Cargando…
A proposed reverse transcription mechanism for (CAG)n and similar expandable repeats that cause neurological and other diseases
The mechanism of (CAG)n repeat generation, and related expandable repeat diseases in non-dividing cells, is currently understood in terms of a DNA template-based DNA repair synthesis process involving hairpin stabilized slippage, local error-prone repair via MutSβ (MSH2–MSH3) hairpin protective stab...
Autores principales: | Franklin, Andrew, Steele, Edward J., Lindley, Robyn A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7044655/ https://www.ncbi.nlm.nih.gov/pubmed/32140575 http://dx.doi.org/10.1016/j.heliyon.2020.e03258 |
Ejemplares similares
-
Inhibition of mutant huntingtin expression by RNA duplex targeting expanded CAG repeats
por: Fiszer, Agnieszka, et al.
Publicado: (2011) -
Inhibiting Expression of Mutant Huntingtin and Ataxin-3 by Targeting Expanded CAG Repeat RNAs
por: Hu, Jiaxin, et al.
Publicado: (2009) -
Minimizing carry-over PCR contamination in expanded CAG/CTG repeat instability applications
por: Aeschbach, Lorène, et al.
Publicado: (2017) -
FAN1 modifies Huntington’s disease progression by stabilizing the expanded HTT CAG repeat
por: Goold, Robert, et al.
Publicado: (2019) -
Expanded CAG/CTG repeats resist gene silencing mediated by targeted epigenome editing
por: Yang, Bin, et al.
Publicado: (2021)