Separation of drug transport and chloride channel functions of the human multidrug resistance P-glycoprotein-Reference-Cited by-同舟云学术

Separation of drug transport and chloride channel functions of the human multidrug resistance P-glycoprotein

Published:1992-10 Issue:1 Volume:71 Page:23-32
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Gill Deborah R.,Hyde Stephen C.,Higgins Christopher F.,Valverde Miguel A.,Mintenig Gerard M.,Sepúlveda Francisco V.

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference55 articles.

1. Demonstration that CFTR is a chloride channel by alteration of its anion selectivity;Anderson;Science,1991

2. Nucleotide triphosphates are required to open the CFTR channel;Anderson;Cell,1991

3. The gene encoding multidrug resistance is induced and expressed at high levels during pregnancy in the secretory epithelium of the uterus;Arceci,1988

4. ATP-sensitive K+ channels in rat pancreatic β-cells: modulation by ATP and Mg2+ ions;Ashcroft;J. Physiol.,1989

5. Discrete mutations introduced in the predicted nucleotide-binding sites of the mdr-1 gene abolish its ability to confer multidrug resistance;Azzaria;Mol. Cell. Biol.,1989

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