Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Callum J, Hall"'
Autor:
Graeme W. Carlile, Qi Yang, Elizabeth Matthes, Jie Liao, Véronique Birault, Helen F. Sneddon, Darren L. Poole, Callum J. Hall, John W. Hanrahan, David Y. Thomas
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-19 (2022)
Abstract Most cases of cystic fibrosis (CF) are caused by class 2 mutations in the cystic fibrosis transmembrane regulator (CFTR). These proteins preserve some channel function but are retained in the endoplasmic reticulum (ER). Partial rescue of the
Externí odkaz:
https://doaj.org/article/6c974b2051ad451a915f788a93fa1833
Autor:
Graeme W, Carlile, Qi, Yang, Elizabeth, Matthes, Jie, Liao, Véronique, Birault, Helen F, Sneddon, Darren L, Poole, Callum J, Hall, John W, Hanrahan, David Y, Thomas
Publikováno v:
Scientific reports. 12(1)
Most cases of cystic fibrosis (CF) are caused by class 2 mutations in the cystic fibrosis transmembrane regulator (CFTR). These proteins preserve some channel function but are retained in the endoplasmic reticulum (ER). Partial rescue of the most com
Autor:
Carlile, Graeme W.1,2 (AUTHOR) graeme.carlile@mcgill.ca, Yang, Qi1,2 (AUTHOR), Matthes, Elizabeth3 (AUTHOR), Liao, Jie3 (AUTHOR), Birault, Véronique4 (AUTHOR), Sneddon, Helen F.5 (AUTHOR), Poole, Darren L.6 (AUTHOR), Hall, Callum J.6 (AUTHOR), Hanrahan, John W.3 (AUTHOR), Thomas, David Y.1,2 (AUTHOR)
Publikováno v:
Scientific Reports. 3/17/2022, Vol. 12 Issue 1, p1-19. 19p.