PQBP-1 is expressed predominantly in the central nervous system during development
Author:
Publisher
Wiley
Subject
General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1460-9568.2005.04339.x/fullpdf
Reference9 articles.
1. Mutant huntingtin promotes the fibrillogenesis of wild-type huntingtin: a potential mechanism for loss of huntingtin function in Huntington's disease;Busch;J. Biol. Chem.,2003
2. Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation;Kalscheuer;Nature Genet.,2003
3. Genotype-phenotype studies in three families with mutations in the polyglutamine-binding protein 1 gene (PQBP1);Kleefstra;Clin. Genet.,2004
4. Novel truncating mutations in the polyglutamine tract binding protein 1 gene (PQBP1) cause renpenning syndrome and X-linked mental retardation in another family with microcephaly;Lenski;Am. J. Hum. Genet.,2004
5. Interaction between mutant ataxin-1 and PQBP-1 affects transcription and cell death;Okazawa;Neuron,2002
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