Código QR (código de barras bidimensional)

Analysis of translatomic changes in the Ubqln2P497S model of ALS reveals that motor neurons express muscle-associated genes in non-disease states

IntroductionAmyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease characterized by progressively worsening motor symptoms that lead to eventual fatal paralysis. The number of gene mutations associated with ALS have increased dramatically in recent years, suggesting heterogen...

ver descrição completa

Na minha lista:
Principais autores: Wesley M. Stansberry, Natalie C. Fiur, Melissa M. Robins, Brian A. Pierchala
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2024-11-01
coleção:Frontiers in Neurology
Assuntos:
amyotrophic lateral sclerosis
UBQLN2
proteostasis
neuromuscular disease
motor neuron disease
frontotemporal dementia
Acesso em linha:https://www.frontiersin.org/articles/10.3389/fneur.2024.1491415/full
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registros relacionados