A carregar...

Rescue of CFTR NBD2 mutants N1303K and S1235R is influenced by the functioning of the autophagosome

The missing phenylalanine at position 508, located in nucleotide-binding domain (NBD1) of the cystic fibrosis transmembrane regulator (CFTR), is the most common cystic fibrosis mutation. Severe disease-causing mutations also occur in NBD2. To provide information on potential therapeutic strategies f...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:J Cyst Fibros
Main Authors: Liu, Qiangni, Sabirzhanova, Inna, Yanda, Murali K., Bergbower, Emily A.S., Boinot, Clément, Guggino, William B., Cebotaru, Liudmila
Formato: Artigo
Idioma:Inglês
Publicado em: 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6435267/
https://ncbi.nlm.nih.gov/pubmed/29936070
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jcf.2018.05.016
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!