Regulation of CFTR channel gating
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Biochemistry
Reference56 articles.
1. Cystic fibrosis: molecular biology and therapeutic implications
2. Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA
3. Cystic fibrosis: a disease in electrolyte transport
4. The spectrum of cystic fibrosis mutations
5. ABC Transporters: From Microorganisms to Man
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1. Molecular dynamics and functional characterization of I37R-CFTR lasso mutation provide insights into channel gating activity;iScience;2022-01
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3. Pharmacological approaches for targeting cystic fibrosis nonsense mutations;European Journal of Medicinal Chemistry;2020-08
4. Current insights into the role of PKA phosphorylation in CFTR channel activity and the pharmacological rescue of cystic fibrosis disease-causing mutants;Cellular and Molecular Life Sciences;2016-10-08
5. Electrolyte Secretion and Absorption in the Small Intestine and Colon;Yamada' s Textbook of Gastroenterology;2015-11-27
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