Machado–Joseph disease gene products carrying different carboxyl termini
- 31 August 1997
- journal article
- review article
- Published by Elsevier in Neuroscience Research
- Vol. 28 (4) , 373-377
- https://doi.org/10.1016/s0168-0102(97)00056-4
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Health, Labour and Welfare
- Research Committee for Ataxic Disease
- Ministry of Education, Culture, Sports, Science and Technology
- Japan Science and Technology Agency
This publication has 10 references indexed in Scilit:
- A polymorphic stop codon in BRCA2Nature Genetics, 1996
- Strong linkage disequilibrium and haplotype analysis in Japanese pedigrees with Machado-Joseph diseaseAmerican Journal of Medical Genetics, 1996
- Intergenerational instability of the CAG repeat of the gene for Machado- Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeatHuman Molecular Genetics, 1996
- Expanded polyglutamine in the Machado–Joseph disease protein induces cell death in vitro and in vivoNature Genetics, 1996
- Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph diseaseHuman Molecular Genetics, 1995
- CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1Nature Genetics, 1994
- The gene for Machado–Joseph disease maps to human chromosome 14qNature Genetics, 1993
- Autosomal dominant striatonigral degenerationNeurology, 1976
- Nigro-spino-dentatal degeneration with nuclear ophthalmoplegia: A unique and partially treatable clinico-pathological entityJournal of the Neurological Sciences, 1972
- Machado diseaseNeurology, 1972