Spinal and bulbar muscular atrophy: androgen receptor dysfunction caused by a trinucleotide repeat expansion
- 29 February 1996
- journal article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 135 (2) , 149-157
- https://doi.org/10.1016/0022-510x(95)00284-9
Abstract
No abstract availableKeywords
This publication has 64 references indexed in Scilit:
- The human androgen receptor: Domain structure, genomic organization and regulation of expressionPublished by Elsevier ,2003
- Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic miceNature Genetics, 1995
- Expression of Androgen Receptor Protein within the Lumbar Spinal Cord During Ontologic Development and Following Antiandrogen Induced CryptorchidismJournal of Urology, 1994
- The Haw River Syndrome: Dentatorubropallidoluysian atrophy (DRPLA) in an African–American familyNature Genetics, 1994
- Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type INature Genetics, 1993
- Hormonal regulation of androgen receptor mRNA in the brain and anterior pituitary gland of the male ratMolecular Brain Research, 1993
- Kennedy's diseaseNeurology, 1993
- Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophyNature, 1992
- A family with adult spinal and bulbar muscular atrophy, X-linked inheritance and associated testicular failureJournal of the Neurological Sciences, 1983
- Hereditary Proximal Spinal and Bulbar Motor Neuron Disease of Late OnsetArchives of Neurology, 1982