
<given-names>JL</given-names>
</name>
, <etal>et al</etal>
(<year>2007</year>
) <article-title>Induced pluripotent stem cell lines derived from human somatic cells</article-title>
. <source>Science</source>
<volume>318</volume>
: <fpage>1917</fpage>
–<lpage>1920</lpage>
<pub-id pub-id-type="pmid">18029452</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Takahashi1"><label>21</label>
<mixed-citation publication-type="journal"><name><surname>Takahashi</surname>
<given-names>K</given-names>
</name>
, <name><surname>Tanabe</surname>
<given-names>K</given-names>
</name>
, <name><surname>Ohnuki</surname>
<given-names>M</given-names>
</name>
, <name><surname>Narita</surname>
<given-names>M</given-names>
</name>
, <name><surname>Ichisaka</surname>
<given-names>T</given-names>
</name>
, <etal>et al</etal>
(<year>2007</year>
) <article-title>Induction of pluripotent stem cells from adult human fibroblasts by defined factors</article-title>
. <source>Cell</source>
<volume>131</volume>
: <fpage>861</fpage>
–<lpage>872</lpage>
<pub-id pub-id-type="pmid">18035408</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Park1"><label>22</label>
<mixed-citation publication-type="journal"><name><surname>Park</surname>
<given-names>IH</given-names>
</name>
, <name><surname>Zhao</surname>
<given-names>R</given-names>
</name>
, <name><surname>West</surname>
<given-names>JA</given-names>
</name>
, <name><surname>Yabuuchi</surname>
<given-names>A</given-names>
</name>
, <name><surname>Huo</surname>
<given-names>H</given-names>
</name>
, <etal>et al</etal>
(<year>2008</year>
) <article-title>Reprogramming of human somatic cells to pluripotency with defined factors</article-title>
. <source>Nature</source>
<volume>451</volume>
: <fpage>141</fpage>
–<lpage>146</lpage>
<pub-id pub-id-type="pmid">18157115</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Devine1"><label>23</label>
<mixed-citation publication-type="journal"><name><surname>Devine</surname>
<given-names>MJ</given-names>
</name>
, <name><surname>Ryten</surname>
<given-names>M</given-names>
</name>
, <name><surname>Vodicka</surname>
<given-names>P</given-names>
</name>
, <name><surname>Thomson</surname>
<given-names>AJ</given-names>
</name>
, <name><surname>Burdon</surname>
<given-names>T</given-names>
</name>
, <etal>et al</etal>
(<year>2011</year>
) <article-title>Parkinson's disease induced pluripotent stem cells with triplication of the alpha-synuclein locus</article-title>
. <source>Nat Commun</source>
<volume>2</volume>
: <fpage>440</fpage>
<pub-id pub-id-type="pmid">21863007</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Dimos1"><label>24</label>
<mixed-citation publication-type="journal"><name><surname>Dimos</surname>
<given-names>JT</given-names>
</name>
, <name><surname>Rodolfa</surname>
<given-names>KT</given-names>
</name>
, <name><surname>Niakan</surname>
<given-names>KK</given-names>
</name>
, <name><surname>Weisenthal</surname>
<given-names>LM</given-names>
</name>
, <name><surname>Mitsumoto</surname>
<given-names>H</given-names>
</name>
, <etal>et al</etal>
(<year>2008</year>
) <article-title>Induced pluripotent stem cells generated from patients with ALS can be differentiated into motor neurons</article-title>
. <source>Science</source>
<volume>321</volume>
: <fpage>1218</fpage>
–<lpage>1221</lpage>
<pub-id pub-id-type="pmid">18669821</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Koch1"><label>25</label>
<mixed-citation publication-type="journal"><name><surname>Koch</surname>
<given-names>P</given-names>
</name>
, <name><surname>Breuer</surname>
<given-names>P</given-names>
</name>
, <name><surname>Peitz</surname>
<given-names>M</given-names>
</name>
, <name><surname>Jungverdorben</surname>
<given-names>J</given-names>
</name>
, <name><surname>Kesavan</surname>
<given-names>J</given-names>
</name>
, <etal>et al</etal>
(<year>2011</year>
) <article-title>Excitation-induced ataxin-3 aggregation in neurons from patients with Machado-Joseph disease</article-title>
. <source>Nature</source>
<volume>480</volume>
