The Neurodegenerative Disease Protein Ataxin-1 Antagonizes the Neuronal Survival Function of Myocyte Enhancer Factor-2
Open Access
- 1 October 2007
- journal article
- Published by Elsevier BV
- Vol. 282 (40), 29186-29192
- https://doi.org/10.1074/jbc.m704182200
Abstract
No abstract availableThis publication has 31 references indexed in Scilit:
- ATAXIN-1 Interacts with the Repressor Capicua in Its Native Complex to Cause SCA1 NeuropathologyCell, 2006
- A century-old debate on protein aggregation and neurodegeneration enters the clinicNature, 2006
- Polyglutamine is Not All: The Functional Role of the AXH Domain in the Ataxin-1 ProteinJournal of Molecular Biology, 2005
- Boat, an AXH domain protein, suppresses the cytotoxicity of mutant ataxin-1The EMBO Journal, 2005
- 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 of the United States of America, 2004
- Pathogenesis of polyglutamine disorders: aggregation revisitedHuman Molecular Genetics, 2003
- Serine 776 of Ataxin-1 Is Critical for Polyglutamine-Induced Disease in SCA1 Transgenic MiceNeuron, 2003
- SCA1 molecular genetics: a history of a 13 year collaboration against glutaminesHuman Molecular Genetics, 2001
- Identification of genes that modify ataxin-1-induced neurodegenerationNature, 2000
- Identification and characterization of the gene causing type 1 spinocerebellar ataxiaNature Genetics, 1994