Locating a Plausible Binding Site for an Open-Channel Blocker, GlyH-101, in the Pore of the Cystic Fibrosis Transmembrane Conductance Regulator-Reference-Cited by-同舟云学术

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Locating a Plausible Binding Site for an Open-Channel Blocker, GlyH-101, in the Pore of the Cystic Fibrosis Transmembrane Conductance Regulator

Published:2012-08-24 Issue:6 Volume:82 Page:1042-1055
ISSN:0026-895X
Container-title:Molecular Pharmacology
language:en
Short-container-title:Mol Pharmacol

Author:

Norimatsu Yohei,Ivetac Anthony,Alexander Christopher,O'Donnell Nicolette,Frye Leah,Sansom Mark S. P.,Dawson David C.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference60 articles.

1. Cystic Fibrosis Transmembrane Conductance Regulator: Using Differential Reactivity toward Channel-Permeant and Channel-Impermeant Thiol-Reactive Probes To Test a Molecular Model for the Pore

2. Dual roles of the sixth transmembrane segment of the CFTR chloride channel in gating and permeation

3. Conformational Changes in a Pore-lining Helix Coupled to Cystic Fibrosis Transmembrane Conductance Regulator Channel Gating

4. CFTR Gating I

5. Airway Surface Dehydration in Cystic Fibrosis: Pathogenesis and Therapy

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