: <fpage>543</fpage>
–<lpage>546</lpage>
<pub-id pub-id-type="pmid">22113611</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Qiang1"><label>26</label>
<mixed-citation publication-type="journal"><name><surname>Qiang</surname>
<given-names>L</given-names>
</name>
, <name><surname>Fujita</surname>
<given-names>R</given-names>
</name>
, <name><surname>Yamashita</surname>
<given-names>T</given-names>
</name>
, <name><surname>Angulo</surname>
<given-names>S</given-names>
</name>
, <name><surname>Rhinn</surname>
<given-names>H</given-names>
</name>
, <etal>et al</etal>
(<year>2011</year>
) <article-title>Directed conversion of Alzheimer's disease patient skin fibroblasts into functional neurons</article-title>
. <source>Cell</source>
<volume>146</volume>
: <fpage>359</fpage>
–<lpage>371</lpage>
<pub-id pub-id-type="pmid">21816272</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Cooper1"><label>27</label>
<mixed-citation publication-type="journal"><name><surname>Cooper</surname>
<given-names>O</given-names>
</name>
, <name><surname>Seo</surname>
<given-names>H</given-names>
</name>
, <name><surname>Andrabi</surname>
<given-names>S</given-names>
</name>
, <name><surname>Guardia-Laguarta</surname>
<given-names>C</given-names>
</name>
, <name><surname>Graziotto</surname>
<given-names>J</given-names>
</name>
, <etal>et al</etal>
(<year>2012</year>
) <article-title>Pharmacological Rescue of Mitochondrial Deficits in iPSC-Derived Neural Cells from Patients with Familial Parkinson's Disease</article-title>
. <source>Sci Transl Med</source>
<volume>4</volume>
: <fpage>141</fpage>
</mixed-citation>
</ref>
<ref id="pone.0043099-Shi1"><label>28</label>
<mixed-citation publication-type="journal"><name><surname>Shi</surname>
<given-names>Y</given-names>
</name>
, <name><surname>Kirwan</surname>
<given-names>P</given-names>
</name>
, <name><surname>Smith</surname>
<given-names>J</given-names>
</name>
, <name><surname>Maclean</surname>
<given-names>G</given-names>
</name>
, <name><surname>Orkin</surname>
<given-names>SH</given-names>
</name>
, <etal>et al</etal>
(<year>2012</year>
) <article-title>A human stem cell model of early Alzheimer's disease pathology in down syndrome</article-title>
. <source>Sci Transl Med</source>
<volume>4</volume>
: <fpage>124ra29</fpage>
</mixed-citation>
</ref>
<ref id="pone.0043099-Israel1"><label>29</label>
<mixed-citation publication-type="journal"><name><surname>Israel</surname>
<given-names>MA</given-names>
</name>
, <name><surname>Yuan</surname>
<given-names>SH</given-names>
</name>
, <name><surname>Bardy</surname>
<given-names>C</given-names>
</name>
, <name><surname>Reyna</surname>
<given-names>SM</given-names>
</name>
, <name><surname>Mu</surname>
<given-names>Y</given-names>
</name>
, <etal>et al</etal>
(<year>2012</year>
) <article-title>Probing sporadic and familial Alzheimer's disease using induced pluripotent stem cells</article-title>
. <source>Nature</source>
<volume>482</volume>
: <fpage>216</fpage>
–<lpage>220</lpage>
<pub-id pub-id-type="pmid">22278060</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Cherry1"><label>30</label>
<mixed-citation publication-type="journal"><name><surname>Cherry</surname>
<given-names>AB</given-names>
</name>
, <name><surname>Daley</surname>
<given-names>GQ</given-names>
</name>
(<year>2012</year>
) <article-title>Reprogramming Cellular Identity for Regenerative Medicine</article-title>
. <source>Cell</source>
<volume>148</volume>
: <fpage>1110</fpage>
–<lpage>1122</lpage>
<pub-id pub-id-type="pmid">22424223</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Strutz1"><label>31</label>
<mixed-citation publication-type="journal"><name><surname>Strutz</surname>
<given-names>F</given-names>
</name>
, <name><surname>Okada</surname>
<given-names>H</given-names>
</name>
, <name><surname>Lo</surname>
<given-names>CW</given-names>
</name>
, <name><surname>Danoff</surname>
<given-names>T</given-names>
</name>
, <name><surname>Carone</surname>
<given-names>RL</given-names>
</name>
, <etal>et al</etal>
