Mouse models of Huntington's disease
- 1 January 2002
- journal article
- review article
- Published by Elsevier in Trends in Pharmacological Sciences
- Vol. 23 (1) , 32-39
- https://doi.org/10.1016/s0165-6147(00)01884-8
Abstract
No abstract availableKeywords
This publication has 63 references indexed in Scilit:
- Inactivation of Hdh in the brain and testis results in progressive neurodegeneration and sterility in miceNature Genetics, 2000
- Fourteen and counting: unraveling trinucleotide repeat diseasesHuman Molecular Genetics, 2000
- Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington’s diseaseNeurology, 1999
- Huntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansionNature Genetics, 1997
- Increased apoptosis and early embryonic lethality in mice nullizygous for the Huntington's disease gene homologueNature Genetics, 1995
- Identification and localization of huntingtin in brain and human lymphoblastoid cell lines with anti-fusion protein antibodies.Proceedings of the National Academy of Sciences, 1995
- Inactivation of the Mouse Huntington's Disease Gene Homolog HdhScience, 1995
- Targeted disruption of the Huntington's disease gene results in embryonic lethality and behavioral and morphological changes in heterozygotesCell, 1995
- A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomesCell, 1993
- Neuropathological Classification of Huntingtonʼs DiseaseJournal of Neuropathology and Experimental Neurology, 1985