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Mechanisms of neuronal cell death in Huntington's disease.
- Source :
-
Cytogenetic and genome research [Cytogenet Genome Res] 2003; Vol. 100 (1-4), pp. 287-95. - Publication Year :
- 2003
-
Abstract
- Huntington's disease (HD) is a genetically dominant neurodegenerative condition caused by an unique mutation in the disease gene huntingtin. Although the Huntington protein (Htt) is ubiquitously expressed, expansion of the polyglutamine tract in Htt leads to the progressive loss of specific neuronal subpopulations in HD brains. In this article, we will summarize the current understanding on mechanisms of how mutant Htt can elicit cytotoxicity, as well as how the selective sets of neuronal cell death occur in HD brains.<br /> (Copyright 2003 S. Karger AG, Basel)
- Subjects :
- Animals
Brain pathology
Cell Death
Disease Models, Animal
Humans
Huntingtin Protein
Huntington Disease pathology
Models, Biological
Mutation
Signal Transduction
Huntington Disease genetics
Nerve Tissue Proteins genetics
Neurons pathology
Nuclear Proteins genetics
Trinucleotide Repeat Expansion genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1424-859X
- Volume :
- 100
- Issue :
- 1-4
- Database :
- MEDLINE
- Journal :
- Cytogenetic and genome research
- Publication Type :
- Academic Journal
- Accession number :
- 14526190
- Full Text :
- https://doi.org/10.1159/000072864