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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Acta Neuropathol Commun
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2020
Matèries:
Research
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars