Notch Signaling Mediates Astrocyte Abnormality in Spinal Muscular Atrophy Model Systems

Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder characterized by the degeneration of spinal motor neurons and muscle atrophy. The disease is mainly caused by low level of the survival motor neuron (SMN) protein, which is coded by two genes, namely SMN1 and SMN2, but le...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Ohuchi, Kazuki, Funato, Michinori, Yoshino, Yuta, Ando, Shiori, Inagaki, Satoshi, Sato, Arisu, Kawase, Chizuru, Seki, Junko, Saito, Toshio, Nishio, Hisahide, Nakamura, Shinsuke, Shimazawa, Masamitsu, Kaneko, Hideo, Hara, Hideaki
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2019
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6403369/
https://ncbi.nlm.nih.gov/pubmed/30842449
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-39788-w
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados