Cystic Fibrosis Transmembrane Conductance Regulator Differentially Regulates Human and Mouse Epithelial Sodium Channels in Xenopus Oocytes
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference34 articles.
1. Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA
2. CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP
3. Aberrant CFTR-dependent HCO-3 transport in mutations associated with cystic fibrosis
4. Cystic Fibrosis Transmembrane Conductance Regulator-dependent Up-regulation of Kir1.1 (ROMK) Renal K+ Channels by the Epithelial Sodium Channel
5. Cystic Fibrosis Transmembrane Conductance Regulator Facilitates ATP Release by Stimulating a Separate ATP Release Channel for Autocrine Control of Cell Volume Regulation
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1. Drosophila melanogaster as an organism model for studying cystic fibrosis and its major associated microbial infections;Infection and Immunity;2023-11-16
2. The Effect of Dynasore Upon the Negative Interaction Between ENaC and CFTR Channels in Xenopus laevis Oocytes;The Journal of Membrane Biology;2022-01-21
3. Downregulation of epithelial sodium channel (ENaC) activity in human airway epithelia after low temperature incubation;BMJ Open Respiratory Research;2021-02
4. ERp29 as a regulator of Insulin biosynthesis;PLOS ONE;2020-05-20
5. Epithelial Ion Channel Folding and ER-Associated Degradation (ERAD);Physiology in Health and Disease;2020
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