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

Autor: Gina Picchiarelli, Luc Dupuis

Publikováno v: Cell Stress, Vol 4, Iss 4, Pp 76-91 (2020)

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

Externí odkaz: https://doaj.org/article/072c60ac4c9d47aba661d5b547e13459

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

Autor: Picchiarelli, Gina, Dupuis, Luc

Publikováno v: Cell Stress
Cell Stress, Shared Science Publishers OG, 2020, 4 (4), pp.76-91. ⟨10.15698/cst2020.04.217⟩
Cell Stress, 2020, 4 (4), pp.76-91. ⟨10.15698/cst2020.04.217⟩
Cell Stress, Vol 4, Iss 4, Pp 76-91 (2020)

International audience; 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), includin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::1e7396c6d3e06664a66a1c832369c4e7
https://www.hal.inserm.fr/inserm-03376301/document

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

Autor: Picchiarelli G; Université de Strasbourg, INSERM, Mécanismes Centraux et Périphériques de la Neurodégénérescence, UMR_S 1118, Strasbourg, France., Dupuis L; Université de Strasbourg, INSERM, Mécanismes Centraux et Périphériques de la Neurodégénérescence, UMR_S 1118, Strasbourg, France.

Publikováno v: Cell stress [Cell Stress] 2020 Mar 10; Vol. 4 (4), pp. 76-91. Date of Electronic Publication: 2020 Mar 10.