Imperfect CAG Repeats Form Diverse Structures in SCA1 Transcripts
Open Access
- 1 October 2004
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 279 (40) , 41563-41572
- https://doi.org/10.1074/jbc.m405130200
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Beyond the Qs in the polyglutamine diseases: Table 1.Genes & Development, 2001
- Fourteen and counting: unraveling trinucleotide repeat diseasesHuman Molecular Genetics, 2000
- The intrinsically unstable life of DNA triplet repeats associated with human hereditary disordersPublished by Elsevier ,2000
- Mutation of the E6-AP Ubiquitin Ligase Reduces Nuclear Inclusion Frequency While Accelerating Polyglutamine-Induced Pathology in SCA1 MiceNeuron, 1999
- Ataxin-1 Nuclear Localization and AggregationCell, 1998
- Dynamic mutation: possible mechanisms and significance in human diseaseTrends in Biochemical Sciences, 1997
- Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structuresNature, 1997
- Identification and characterization of the gene causing type 1 spinocerebellar ataxiaNature Genetics, 1994
- Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type INature Genetics, 1993
- Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1Nature Genetics, 1993