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Two cystic fibrosis transmembrane conductance regulator mutations have different effects on both pulmonary phenotype and regulation of outwardly rectified chloride currents.

Cystic fibrosis (CF), a disorder of electrolyte transport manifest in the lungs, pancreas, sweat duct, and vas deferens, is caused by mutations in the CF transmembrane conductance regulator (CFTR). The CFTR protein has been shown to function as a cAMP-activated chloride channel and also regulates a...

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Wedi'i Gadw mewn:
Cyhoeddwyd yn:Proc Natl Acad Sci U S A
Prif Awduron: Fulmer, S B, Schwiebert, E M, Morales, M M, Guggino, W B, Cutting, G R
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: National Academy of Sciences 1995
Pynciau:
Research Article
Mynediad Ar-lein:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC41423/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7542778/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.92.15.6832
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