Cargando…
Cockayne Syndrome B protein antagonizes OGG1 in modulating CAG repeat length in vivo
OGG1 and MSH2/MSH3 promote CAG repeat expansion at Huntington's disease (HD) locus in vivo during removal of oxidized bases from DNA. CSB, a transcription-coupled repair (TCR) protein, facilitates repair of some of the same oxidative lesions. In vitro, a knock down CSB results in a reduction of...
Autores principales: | Kovtun, Irina V., Johnson, Kurt O., McMurray, Cynthia T. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3156601/ https://www.ncbi.nlm.nih.gov/pubmed/21566259 |
Ejemplares similares
-
Problems and solutions for the analysis of somatic CAG repeat expansion and their relationship to Huntington's disease toxicity
por: Budworth, Helen, et al.
Publicado: (2016) -
Oxidized dNTPs and the OGG1 and MUTYH DNA glycosylases combine to induce CAG/CTG repeat instability
por: Cilli, Piera, et al.
Publicado: (2016) -
Cockayne syndrome
por: Khan, Firosh, et al.
Publicado: (2008) -
Pseudopapilledema in Cockayne syndrome
por: Brodsky, Michael C., et al.
Publicado: (2021) -
Approaches to Sequence the HTT CAG Repeat Expansion and Quantify Repeat Length Variation
por: Ciosi, Marc, et al.
Publicado: (2021)