Emerging pathogenic pathways in the spinocerebellar ataxias

This publication has 47 references indexed in Scilit:

• Polyglutamine Expansion Reduces the Association of TATA-binding Protein with DNA and Induces DNA Binding-independent Neurotoxicity
  Published by Elsevier ,2008
• Diseases of Unstable Repeat Expansion: Mechanisms and Common Principles
  Nature Reviews Genetics, 2005
• An Autosomal Dominant Cerebellar Ataxia Linked to Chromosome 16q22.1 Is Associated with a Single-Nucleotide Substitution in the 5′ Untranslated Region of the Gene Encoding a Protein with Spectrin Repeat and Rho Guanine-Nucleotide Exchange-Factor Domains
  American Journal of Human Genetics, 2005
• Polyglutamine-expanded ataxin-7 inhibits STAGA histone acetyltransferase activity to produce retinal degeneration
  Proceedings of the National Academy of Sciences, 2005
• Polyglutamine-expanded spinocerebellar ataxia-7 protein disrupts normal SAGA and SLIK histone acetyltransferase activity
  Proceedings of the National Academy of Sciences, 2005
• Linking the ubiquitin–proteasome pathway to chromatin remodeling/modification by nuclear receptors
  Journal of Molecular Endocrinology, 2005
• Rush hour at the promoter: How the ubiquitin-proteasome pathway polices the traffic flow of nuclear receptor-dependent transcription
  The Journal of Steroid Biochemistry and Molecular Biology, 2005
• An Integrative Approach to Gain Insights into the Cellular Function of Human Ataxin-2
  Journal of Molecular Biology, 2005
• Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus
  Neurology, 2004
• Gene profiling links SCA1 pathophysiology to glutamate signaling in Purkinje cells of transgenic mice
  Human Molecular Genetics, 2004