A selective inhibitor of histone deacetylase 3 prevents cognitive deficits and suppresses striatal CAG repeat expansions in Huntington’s disease mice
Abstract 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 pa...
Guardado en:
Autores principales: | Nuria Suelves, Lucy Kirkham-McCarthy, Robert S. Lahue, Silvia Ginés |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2017
|
Materias: | |
Acceso en línea: | https://doaj.org/article/83fb75d6d54c4e1bb96e9a37f243acff |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Histone deacetylase complexes promote trinucleotide repeat expansions.
por: Kim Debacker, et al.
Publicado: (2012) -
Restarted replication forks are error-prone and cause CAG repeat expansions and contractions.
por: Michaela A Gold, et al.
Publicado: (2021) -
Precise CAG repeat contraction in a Huntington’s Disease mouse model is enabled by gene editing with SpCas9-NG
por: Seiya Oura, et al.
Publicado: (2021) -
Quantification of age-dependent somatic CAG repeat instability in Hdh CAG knock-in mice reveals different expansion dynamics in striatum and liver.
por: Jong-Min Lee, et al.
Publicado: (2011) -
Histone deacetylase 10 structure and molecular function as a polyamine deacetylase
por: Yang Hai, et al.
Publicado: (2017)