(<year>1995</year>
) <article-title>Identification and characterization of a fibroblast marker: FSP1</article-title>
. <source>J Cell Biol</source>
<volume>130</volume>
: <fpage>393</fpage>
–<lpage>405</lpage>
<pub-id pub-id-type="pmid">7615639</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Park2"><label>32</label>
<mixed-citation publication-type="journal"><name><surname>Park</surname>
<given-names>IH</given-names>
</name>
, <name><surname>Arora</surname>
<given-names>N</given-names>
</name>
, <name><surname>Huo</surname>
<given-names>H</given-names>
</name>
, <name><surname>Maherali</surname>
<given-names>N</given-names>
</name>
, <name><surname>Ahfeldt</surname>
<given-names>T</given-names>
</name>
, <etal>et al</etal>
(<year>2008</year>
) <article-title>Disease-specific induced pluripotent stem cells</article-title>
. <source>Cell</source>
<volume>134</volume>
: <fpage>877</fpage>
–<lpage>886</lpage>
<pub-id pub-id-type="pmid">18691744</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Campion1"><label>33</label>
<mixed-citation publication-type="journal"><name><surname>Campion</surname>
<given-names>D</given-names>
</name>
, <name><surname>Flaman</surname>
<given-names>JM</given-names>
</name>
, <name><surname>Brice</surname>
<given-names>A</given-names>
</name>
, <name><surname>Hannequin</surname>
<given-names>D</given-names>
</name>
, <name><surname>Dubois</surname>
<given-names>B</given-names>
</name>
, <etal>et al</etal>
(<year>1995</year>
) <article-title>Mutations of the presenilin I gene in families with early-onset Alzheimer's disease</article-title>
. <source>Hum Mol Genet</source>
<volume>4</volume>
: <fpage>2373</fpage>
–<lpage>2377</lpage>
<pub-id pub-id-type="pmid">8634712</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Jorgensen1"><label>34</label>
<mixed-citation publication-type="journal"><name><surname>Jorgensen</surname>
<given-names>P</given-names>
</name>
, <name><surname>Bus</surname>
<given-names>C</given-names>
</name>
, <name><surname>Pallisgaard</surname>
<given-names>N</given-names>
</name>
, <name><surname>Bryder</surname>
<given-names>M</given-names>
</name>
, <name><surname>Jorgensen</surname>
<given-names>AL</given-names>
</name>
(<year>1996</year>
) <article-title>Familial Alzheimer's disease co-segregates with a Met146I1e substitution in presenilin-1</article-title>
. <source>Clin Genet</source>
<volume>50</volume>
: <fpage>281</fpage>
–<lpage>286</lpage>
<pub-id pub-id-type="pmid">9007311</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Janssen1"><label>35</label>
<mixed-citation publication-type="journal"><name><surname>Janssen</surname>
<given-names>JC</given-names>
</name>
, <name><surname>Beck</surname>
<given-names>JA</given-names>
</name>
, <name><surname>Campbell</surname>
<given-names>TA</given-names>
</name>
, <name><surname>Dickinson</surname>
<given-names>A</given-names>
</name>
, <name><surname>Fox</surname>
<given-names>NC</given-names>
</name>
, <etal>et al</etal>
(<year>2003</year>
) <article-title>Early onset familial Alzheimer's disease: Mutation frequency in 31 families</article-title>
. <source>Neurology</source>
<volume>60</volume>
: <fpage>235</fpage>
–<lpage>239</lpage>
<pub-id pub-id-type="pmid">12552037</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Godbolt1"><label>36</label>
<mixed-citation publication-type="journal"><name><surname>Godbolt</surname>
<given-names>AK</given-names>
</name>
, <name><surname>Beck</surname>
<given-names>JA</given-names>
</name>
, <name><surname>Collinge</surname>
<given-names>J</given-names>
</name>
, <name><surname>Garrard</surname>
<given-names>P</given-names>
</name>
, <name><surname>Warren</surname>
<given-names>JD</given-names>
</name>
, <etal>et al</etal>
(<year>2004</year>
) <article-title>A presenilin 1 R278I mutation presenting with language impairment</article-title>
. <source>Neurology</source>
<volume>63</volume>
: <fpage>1702</fpage>
–<lpage>1704</lpage>
<pub-id pub-id-type="pmid">15534260</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Gwinn1"><label>37</label>
<mixed-citation publication-type="journal"><name><surname>Gwinn</surname>
<given-names>K</given-names>
</name>
, <name><surname>Devine</surname>
<given-names>MJ</given-names>
</name>
, <name><surname>Jin</surname>
<given-names>LW</given-names>
</name>
, <name><surname>Johnson</surname>
<given-names>J</given-names>
</name>
, <name><surname>Bird</surname>
<given-names>T</given-names>
</name>
, <etal>et al</etal>
(<year>2011</year>
) <article-title>Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by alpha-synuclein triplication (Iowa kindred)</article-title>
. <source>Mov Disord</source>
<volume>26</volume>
: <fpage>2134</fpage>
–<lpage>2136</lpage>
<pub-id pub-id-type="pmid">21656851</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Wszolek1"><label>38</label>
<mixed-citation publication-type="journal"><name><surname>Wszolek</surname>
<given-names>ZK</given-names>
</name>
, <name><surname>Pfeiffer</surname>
<given-names>B</given-names>
</name>
, <name><surname>Fulgham</surname>
<given-names>JR</given-names>
</name>
, <name><surname>Parisi</surname>
<given-names>JE</given-names>
</name>
, <name><surname>Thompson</surname>
<given-names>BM</given-names>
</name>
, <etal>et al</etal>
(<year>1995</year>
) <article-title>Western Nebraska family (family D) with autosomal dominant parkinsonism</article-title>
. <source>Neurology</source>
<volume>45</volume>
: <fpage>502</fpage>
–<lpage>505</lpage>
<pub-id pub-id-type="pmid">7898705</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Zimprich1"><label>39</label>
<mixed-citation publication-type="journal"><name><surname>Zimprich</surname>
<given-names>A</given-names>
</name>
, <name><surname>Biskup</surname>
<given-names>S</given-names>
</name>
, <name><surname>Leitner</surname>
<given-names>P</given-names>
</name>
, <name><surname>Lichtner</surname>
<given-names>P</given-names>
</name>
, <name><surname>Farrer</surname>
<given-names>M</given-names>
</name>
, <etal>et al</etal>
(<year>2004</year>
) <article-title>Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology</article-title>
. <source>Neuron</source>
<volume>44</volume>
: <fpage>601</fpage>
–<lpage>607</lpage>
<pub-id pub-id-type="pmid">15541309</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Healy1"><label>40</label>
<mixed-citation publication-type="journal"><name><surname>Healy</surname>
<given-names>DG</given-names>
</name>
, <name><surname>Falchi</surname>
<given-names>M</given-names>
</name>
, <name><surname>O'Sullivan</surname>
<given-names>SS</given-names>
</name>
, <name><surname>Bonifati</surname>
<given-names>V</given-names>
</name>
, <name><surname>Durr</surname>
<given-names>A</given-names>
</name>
, <etal>et al</etal>
(<year>2008</year>
) <article-title>Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study</article-title>
. <source>Lancet Neurol</source>
<volume>7</volume>
: <fpage>583</fpage>
–<lpage>590</lpage>
<pub-id pub-id-type="pmid">18539534</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Clark1"><label>41</label>
<mixed-citation publication-type="journal"><name><surname>Clark</surname>
<given-names>LN</given-names>
</name>
, <name><surname>Wang</surname>
<given-names>Y</given-names>
</name>
, <name><surname>Karlins</surname>
<given-names>E</given-names>
</name>
, <name><surname>Saito</surname>
<given-names>L</given-names>
</name>
, <name><surname>Mejia-Santana</surname>
<given-names>H</given-names>
</name>
, <etal>et al</etal>
(<year>2006</year>
) <article-title>Frequency of LRRK2 mutations in early- and late-onset Parkinson disease</article-title>
. <source>Neurology</source>
<volume>67</volume>
: <fpage>1786</fpage>
–<lpage>1791</lpage>
<pub-id pub-id-type="pmid">17050822</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Alcalay1"><label>42</label>
<mixed-citation publication-type="journal"><name><surname>Alcalay</surname>
<given-names>RN</given-names>
</name>
, <name><surname>Caccappolo</surname>
<given-names>E</given-names>
</name>
, <name><surname>Mejia-Santana</surname>
<given-names>H</given-names>
</name>
, <name><surname>Tang</surname>
<given-names>MX</given-names>
</name>
, <name><surname>Rosado</surname>
<given-names>L</given-names>
</name>
, <etal>et al</etal>
(<year>2010</year>
) <article-title>Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease study</article-title>
. <source>Arch Neurol</source>
<volume>67</volume>
: <fpage>1116</fpage>
–<lpage>1122</lpage>
<pub-id pub-id-type="pmid">20837857</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Ishihara1"><label>43</label>
<mixed-citation publication-type="journal"><name><surname>Ishihara</surname>
<given-names>L</given-names>
</name>
, <name><surname>Warren</surname>
<given-names>L</given-names>
</name>
, <name><surname>Gibson</surname>
<given-names>R</given-names>
</name>
, <name><surname>Amouri</surname>
<given-names>R</given-names>
</name>
, <name><surname>Lesage</surname>
<given-names>S</given-names>
</name>
, <etal>et al</etal>
(<year>2006</year>
) <article-title>Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations</article-title>
. <source>Arch Neurol</source>
<volume>63</volume>
: <fpage>1250</fpage>
–<lpage>1254</lpage>
<pub-id pub-id-type="pmid">16966502</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Clark2"><label>44</label>
<mixed-citation publication-type="journal"><name><surname>Clark</surname>
<given-names>LN</given-names>
</name>
, <name><surname>Ross</surname>
<given-names>BM</given-names>
</name>
, <name><surname>Wang</surname>
<given-names>Y</given-names>
</name>
, <name><surname>Mejia-Santana</surname>
<given-names>H</given-names>
</name>
, <name><surname>Harris</surname>
<given-names>J</given-names>
</name>
, <etal>et al</etal>
(<year>2007</year>
) <article-title>Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease</article-title>
. <source>Neurology</source>
<volume>69</volume>
: <fpage>1270</fpage>
–<lpage>1277</lpage>
<pub-id pub-id-type="pmid">17875915</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Marder1"><label>45</label>
<mixed-citation publication-type="journal"><name><surname>Marder</surname>
<given-names>KS</given-names>
</name>
, <name><surname>Tang</surname>
<given-names>MX</given-names>
</name>
, <name><surname>Mejia-Santana</surname>
<given-names>H</given-names>
</name>
, <name><surname>Rosado</surname>
<given-names>L</given-names>
</name>
, <name><surname>Louis</surname>
<given-names>ED</given-names>
</name>
, <etal>et al</etal>
(<year>2010</year>
) <article-title>Predictors of parkin mutations in early-onset Parkinson disease: the consortium on risk for early-onset Parkinson disease study</article-title>
. <source>Arch Neurol</source>
<volume>67</volume>
: <fpage>731</fpage>
–<lpage>738</lpage>
<pub-id pub-id-type="pmid">20558392</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Clark3"><label>46</label>
<mixed-citation publication-type="journal"><name><surname>Clark</surname>
<given-names>LN</given-names>
</name>
, <name><surname>Haamer</surname>
<given-names>E</given-names>
</name>
, <name><surname>Mejia-Santana</surname>
<given-names>H</given-names>
</name>
, <name><surname>Harris</surname>
<given-names>J</given-names>
</name>
, <name><surname>Lesage</surname>
<given-names>S</given-names>
</name>
, <etal>et al</etal>
(<year>2007</year>
) <article-title>Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene</article-title>
. <source>Mov Disord</source>
<volume>22</volume>
: <fpage>932</fpage>
–<lpage>937</lpage>
<pub-id pub-id-type="pmid">17415800</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Puschmann1"><label>47</label>
<mixed-citation publication-type="journal"><name><surname>Puschmann</surname>
<given-names>A</given-names>
</name>
(<year>2011</year>
) <article-title>Heredity in Parkinson's disease. From rare mutations to common genetic risk factors</article-title>
. <source>Lund University, Faculty of Medicine Doctoral Dissertation Series</source>
<volume>2011</volume>
: <fpage>95. 1</fpage>
–<lpage>174</lpage>
</mixed-citation>
</ref>
<ref id="pone.0043099-Narozanska1"><label>48</label>
<mixed-citation publication-type="journal"><name><surname>Narozanska</surname>
