Cystic fibrosis mutations lead to carboxyl-terminal fragments that highlight an early biogenesis step of the cystic fibrosis transmembrane conductance regulator.

Cystic fibrosis mutations lead to carboxyl-terminal fragments that highlight an early biogenesis step of the cystic fibrosis transmembrane conductance regulator.

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http://www.wikidata.org/entity/Q40886989
Correcting the cystic fibrosis disease mutant, A455E CFTRIn vivo and in vitro ivacaftor response in cystic fibrosis patients with residual CFTR function: N-of-1 studies.Ubiquitin C-terminal hydrolase-L1 protects cystic fibrosis transmembrane conductance regulator from early stages of proteasomal degradation.Hsp70 molecular chaperone facilitates endoplasmic reticulum-associated protein degradation of cystic fibrosis transmembrane conductance regulator in yeast.COOH-terminal truncations promote proteasome-dependent degradation of mature cystic fibrosis transmembrane conductance regulator from post-Golgi compartments.CFTR mutations altering CFTR fragmentation.Missense, nonsense, and neutral mutations define juxtaposed regulatory elements of splicing in cystic fibrosis transmembrane regulator exon 9.
P2860

Cystic fibrosis mutations lead to carboxyl-terminal fragments that highlight an early biogenesis step of the cystic fibrosis transmembrane conductance regulator.

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http://www.wikidata.org/entity/Q40886989
description
2000 nî lūn-bûn
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name
Cystic fibrosis mutations lead ...... embrane conductance regulator.
@en
type
label
Cystic fibrosis mutations lead ...... embrane conductance regulator.
@en
prefLabel
Cystic fibrosis mutations lead ...... embrane conductance regulator.
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698
P921
P356
P1433
P1476
Cystic fibrosis mutations lead ...... embrane conductance regulator.
@en
P2093
P2860
P304
P31
P356
P407
P433
P478
P50
P577
P698
P921