High-potency block of Kir4.1 channels by pentamidine: Molecular basis-Reference-Cited by-同舟云学术

High-potency block of Kir4.1 channels by pentamidine: Molecular basis

Published:2017-11 Issue: Volume:815 Page:56-63
ISSN:0014-2999
Container-title:European Journal of Pharmacology
language:en
Short-container-title:European Journal of Pharmacology

Author:

Aréchiga-Figueroa Iván A.,Marmolejo-Murillo Leticia G.,Cui Meng,Delgado-Ramírez Mayra,van der Heyden Marcel A.G.,Sánchez-Chapula José A.,Rodríguez-Menchaca Aldo A.

Funder

SEP-CONACYT

Universidad Autónoma de San Luis Potosí

CONACyT

Publisher

Elsevier BV

Subject

Pharmacology

Reference38 articles.

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2. Association between variation in the human KCNJ10 potassium ion channel gene and seizure susceptibility;Buono;Epilepsy Res.,2004

3. The anti-protozoal drug pentamidine blocks KIR2.x-mediated inward rectifier current by entering the cytoplasmic pore region of the channel;de Boer;Br. J. Pharmacol.,2010

4. Pentamidine isethionate in the treatment of Pneumocystis carinii pneumonia;Drake;Clin. Pharm.,1985

5. Strong voltage-dependent inward rectification of inward rectifier K+ channels is caused by intracellular spermine;Fakler;Cell,1995

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4. VU6036720: The First Potent and Selective In Vitro Inhibitor of Heteromeric Kir4.1/5.1 Inward Rectifier Potassium Channels;Molecular Pharmacology;2022-03-03

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