<given-names>E</given-names>
</name>
, <name><surname>Jasinska-Myga</surname>
<given-names>B</given-names>
</name>
, <name><surname>Sitek</surname>
<given-names>EJ</given-names>
</name>
, <name><surname>Robowski</surname>
<given-names>P</given-names>
</name>
, <name><surname>Brockhuis</surname>
<given-names>B</given-names>
</name>
, <etal>et al</etal>
(<year>2011</year>
) <article-title>Frontotemporal dementia and parkinsonism linked to chromosome 17–the first Polish family</article-title>
. <source>Eur J Neurol</source>
<volume>18</volume>
: <fpage>535</fpage>
–<lpage>537</lpage>
<pub-id pub-id-type="pmid">20561037</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Whitwell1"><label>49</label>
<mixed-citation publication-type="journal"><name><surname>Whitwell</surname>
<given-names>JL</given-names>
</name>
, <name><surname>Jack</surname>
<given-names>CR</given-names>
<suffix>Jr</suffix>
</name>
, <name><surname>Boeve</surname>
<given-names>BF</given-names>
</name>
, <name><surname>Senjem</surname>
<given-names>ML</given-names>
</name>
, <name><surname>Baker</surname>
<given-names>M</given-names>
</name>
, <etal>et al</etal>
(<year>2009</year>
) <article-title>Atrophy patterns in IVS10+16, IVS10+3, N279K, S305N, P301L, and V337M MAPT mutations</article-title>
. <source>Neurology</source>
<volume>73</volume>
: <fpage>1058</fpage>
–<lpage>1065</lpage>
<pub-id pub-id-type="pmid">19786698</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Wszolek2"><label>50</label>
<mixed-citation publication-type="journal"><name><surname>Wszolek</surname>
<given-names>ZK</given-names>
</name>
, <name><surname>Pfeiffer</surname>
<given-names>RF</given-names>
</name>
, <name><surname>Bhatt</surname>
<given-names>MH</given-names>
</name>
, <name><surname>Schelper</surname>
<given-names>RL</given-names>
</name>
, <name><surname>Cordes</surname>
<given-names>M</given-names>
</name>
, <etal>et al</etal>
(<year>1992</year>
) <article-title>Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration</article-title>
. <source>Ann Neurol</source>
<volume>32</volume>
: <fpage>312</fpage>
–<lpage>320</lpage>
<pub-id pub-id-type="pmid">1416801</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Tsuboi1"><label>51</label>
<mixed-citation publication-type="journal"><name><surname>Tsuboi</surname>
<given-names>Y</given-names>
</name>
, <name><surname>Baker</surname>
<given-names>M</given-names>
</name>
, <name><surname>Hutton</surname>
<given-names>ML</given-names>
</name>
, <name><surname>Uitti</surname>
<given-names>RJ</given-names>
</name>
, <name><surname>Rascol</surname>
<given-names>O</given-names>
</name>
, <etal>et al</etal>
(<year>2002</year>
) <article-title>Clinical and genetic studies of families with the tau N279K mutation (FTDP-17)</article-title>
. <source>Neurology</source>
<volume>59</volume>
: <fpage>1791</fpage>
–<lpage>1793</lpage>
<pub-id pub-id-type="pmid">12473774</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Janssen2"><label>52</label>
<mixed-citation publication-type="journal"><name><surname>Janssen</surname>
<given-names>JC</given-names>
</name>
, <name><surname>Warrington</surname>
<given-names>EK</given-names>
</name>
, <name><surname>Morris</surname>
<given-names>HR</given-names>
</name>
, <name><surname>Lantos</surname>
<given-names>P</given-names>
</name>
, <name><surname>Brown</surname>
<given-names>J</given-names>
</name>
, <etal>et al</etal>
(<year>2002</year>
) <article-title>Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation</article-title>
. <source>Neurology</source>
<volume>58</volume>
: <fpage>1161</fpage>
–<lpage>1168</lpage>
<pub-id pub-id-type="pmid">11971081</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Kantarci1"><label>53</label>
<mixed-citation publication-type="journal"><name><surname>Kantarci</surname>
<given-names>K</given-names>
</name>
, <name><surname>Boeve</surname>
<given-names>BF</given-names>
</name>
, <name><surname>Wszolek</surname>
<given-names>ZK</given-names>
</name>
, <name><surname>Rademakers</surname>
