Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Clement Boinot"'
Publikováno v:
Cellular Physiology and Biochemistry, Vol 45, Iss 2, Pp 639-655 (2018)
Background/Aims: The CFTR-Associated Ligand (CAL), a PDZ domain containing protein with two coiled-coil domains, reduces cell surface WT CFTR through degradation in the lysosome by a well-characterized mechanism. However, CAL’s regulatory effect on
Externí odkaz:
https://doaj.org/article/04ac1ab1782b4b678f077cdbabf31b2c
Autor:
Emily Anne Smith Bergbower, Inna Sabirzhanova, Clément Boinot, William B. Guggino, Liudmila Cebotaru
Publikováno v:
Cellular Physiology and Biochemistry, Vol 52, Iss 6, Pp 1267-1279 (2019)
Externí odkaz:
https://doaj.org/article/6ad549979b1249a096b4e70ac778cad6
Publikováno v:
Cellular Physiology and Biochemistry, Vol 51, Iss 3, Pp 1489-1499 (2018)
Background/Aims: Cystic fibrosis (CF) is a lethal recessive disorder caused by mutations in the CF transmembrane conductance regulator (CFTR). ΔF508, the most common mutation, is a misfolded protein that is retained in the endoplasmic reticulum and
Externí odkaz:
https://doaj.org/article/72a194b27d754f52b3001997eeaefa36
Publikováno v:
Cellular Physiology and Biochemistry, Vol 41, Iss 6, Pp 2194-2210 (2017)
Background/Aims: Premature degradation of mutated cystic fibrosis transmembrane conductance regulator (CFTR) protein causes cystic fibrosis (CF), the commonest Mendelian disease in Caucasians. Despite recent advances in precision medicines for CF pat
Externí odkaz:
https://doaj.org/article/d1bd1adde0284c35a122fc0d9f0b6a7e