Spinal and bulbar muscular atrophy: ligand-dependent pathogenesis and therapeutic perspectives
- 27 February 2004
- journal article
- review article
- Published by Springer Nature in Journal of Molecular Medicine
- Vol. 82 (5) , 298-307
- https://doi.org/10.1007/s00109-004-0530-7
Abstract
No abstract availableKeywords
This publication has 97 references indexed in Scilit:
- Ligand Promotes Intranuclear Inclusions in a Novel Cell Model of Spinal and Bulbar Muscular AtrophyJournal of Biological Chemistry, 2002
- Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the worldEuropean Journal of Human Genetics, 2001
- Chaperones Hsp70 and Hsp40 Suppress Aggregate Formation and Apoptosis in Cultured Neuronal Cells Expressing Truncated Androgen Receptor Protein with Expanded Polyglutamine TractJournal of Biological Chemistry, 2000
- Caspase-3 Cleaves the Expanded Androgen Receptor Protein of Spinal and Bulbar Muscular Atrophy in a Polyglutamine Repeat Length-Dependent MannerBiochemical and Biophysical Research Communications, 1998
- Nonneural Nuclear Inclusions of Androgen Receptor Protein in Spinal and Bulbar Muscular AtrophyThe American Journal of Pathology, 1998
- Characterization of an Expanded Glutamine Repeat Androgen Receptor in a Neuronal Cell Culture SystemNeurobiology of Disease, 1997
- Aggregation of Huntingtin in Neuronal Intranuclear Inclusions and Dystrophic Neurites in BrainScience, 1997
- Exon 1 of the HD Gene with an Expanded CAG Repeat Is Sufficient to Cause a Progressive Neurological Phenotype in Transgenic MiceCell, 1996
- Central motor and sensory conduction in X-linked recessive bulbospinal neuronopathy.Journal of Neurology, Neurosurgery & Psychiatry, 1992
- Proximal spinal muscular atrophy.Journal of Neurology, Neurosurgery & Psychiatry, 1966