<given-names>R</given-names>
</name>
, <name><surname>Whitwell</surname>
<given-names>JL</given-names>
</name>
, <etal>et al</etal>
(<year>2010</year>
) <article-title>MRS in presymptomatic MAPT mutation carriers: a potential biomarker for tau-mediated pathology</article-title>
. <source>Neurology</source>
<volume>75</volume>
: <fpage>771</fpage>
–<lpage>778</lpage>
<pub-id pub-id-type="pmid">20805522</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Gass1"><label>54</label>
<mixed-citation publication-type="journal"><name><surname>Gass</surname>
<given-names>J</given-names>
</name>
, <name><surname>Cannon</surname>
<given-names>A</given-names>
</name>
, <name><surname>Mackenzie</surname>
<given-names>IR</given-names>
</name>
, <name><surname>Boeve</surname>
<given-names>B</given-names>
</name>
, <name><surname>Baker</surname>
<given-names>M</given-names>
</name>
, <etal>et al</etal>
(<year>2006</year>
) <article-title>Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration</article-title>
. <source>Hum Mol Genet</source>
<volume>15</volume>
: <fpage>2988</fpage>
–<lpage>3001</lpage>
<pub-id pub-id-type="pmid">16950801</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Rohrer1"><label>55</label>
<mixed-citation publication-type="journal"><name><surname>Rohrer</surname>
<given-names>JD</given-names>
</name>
, <name><surname>Guerreiro</surname>
<given-names>R</given-names>
</name>
, <name><surname>Vandrovcova</surname>
<given-names>J</given-names>
</name>
, <name><surname>Uphill</surname>
<given-names>J</given-names>
</name>
, <name><surname>Reiman</surname>
<given-names>D</given-names>
</name>
, <etal>et al</etal>
(<year>2009</year>
) <article-title>The heritability and genetics of frontotemporal lobar degeneration</article-title>
. <source>Neurology</source>
<volume>73</volume>
: <fpage>1451</fpage>
–<lpage>1456</lpage>
<pub-id pub-id-type="pmid">19884572</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Miller1"><label>56</label>
<mixed-citation publication-type="journal"><name><surname>Miller</surname>
<given-names>TD</given-names>
</name>
, <name><surname>Jackson</surname>
<given-names>AP</given-names>
</name>
, <name><surname>Barresi</surname>
<given-names>R</given-names>
</name>
, <name><surname>Smart</surname>
<given-names>CM</given-names>
</name>
, <name><surname>Eugenicos</surname>
<given-names>M</given-names>
</name>
, <etal>et al</etal>
(<year>2009</year>
) <article-title>Inclusion body myopathy with Paget disease and frontotemporal dementia (IBMPFD): clinical features including sphincter disturbance in a large pedigree</article-title>
. <source>J Neurol Neurosurg Psychiatry</source>
<volume>80</volume>
: <fpage>583</fpage>
–<lpage>584</lpage>
<pub-id pub-id-type="pmid">19372299</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Farrer1"><label>57</label>
<mixed-citation publication-type="journal"><name><surname>Farrer</surname>
<given-names>MJ</given-names>
</name>
, <name><surname>Hulihan</surname>
<given-names>MM</given-names>
</name>
, <name><surname>Kachergus</surname>
<given-names>JM</given-names>
</name>
, <name><surname>Dachsel</surname>
<given-names>JC</given-names>
</name>
, <name><surname>Stoessl</surname>
<given-names>AJ</given-names>
</name>
, <etal>et al</etal>
(<year>2009</year>
) <article-title>DCTN1 mutations in Perry syndrome</article-title>
. <source>Nat Genet</source>
<volume>41</volume>
: <fpage>163</fpage>
–<lpage>165</lpage>
<pub-id pub-id-type="pmid">19136952</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Wider1"><label>58</label>
<mixed-citation publication-type="journal"><name><surname>Wider</surname>
<given-names>C</given-names>
</name>
, <name><surname>Dickson</surname>
<given-names>DW</given-names>
</name>
, <name><surname>Stoessl</surname>
<given-names>AJ</given-names>
</name>
, <name><surname>Tsuboi</surname>
<given-names>Y</given-names>
</name>
, <name><surname>Chapon</surname>
<given-names>F</given-names>
</name>
, <etal>et al</etal>
(<year>2009</year>
) <article-title>Pallidonigral TDP-43 pathology in Perry syndrome</article-title>
