Genetic disorders of transporters/channels in the inner ear and their relation to the kidney

Pediatric Nephrology : Journal of the International Pediatric Nephrology Association
Theo A PetersJo H A J Curfs

Abstract

Inner ear physiology is reviewed with emphasis on features common to renal physiology. Genetic disorders in transporters/channels for chloride (ClC-K), bicarbonate (Cl(-)/HCO(3)(-) exchanger), protons (H(+)-ATPase), sodium (ENaC, NKKC1, NBC3, NHE3), potassium (KCNQ1/KCNE1, Kcc4), and water (AQP4) in the inner ear and their relation to the kidney are discussed. Based on data from human disorders (with or without mouse counterparts) and mouse models (without human counterparts) this article focuses on the involvement of these transporters/channels in hearing loss.

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Citations

Jul 30, 2009·Pediatric Nephrology : Journal of the International Pediatric Nephrology Association·Elena AndreucciIvana Pela
Jul 10, 2008·Biochemistry·Congbao KangCharles R Sanders
Aug 17, 2005·Audiology & Neuro-otology·Joseph P RochePaul Popper
Dec 26, 2009·Paediatric Drugs·Kristine S SchonderRobert J Weber
Nov 15, 2007·Biochemistry·Jarrod A SmithCharles R Sanders
Aug 19, 2015·Neurosurgical Review·David Satzer, Daniel J Guillaume
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Sep 2, 2008·Drug Safety : an International Journal of Medical Toxicology and Drug Experience·Bertha Maria VerdelAntoine C G Egberts
May 13, 2019·World Journal of Pediatrics : WJP·Sílvia Bouissou Morais SoaresAna Cristina Simões E Silva
Oct 12, 2020·Biochemical Pharmacology·Bianca N QuadeRossana Occhipinti

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