Molecular mechanism of a COOH‐terminal gating determinant in the ROMK channel revealed by a Bartter's disease mutation
Author:
Affiliation:
1. Department of Physiology, University of Maryland School of Medicine, Baltimore, MD 21201
2. Department of Physiology & Biophysics, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA
Publisher
Wiley
Subject
Physiology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1113/jphysiol.2002.027581
Reference56 articles.
1. Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis
2. Involvement of Histidine Residues in Proton Sensing of ROMK1 Channel
3. A conserved cytoplasmic region of ROMK modulates pH sensitivity, conductance, and gating
4. Mutations in the ROMK Gene in Antenatal Bartter Syndrome Are Associated with Impaired K+Channel Function
5. A Hyperprostaglandin E Syndrome Mutation in Kir1.1 (Renal Outer Medullary Potassium) Channels Reveals a Crucial Residue for Channel Function in Kir1.3 Channels
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