. <source>Parkinsonism Relat Disord</source>
<volume>15</volume>
: <fpage>281</fpage>
–<lpage>286</lpage>
<pub-id pub-id-type="pmid">18723384</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-VanGerpen1"><label>59</label>
<mixed-citation publication-type="journal"><name><surname>Van Gerpen</surname>
<given-names>JA</given-names>
</name>
, <name><surname>Ledoux</surname>
<given-names>MS</given-names>
</name>
, <name><surname>Wszolek</surname>
<given-names>ZK</given-names>
</name>
(<year>2010</year>
) <article-title>Adult-onset leg dystonia due to a missense mutation in THAP1</article-title>
. <source>Mov Disord</source>
<volume>25</volume>
: <fpage>1306</fpage>
–<lpage>1307</lpage>
<pub-id pub-id-type="pmid">20629133</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Ledoux1"><label>60</label>
<mixed-citation publication-type="journal"><name><surname>Ledoux</surname>
<given-names>MS</given-names>
</name>
, <name><surname>Xiao</surname>
<given-names>J</given-names>
</name>
, <name><surname>Rudzinska</surname>
<given-names>M</given-names>
</name>
, <name><surname>Bastian</surname>
<given-names>RW</given-names>
</name>
, <name><surname>Wszolek</surname>
<given-names>ZK</given-names>
</name>
, <etal>et al</etal>
(<year>2012</year>
) <article-title>Genotype-phenotype correlations in THAP1 dystonia: Molecular foundations and description of new cases</article-title>
. <source>Parkinsonism Relat Disord</source>
</mixed-citation>
</ref>
<ref id="pone.0043099-Hayflick1"><label>61</label>
<mixed-citation publication-type="journal"><name><surname>Hayflick</surname>
<given-names>L</given-names>
</name>
, <name><surname>Moorhead</surname>
<given-names>PS</given-names>
</name>
(<year>1961</year>
) <article-title>The serial cultivation of human diploid cell strains</article-title>
. <source>Exp Cell Res</source>
<volume>25</volume>
: <fpage>585</fpage>
–<lpage>621</lpage>
</mixed-citation>
</ref>
<ref id="pone.0043099-Kitada2"><label>62</label>
<mixed-citation publication-type="journal"><name><surname>Kitada</surname>
<given-names>M</given-names>
</name>
, <name><surname>Wakao</surname>
<given-names>S</given-names>
</name>
, <name><surname>Dezawa</surname>
<given-names>M</given-names>
</name>
(<year>2012</year>
) <article-title>Muse cells and induced pluripotent stem cell: implication of the elite model</article-title>
. <source>Cell Mol Life Sci</source>
</mixed-citation>
</ref>
<ref id="pone.0043099-Wakao1"><label>63</label>
<mixed-citation publication-type="journal"><name><surname>Wakao</surname>
<given-names>S</given-names>
</name>
, <name><surname>Kitada</surname>
<given-names>M</given-names>
</name>
, <name><surname>Kuroda</surname>
<given-names>Y</given-names>
</name>
, <name><surname>Shigemoto</surname>
<given-names>T</given-names>
</name>
, <name><surname>Matsuse</surname>
<given-names>D</given-names>
</name>
, <etal>et al</etal>
(<year>2011</year>
) <article-title>Multilineage-differentiating stress-enduring (Muse) cells are a primary source of induced pluripotent stem cells in human fibroblasts</article-title>
. <source>Proc Natl Acad Sci U S A</source>
<volume>108</volume>
: <fpage>9875</fpage>
–<lpage>9880</lpage>
<pub-id pub-id-type="pmid">21628574</pub-id>
</mixed-citation>
</ref>
<ref id="pone.0043099-Feng1"><label>64</label>
<mixed-citation publication-type="journal"><name><surname>Feng</surname>
<given-names>B</given-names>
</name>
, <name><surname>Ng</surname>
<given-names>JH</given-names>
</name>
, <name><surname>Heng</surname>
<given-names>JC</given-names>
</name>
, <name><surname>Ng</surname>
<given-names>HH</given-names>
</name>
(<year>2009</year>
) <article-title>Molecules that promote or enhance reprogramming of somatic cells to induced pluripotent stem cells</article-title>
. <source>Cell Stem Cell</source>
<volume>4</volume>
: <fpage>301</fpage>
–<lpage>312</lpage>
<pub-id pub-id-type="pmid">19341620</pub-id>
</mixed-citation>
</ref>
</ref-list>
</back>
</pmc>
</record>
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