Expression and distribution of the dentatorubral-pallidoluysian atrophy gene product (atrophin-1/drplap) in neuronal and non-neuronal tissues
- 27 February 1997
- journal article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 146 (1) , 19-26
- https://doi.org/10.1016/s0022-510x(96)00266-3
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDHNature Medicine, 1996
- Molecular re-investigation of patients with Huntington's disease in Wessex reveals a family with dentatorubral and pallidoluysian atrophyHuman Genetics, 1996
- SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeatCell, 1995
- Comparative sequence analysis of the human and pufferfish Huntington's disease genesNature Genetics, 1995
- Huntingtin is a cytoplasmic protein associated with vesicles in human and rat brain neuronsNeuron, 1995
- The Haw River Syndrome: Dentatorubropallidoluysian atrophy (DRPLA) in an African–American familyNature Genetics, 1994
- Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA)Nature Genetics, 1994
- Evolution of NeocortexPublished by Springer Nature ,1990
- Substance P and somatostatin coexist within neuritic plaques: Implications for the pathogenesis of Alzheimer's diseaseNeuroscience, 1989
- Individual exons encode the integral membrane domains of human myelin proteolipid protein.Proceedings of the National Academy of Sciences, 1986