Cargando…
A selective inhibitor of histone deacetylase 3 prevents cognitive deficits and suppresses striatal CAG repeat expansions in Huntington’s disease mice
Huntington’s disease (HD) is a neurodegenerative disorder whose major symptoms include progressive motor and cognitive dysfunction. Cognitive decline is a critical quality of life concern for HD patients and families. The enzyme histone deacetylase 3 (HDAC3) appears to be important in HD pathology b...
Autores principales: | Suelves, Nuria, Kirkham-McCarthy, Lucy, Lahue, Robert S., Ginés, Silvia |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5519595/ https://www.ncbi.nlm.nih.gov/pubmed/28729730 http://dx.doi.org/10.1038/s41598-017-05125-2 |
Ejemplares similares
-
Histone Deacetylase Complexes Promote Trinucleotide Repeat Expansions
por: Debacker, Kim, et al.
Publicado: (2012) -
MutSβ and histone deacetylase complexes promote expansions of trinucleotide repeats in human cells
por: Gannon, Anne-Marie M., et al.
Publicado: (2012) -
Association between Age and Striatal Volume Stratified by CAG Repeat Length in Prodromal Huntington Disease
por: Aylward, Elizabeth, et al.
Publicado: (2011) -
Histone deacetylase knockouts modify transcription, CAG instability and nuclear pathology in Huntington disease mice
por: Kovalenko, Marina, et al.
Publicado: (2020) -
Huntington’s disease mouse models: unraveling the pathology caused by CAG repeat expansion
por: Kaye, Julia, et al.
Publicado: (2021)