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Modeling neurodegeneration in zebrafish.

Identifieur interne : 000C09 ( PubMed/Corpus ); précédent : 000C08; suivant : 000C10

Modeling neurodegeneration in zebrafish.

Auteurs : Yanwei Xi ; Sandra Noble ; Marc Ekker

Source :

RBID : pubmed:21271309

English descriptors

Abstract

The zebrafish, Danio rerio, has been established as an excellent vertebrate model for the study of developmental biology and gene function. It also has proven to be a valuable model to study human diseases. Here, we reviewed recent publications using zebrafish to study the pathology of human neurodegenerative diseases including Parkinson's, Huntington's, and Alzheimer's. These studies indicate that zebrafish genes and their human homologues have conserved functions with respect to the etiology of neurodegenerative diseases. The characteristics of the zebrafish and the experimental approaches to which it is amenable make this species a useful complement to other animal models for the study of pathologic mechanisms of neurodegenerative diseases and for the screening of compounds with therapeutic potential.

DOI: 10.1007/s11910-011-0182-2
PubMed: 21271309

Links to Exploration step

pubmed:21271309

Le document en format XML

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<CommentsCorrectionsList>
<CommentsCorrections RefType="Cites">
<RefSource>Development. 2008 May;135(10):1735-43</RefSource>
<PMID Version="1">18403413</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Gene. 1998 Sep 14;217(1-2):117-25</RefSource>
<PMID Version="1">9795179</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Biochemistry. 1999 Oct 12;38(41):13602-9</RefSource>
<PMID Version="1">10521267</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Neurosci. 2010 Feb 3;30(5):1788-97</RefSource>
<PMID Version="1">20130188</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Dev Biol. 2009 Nov 1;335(1):1-11</RefSource>
<PMID Version="1">19664615</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Brain. 2009 Jun;132(Pt 6):1613-23</RefSource>
<PMID Version="1">19439422</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Biol Chem. 2007 Mar 23;282(12):9195-203</RefSource>
<PMID Version="1">17170113</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Mol Neurodegener. 2009 Feb 25;4:12</RefSource>
<PMID Version="1">19243613</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Science. 2009 Jun 5;324(5932):1327-30</RefSource>
<PMID Version="1">19498170</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Proc Natl Acad Sci U S A. 2007 Jul 3;104(27):11441-6</RefSource>
<PMID Version="1">17563363</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Neuron. 2010 Jun 10;66(5):646-61</RefSource>
<PMID Version="1">20547124</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Dev Biol. 2008 Feb 1;314(1):84-92</RefSource>
<PMID Version="1">18164283</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Proc Natl Acad Sci U S A. 2005 May 31;102(22):8024-9</RefSource>
<PMID Version="1">15911761</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Proc Natl Acad Sci U S A. 2003 Apr 1;100(7):4078-83</RefSource>
<PMID Version="1">12642658</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Nat Genet. 2007 Feb;39(2):168-77</RefSource>
<PMID Version="1">17220890</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Neurochem. 2009 Feb;108(3):719-31</RefSource>
<PMID Version="1">19046410</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Dev Genes Evol. 2002 Nov;212(10):486-90</RefSource>
<PMID Version="1">12424519</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Proc Natl Acad Sci U S A. 2000 Oct 10;97(21):11403-8</RefSource>
<PMID Version="1">11027340</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Nat Genet. 1995 Oct;11(2):155-63</RefSource>
<PMID Version="1">7550343</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Neurochem. 2004 Jan;88(2):443-53</RefSource>
<PMID Version="1">14690532</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Proc Natl Acad Sci U S A. 2005 Sep 20;102(38):13461-6</RefSource>
<PMID Version="1">16174740</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Proc Natl Acad Sci U S A. 2008 Aug 12;105(32):11364-9</RefSource>
<PMID Version="1">18687901</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Neurosci. 2009 Feb 4;29(5):1343-9</RefSource>
