Links to Exploration step
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Semi-quantitative PCR based screening of α-Synuclein multiplication in multiple system atrophy</title><author><name sortKey="Lincoln, Sarah J" sort="Lincoln, Sarah J" uniqKey="Lincoln S" first="Sarah J." last="Lincoln">Sarah J. Lincoln</name><affiliation><nlm:aff id="A1"> Department of Neuroscience, Mayo Clinic College of Medicine, Jacksonville, Florida</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="A1"> Department of Neuroscience, Mayo Clinic College of Medicine, Jacksonville, Florida</nlm:aff></affiliation></author><author><name sortKey="Milkovic, Nicole M" sort="Milkovic, Nicole M" uniqKey="Milkovic N" first="Nicole M." last="Milkovic">Nicole M. Milkovic</name><affiliation><nlm:aff id="A1"> Department of Neuroscience, Mayo Clinic College of Medicine, Jacksonville, Florida</nlm:aff></affiliation></author><author><name sortKey="Dickson, Dennis W" sort="Dickson, Dennis W" uniqKey="Dickson D" first="Dennis W." last="Dickson">Dennis W. Dickson</name><affiliation><nlm:aff id="A2"> Department of Pathology, Mayo Clinic College of Medicine, Jacksonville, Florida</nlm:aff></affiliation></author><author><name sortKey="Rajput, Alex" sort="Rajput, Alex" uniqKey="Rajput A" first="Alex" last="Rajput">Alex Rajput</name><affiliation><nlm:aff id="A3"> Division of Neurology, University of Saskatchewan and Saskatoon Health Region, Saskatoon, Saskatchewan, Canada</nlm:aff></affiliation><affiliation><nlm:aff id="A5"> Saskatchewan Center for Parkinson’s disease and Movement Disorders, Royal University Hospital, Saskatoon, Saskatchewan Canada</nlm:aff></affiliation></author><author><name sortKey="Robinson, Christopher A" sort="Robinson, Christopher A" uniqKey="Robinson C" first="Christopher A." last="Robinson">Christopher A. Robinson</name><affiliation><nlm:aff id="A4"> Department of Pathology, University of Saskatchewan and Saskatoon Health Region, Saskatoon, Saskatchewan, Canada</nlm:aff></affiliation><affiliation><nlm:aff id="A5"> Saskatchewan Center for Parkinson’s disease and Movement Disorders, Royal University Hospital, Saskatoon, Saskatchewan Canada</nlm:aff></affiliation></author><author><name sortKey="Papapetropoulos, Spiridon" sort="Papapetropoulos, Spiridon" uniqKey="Papapetropoulos S" first="Spiridon" last="Papapetropoulos">Spiridon Papapetropoulos</name><affiliation><nlm:aff id="A6"> Department of Neurology, University of Miami, Miller School of Medicine, Miami, Florida</nlm:aff></affiliation></author><author><name sortKey="Mash, Deborah C" sort="Mash, Deborah C" uniqKey="Mash D" first="Deborah C." last="Mash">Deborah C. Mash</name><affiliation><nlm:aff id="A6"> Department of Neurology, University of Miami, Miller School of Medicine, Miami, Florida</nlm:aff></affiliation></author><author><name sortKey="Farrer, Matthew J" sort="Farrer, Matthew J" uniqKey="Farrer M" first="Matthew J." last="Farrer">Matthew J. Farrer</name><affiliation><nlm:aff id="A1"> Department of Neuroscience, Mayo Clinic College of Medicine, Jacksonville, Florida</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">17291816</idno><idno type="pmc">2269731</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2269731</idno><idno type="RBID">PMC:2269731</idno><idno type="doi">10.1016/j.parkreldis.2006.12.005</idno><date when="2007">2007</date><idno type="wicri:Area/Pmc/Corpus">000904</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000904</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Semi-quantitative PCR based screening of α-Synuclein multiplication in multiple system atrophy</title><author><name sortKey="Lincoln, Sarah J" sort="Lincoln, Sarah J" uniqKey="Lincoln S" first="Sarah J." last="Lincoln">Sarah J. Lincoln</name><affiliation><nlm:aff id="A1"> Department of Neuroscience, Mayo Clinic College of Medicine, Jacksonville, Florida</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="A1"> Department of Neuroscience, Mayo Clinic College of Medicine, Jacksonville, Florida</nlm:aff></affiliation></author><author><name sortKey="Milkovic, Nicole M" sort="Milkovic, Nicole M" uniqKey="Milkovic N" first="Nicole M." last="Milkovic">Nicole M. Milkovic</name><affiliation><nlm:aff id="A1"> Department of Neuroscience, Mayo Clinic College of Medicine, Jacksonville, Florida</nlm:aff></affiliation></author><author><name sortKey="Dickson, Dennis W" sort="Dickson, Dennis W" uniqKey="Dickson D" first="Dennis W." last="Dickson">Dennis W. Dickson</name><affiliation><nlm:aff id="A2"> Department of Pathology, Mayo Clinic College of Medicine, Jacksonville, Florida</nlm:aff></affiliation></author><author><name sortKey="Rajput, Alex" sort="Rajput, Alex" uniqKey="Rajput A" first="Alex" last="Rajput">Alex Rajput</name><affiliation><nlm:aff id="A3"> Division of Neurology, University of Saskatchewan and Saskatoon Health Region, Saskatoon, Saskatchewan, Canada</nlm:aff></affiliation><affiliation><nlm:aff id="A5"> Saskatchewan Center for Parkinson’s disease and Movement Disorders, Royal University Hospital, Saskatoon, Saskatchewan Canada</nlm:aff></affiliation></author><author><name sortKey="Robinson, Christopher A" sort="Robinson, Christopher A" uniqKey="Robinson C" first="Christopher A." last="Robinson">Christopher A. Robinson</name><affiliation><nlm:aff id="A4"> Department of Pathology, University of Saskatchewan and Saskatoon Health Region, Saskatoon, Saskatchewan, Canada</nlm:aff></affiliation><affiliation><nlm:aff id="A5"> Saskatchewan Center for Parkinson’s disease and Movement Disorders, Royal University Hospital, Saskatoon, Saskatchewan Canada</nlm:aff></affiliation></author><author><name sortKey="Papapetropoulos, Spiridon" sort="Papapetropoulos, Spiridon" uniqKey="Papapetropoulos S" first="Spiridon" last="Papapetropoulos">Spiridon Papapetropoulos</name><affiliation><nlm:aff id="A6"> Department of Neurology, University of Miami, Miller School of Medicine, Miami, Florida</nlm:aff></affiliation></author><author><name sortKey="Mash, Deborah C" sort="Mash, Deborah C" uniqKey="Mash D" first="Deborah C." last="Mash">Deborah C. Mash</name><affiliation><nlm:aff id="A6"> Department of Neurology, University of Miami, Miller School of Medicine, Miami, Florida</nlm:aff></affiliation></author><author><name sortKey="Farrer, Matthew J" sort="Farrer, Matthew J" uniqKey="Farrer M" first="Matthew J." last="Farrer">Matthew J. Farrer</name><affiliation><nlm:aff id="A1"> Department of Neuroscience, Mayo Clinic College of Medicine, Jacksonville, Florida</nlm:aff></affiliation></author></analytic><series><title level="j">Parkinsonism & related disorders</title><idno type="ISSN">1353-8020</idno><imprint><date when="2007">2007</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p id="P2">Multiple system atrophy (MSA) is by nature a ‘sporadic’ disease with no evidence of familial aggregation observed. However the <italic>SNCA</italic> multiplication families have clinically displayed parkinsonism and autonomic dysfunction. The present study did not find any <italic>SNCA</italic> multiplications in a series of 58 pathologically confirmed MSA cases excluding this event as a common cause of MSA. The question of a genetic component in MSA remains to be answered.</p></div></front></TEI><pmc article-type="research-article"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<pmc-dir>properties manuscript</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-journal-id">9513583</journal-id><journal-id journal-id-type="pubmed-jr-id">21522</journal-id><journal-id journal-id-type="nlm-ta">Parkinsonism Relat Disord</journal-id><journal-title>Parkinsonism & related disorders</journal-title><issn pub-type="ppub">1353-8020</issn></journal-meta><article-meta><article-id pub-id-type="pmid">17291816</article-id><article-id pub-id-type="pmc">2269731</article-id><article-id pub-id-type="doi">10.1016/j.parkreldis.2006.12.005</article-id><article-id pub-id-type="manuscript">NIHMS29719</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Semi-quantitative PCR based screening of α-Synuclein multiplication in multiple system atrophy</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Lincoln</surname><given-names>Sarah J.</given-names></name><xref rid="A1" ref-type="aff">1</xref></contrib><contrib contrib-type="author"><name><surname>Ross</surname><given-names>Owen A.