4.6 Article

Interacting proteins as genetic modifiers of Huntington disease

期刊

TRENDS IN GENETICS
卷 23, 期 11, 页码 531-533

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ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tig.2007.07.007

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资金

  1. NIA NIH HHS [R01 AG019206, R01 AG031153] Funding Source: Medline
  2. NINDS NIH HHS [NS 045016, R01 NS041669, NS 36232, R01 NS045016, R01 NS036232] Funding Source: Medline

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Huntington disease is caused by polyglutamine expansion in huntingtin, a 350 kD protein that is ubiquitously expressed and widely distributed at the subcellular level. Recently, Kaltenbach et al. identified a large collection of novel huntingtin-interacting proteins, several of which modify mutant huntingtin toxicity in Drosophila. Thus, the interaction of mutant huntingtin with certain protein partners can influence its toxicity and therefore the severity and/or progression of Huntington disease.

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