Role of RNA Binding Proteins with prion-like domains in muscle and neuromuscular diseases

Role of RNA Binding Proteins with prion-like domains in muscle and neuromuscular diseases

A number of neuromuscular and muscular diseases, including amyotrophic lateral sclerosis (ALS), spinal muscular atrophy (SMA) and several myopathies, are associated to mutations in related RNA-binding proteins (RBPs), including TDP-43, FUS, MATR3 or hnRNPA1/B2. These proteins harbor similar modular...

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Bibliographic Details
Main Authors: Gina Picchiarelli, Luc Dupuis
Format: Article
Language:English
Published: Shared Science Publishers OG 2020-03-01
Series:Cell Stress
Subjects:
rna-binding protein (rbp)
muscle
dystrophy
amyotrophic lateral sclerosis (als)
spinal muscular atrophy (sma)
inclusion body myopathy (ibm)
fragile x-associated tremor / ataxia syndrome (fxtas)
multisystem proteinopathy (msp)
huntington’s disease
Online Access:http://www.cell-stress.com/researcharticles/2020a-picchiarelli-cell-stress/

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