</given-names></name><xref rid="A1" ref-type="aff">1</xref><xref rid="FN1" ref-type="author-notes">*</xref></contrib><contrib contrib-type="author"><name><surname>Milkovic</surname><given-names>Nicole M.</given-names></name><xref rid="A1" ref-type="aff">1</xref></contrib><contrib contrib-type="author"><name><surname>Dickson</surname><given-names>Dennis W.</given-names></name><xref rid="A2" ref-type="aff">2</xref></contrib><contrib contrib-type="author"><name><surname>Rajput</surname><given-names>Alex</given-names></name><xref rid="A3" ref-type="aff">3</xref><xref rid="A5" ref-type="aff">5</xref></contrib><contrib contrib-type="author"><name><surname>Robinson</surname><given-names>Christopher A.</given-names></name><xref rid="A4" ref-type="aff">4</xref><xref rid="A5" ref-type="aff">5</xref></contrib><contrib contrib-type="author"><name><surname>Papapetropoulos</surname><given-names>Spiridon</given-names></name><xref rid="A6" ref-type="aff">6</xref></contrib><contrib contrib-type="author"><name><surname>Mash</surname><given-names>Deborah C.</given-names></name><xref rid="A6" ref-type="aff">6</xref></contrib><contrib contrib-type="author"><name><surname>Farrer</surname><given-names>Matthew J.</given-names></name><xref rid="A1" ref-type="aff">1</xref></contrib></contrib-group><aff id="A1"><label>1</label> Department of Neuroscience, Mayo Clinic College of Medicine, Jacksonville, Florida</aff><aff id="A2"><label>2</label> Department of Pathology, Mayo Clinic College of Medicine, Jacksonville, Florida</aff><aff id="A3"><label>3</label> Division of Neurology, University of Saskatchewan and Saskatoon Health Region, Saskatoon, Saskatchewan, Canada</aff><aff id="A4"><label>4</label> Department of Pathology, University of Saskatchewan and Saskatoon Health Region, Saskatoon, Saskatchewan, Canada</aff><aff id="A5"><label>5</label> Saskatchewan Center for Parkinson’s disease and Movement Disorders, Royal University Hospital, Saskatoon, Saskatchewan Canada</aff><aff id="A6"><label>6</label> Department of Neurology, University of Miami, Miller School of Medicine, Miami, Florida</aff><author-notes><corresp id="FN1">*Corresponding author: Owen A. Ross PhD, Molecular Genetics Laboratory and Core, Morris K. Udall Parkinson’s Disease Research Center of Excellence, Mayo Clinic, Department of Neuroscience, 4500 San Pablo Road, Jacksonville, FL 32224, Tel: (904)-953-7135, Fax: (904)-953-7370, Email: <email>ross.owen@mayo.edu</email></corresp></author-notes><pub-date pub-type="nihms-submitted"><day>26</day><month>9</month><year>2007</year></pub-date><pub-date pub-type="epub"><day>8</day><month>2</month><year>2007</year></pub-date><pub-date pub-type="ppub"><month>8</month><year>2007</year></pub-date><pub-date pub-type="pmc-release"><day>1</day><month>8</month><year>2008</year></pub-date><volume>13</volume><issue>6</issue><fpage>340</fpage><lpage>342</lpage><abstract><p id="P2">Multiple system atrophy (MSA) is by nature a ‘sporadic’ disease with no evidence of familial aggregation observed. However the <italic>SNCA</italic> multiplication families have clinically displayed parkinsonism and autonomic dysfunction. The present study did not find any <italic>SNCA</italic> multiplications in a series of 58 pathologically confirmed MSA cases excluding this event as a common cause of MSA. The question of a genetic component in MSA remains to be answered.</p></abstract><kwd-group><kwd>Semi-quantitative PCR</kwd><kwd>alpha-synuclein</kwd><kwd>genomic multiplication</kwd><kwd>multiple system atropy</kwd></kwd-group><contract-num rid="NS1">P50 NS040256-070005</contract-num><contract-num rid="NS1">P50 NS040256-07</contract-num><contract-sponsor id="NS1">National Institute of Neurological Disorders and Stroke : NINDS</contract-sponsor></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Canada/explor/ParkinsonCanadaV1/Data/Pmc/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 0009049 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Pmc/Corpus/biblio.hfd -nk 0009049 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Canada
|area= ParkinsonCanadaV1
|flux= Pmc
|étape= Corpus
|type= RBID
|clé=
|texte=
}}
| This area was generated with Dilib version V0.6.29. |  |