<PMID Version="1">19193881</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Neurobiol Aging. 2011 Nov;32(11):1994-2005</RefSource>
<PMID Version="1">20060621</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Biochem Biophys Res Commun. 2003 Dec 19;312(3):601-7</RefSource>
<PMID Version="1">14680807</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Development. 1996 Dec;123:37-46</RefSource>
<PMID Version="1">9007227</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Brain Res Bull. 2002 Feb-Mar 1;57(3-4):385-7</RefSource>
<PMID Version="1">11922994</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Neurosci. 2008 Aug 13;28(33):8199-207</RefSource>
<PMID Version="1">18701682</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Eur J Neurosci. 2005 Mar;21(6):1758-62</RefSource>
<PMID Version="1">15845104</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Brain Res. 2006 Oct 3;1113(1):33-44</RefSource>
<PMID Version="1">16942755</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Neurosci. 2009 Sep 9;29(36):11257-62</RefSource>
<PMID Version="1">19741132</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Science. 1985 Feb 15;227(4688):770-3</RefSource>
<PMID Version="1">3155875</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>PLoS One. 2010;5(7):e11783</RefSource>
<PMID Version="1">20689587</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Hum Mol Genet. 2009 Dec 15;18(24):4830-42</RefSource>
<PMID Version="1">19797250</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Neurochem. 2007 Mar;100(6):1626-35</RefSource>
<PMID Version="1">17166173</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Neurotoxicol Teratol. 2004 Nov-Dec;26(6):857-64</RefSource>
<PMID Version="1">15451049</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Eur J Neurosci. 2010 Feb;31(4):623-33</RefSource>
<PMID Version="1">20141529</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Ir J Med Sci. 1994 May;163(5):236-7</RefSource>
<PMID Version="1">8045729</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>PLoS Genet. 2010 Apr;6(4):e1000914</RefSource>
<PMID Version="1">20421934</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Neurosci Res. 2002 Dec 15;70(6):734-45</RefSource>
<PMID Version="1">12444595</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Clin Invest. 2009 May;119(5):1382-95</RefSource>
<PMID Version="1">19363289</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Nat Neurosci. 2009 Jul;12(7):826-8</RefSource>
<PMID Version="1">19503083</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Proc Natl Acad Sci U S A. 2008 Feb 19;105(7):2693-8</RefSource>
<PMID Version="1">18258746</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Nature. 2006 Jun 29;441(7097):1157-61</RefSource>
<PMID Version="1">16672980</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Proc Natl Acad Sci U S A. 1997 Aug 5;94(16):8622-7</RefSource>
<PMID Version="1">9238027</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Nature. 2006 Jun 29;441(7097):1162-6</RefSource>
<PMID Version="1">16672981</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Brain Res Mol Brain Res. 2005 Nov 30;141(2):128-37</RefSource>
<PMID Version="1">16209898</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Dev Genes Evol. 2001 Dec;211(11):563-7</RefSource>
<PMID Version="1">11862463</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Nat Chem Biol. 2008 May;4(5):295-305</RefSource>
<PMID Version="1">18391949</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Neurobiol Dis. 2010 Oct;40(1):93-101</RefSource>
<PMID Version="1">20600915</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Mech Dev. 2002 Oct;118(1-2):91-8</RefSource>
<PMID Version="1">12351173</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Hum Mol Genet. 2007 Aug 15;16(16):1905-20</RefSource>
<PMID Version="1">17567778</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Hum Mol Genet. 1999 Mar;8(3):397-407</RefSource>
<PMID Version="1">9949199</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Nucleic Acids Res. 2007;35(19):6501-16</RefSource>
<PMID Version="1">17897967</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Clin Exp Neuropsychol. 2007 May;29(4):395-404</RefSource>
<PMID Version="1">17497563</PMID>
</CommentsCorrections>
</CommentsCorrectionsList>
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   |texte=   Modeling neurodegeneration in zebrafish.
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