Huntington's disease: Dancing in a dish
Identifieur interne : 000106 ( Ncbi/Merge ); précédent : 000105; suivant : 000107Huntington's disease: Dancing in a dish
Auteurs : Kejing Zhang [États-Unis] ; Fei Yi [États-Unis] ; Guang-Hui Liu [États-Unis, République populaire de Chine] ; Juan Carlos Izpisua Belmonte [États-Unis, Espagne]Source :
- Cell Research [ 1001-0602 ] ; 2012.
Abstract
In a recent landmark paper, the Huntington's disease (HD) iPSC Consortium reports on the establishment and characterization of a panel of iPSC lines from HD patients, and more importantly, the successful modeling of HD
Url:
DOI: 10.1038/cr.2012.116
PubMed: 22868272
PubMed Central: 3515752
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<front><div type="abstract" xml:lang="en"><p>In a recent landmark paper, the Huntington's disease (HD) iPSC Consortium reports on the establishment and characterization of a panel of iPSC lines from HD patients, and more importantly, the successful modeling of HD <italic>in vitro</italic>
. In the same issue of <italic>Cell Stem Cell</italic>
, An <italic>et al</italic>
. reports on the successful targeted gene correction of HD in human iPSCs. Both advances are exciting, provide new resources for current and future HD research, and uncover new challenges to better understand and, most importantly, treat this devastating disease in the near future.</p>
</div>
</front>
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<pmc article-type="other"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Cell Res</journal-id>
<journal-id journal-id-type="iso-abbrev">Cell Res</journal-id>
<journal-title-group><journal-title>Cell Research</journal-title>
</journal-title-group>
<issn pub-type="ppub">1001-0602</issn>
<issn pub-type="epub">1748-7838</issn>
<publisher><publisher-name>Nature Publishing Group</publisher-name>
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<article-meta><article-id pub-id-type="pmid">22868272</article-id>
<article-id pub-id-type="pmc">3515752</article-id>
<article-id pub-id-type="pii">cr2012116</article-id>
<article-id pub-id-type="doi">10.1038/cr.2012.116</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Research Highlight</subject>
</subj-group>
</article-categories>
<title-group><article-title>Huntington's disease: Dancing in a dish</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Zhang</surname>
<given-names>Kejing</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
<xref ref-type="author-notes" rid="note1"><sup>*</sup>
</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Yi</surname>
<given-names>Fei</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
<xref ref-type="author-notes" rid="note1"><sup>*</sup>
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<contrib contrib-type="author"><name><surname>Liu</surname>
<given-names>Guang-Hui</given-names>
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<xref ref-type="aff" rid="aff1">1</xref>
<xref ref-type="aff" rid="aff2">2</xref>
<xref ref-type="corresp" rid="caf1">*</xref>
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<contrib contrib-type="author"><name><surname>Belmonte</surname>
<given-names>Juan Carlos Izpisua</given-names>
</name>
<xref ref-type="aff" rid="aff1">1</xref>
<xref ref-type="aff" rid="aff3">3</xref>
<xref ref-type="corresp" rid="caf2">*</xref>
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<aff id="aff1"><label>1</label>
<institution>Gene Expression Laboratory, Salk Institute for Biological Studies</institution>
, 10010 North Torrey Pines Road, La Jolla, CA 92037,<country>USA</country>
</aff>
<aff id="aff2"><label>2</label>
<institution>National Laboratory of Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences</institution>
, Beijing 100101,<country>China</country>
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<aff id="aff3"><label>3</label>
<institution>Center for Regenerative Medicine in Barcelona</institution>
, Dr. Aiguader 88, 08003 Barcelona,<country>Spain</country>
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<author-notes><corresp id="caf1"><label>*</label>
E-mail: <email>ghliu@ibp.ac.cn</email>
</corresp>
<corresp id="caf2"><label>*</label>
E-mail: <email>belmonte@salk.edu</email>
, <email>izpisua@cmrb.eu</email>
</corresp>
<fn fn-type="present-address" id="note1"><label>*</label>
<p>These two authors contributed equally to this work.</p>
</fn>
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<pub-date pub-type="ppub"><month>12</month>
<year>2012</year>
</pub-date>
<pub-date pub-type="epub"><day>07</day>
<month>08</month>
<year>2012</year>
</pub-date>
<volume>22</volume>
<issue>12</issue>
<fpage>1627</fpage>
<lpage>1630</lpage>
<permissions><copyright-statement>Copyright © 2012 Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences</copyright-statement>
<copyright-year>2012</copyright-year>
<copyright-holder>Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences</copyright-holder>
</permissions>
<abstract abstract-type="summary"><p>In a recent landmark paper, the Huntington's disease (HD) iPSC Consortium reports on the establishment and characterization of a panel of iPSC lines from HD patients, and more importantly, the successful modeling of HD <italic>in vitro</italic>
. In the same issue of <italic>Cell Stem Cell</italic>
, An <italic>et al</italic>
. reports on the successful targeted gene correction of HD in human iPSCs. Both advances are exciting, provide new resources for current and future HD research, and uncover new challenges to better understand and, most importantly, treat this devastating disease in the near future.</p>
</abstract>
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