RNA dependent suppression of C9orf72 ALS/FTD associated neurodegeneration by Matrin-3

The most common genetic cause of amyotrophic lateral sclerosis (ALS) is a GGGGCC (G4C2) hexanucleotide repeat expansions in first intron of the C9orf72 gene. The accumulation of repetitive RNA sequences can mediate toxicity potentially through the formation of intranuclear RNA foci that sequester ke...

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Detalhes bibliográficos
Publicado no:Acta Neuropathol Commun
Main Authors: Ramesh, Nandini, Daley, Elizabeth L., Gleixner, Amanda M., Mann, Jacob R., Kour, Sukhleen, Mawrie, Darilang, Anderson, Eric N., Kofler, Julia, Donnelly, Christopher J., Kiskinis, Evangelos, Pandey, Udai Bhan
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2020
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7603783/
https://ncbi.nlm.nih.gov/pubmed/33129345
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40478-020-01060-y
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