Ataxin-10, the Spinocerebellar Ataxia Type 10 Neurodegenerative Disorder Protein, Is Essential for Survival of Cerebellar Neurons
Open Access
- 1 August 2004
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 279 (34) , 35542-35550
- https://doi.org/10.1074/jbc.m405865200
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesisThe Lancet Neurology, 2004
- Ataxin 1, a SCA1 neurodegenerative disorder protein, is functionally linked to the silencing mediator of retinoid and thyroid hormone receptorsProceedings of the National Academy of Sciences, 2004
- Elucidation of ataxin-3 and ataxin-7 function by integrative bioinformaticsHuman Molecular Genetics, 2003
- Ataxin-3 Is a Histone-binding Protein with Two Independent Transcriptional Corepressor ActivitiesJournal of Biological Chemistry, 2002
- Dominantly inherited, non-coding microsatellite expansion disordersCurrent Opinion in Genetics & Development, 2002
- Expansion explosion: new clues to the pathogenesis of repeat expansion neurodegenerative diseasesTrends in Molecular Medicine, 2001
- Sticky DNA, a Self-associated Complex Formed at Long GAA·TTC Repeats in Intron 1 of the Frataxin Gene, Inhibits TranscriptionJournal of Biological Chemistry, 2001
- Spinocerebellar AtaxiasNeurobiology of Disease, 2000
- Glutamine Repeats and NeurodegenerationAnnual Review of Neuroscience, 2000
- Regulation of Mitochondrial Iron Accumulation by Yfh1p, a Putative Homolog of FrataxinScience, 1997