Intranuclear Inclusions of Expanded Polyglutamine Protein in Spinocerebellar Ataxia Type 3
Open Access
- 1 August 1997
- journal article
- research article
- Published by Elsevier BV in Neuron
- Vol. 19 (2), 333-344
- https://doi.org/10.1016/s0896-6273(00)80943-5
Abstract
No abstract availableKeywords
This publication has 57 references indexed in Scilit:
- Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channelNature Genetics, 1997
- Exon 1 of the HD Gene with an Expanded CAG Repeat Is Sufficient to Cause a Progressive Neurological Phenotype in Transgenic MiceCell, 1996
- The expanding world of ataxinsNature Genetics, 1996
- Huntington's disease: translating a CAG repeat into a pathogenic mechanismCurrent Opinion in Neurobiology, 1996
- A huntingtin-associated protein enriched in brain with implications for pathologyNature, 1995
- Trinucleotide expansion within the MJD1 gene presents clinically as spinocerebellar ataxia and occurs most frequently in German SCA patientsHuman Molecular Genetics, 1995
- Widespread expression of Huntington's disease gene (IT15) protein productNeuron, 1995
- Gain of glutamines, gain of function?Nature Genetics, 1995
- Joseph's disease: Clinical and pathological studies in a Japanese familyAnnals of Neurology, 1986
- Neurofilament subunit–related proteins in neuronal intranuclear inclusionsAnnals of Neurology, 1984