Renal phenotype in mice lacking the Kir5.1 (Kcnj16) K+ channel subunit contrasts with that observed in SeSAME/EAST syndrome.

The heteromeric inwardly rectifying Kir4.1/Kir5.1 K(+) channel underlies the basolateral K(+) conductance in the distal nephron and is extremely sensitive to inhibition by intracellular pH. The functional importance of Kir4.1/Kir5.1 in renal ion transport has recently been highlighted by mutations i...

Full description

Bibliographic Details
Main Authors: Paulais, M, Bloch-Faure, M, Picard, N, Jacques, T, Ramakrishnan, S, Keck, M, Sohet, F, Eladari, D, Houillier, P, Lourdel, S, Teulon, J, Tucker, S
Format: Journal article
Language:English
Published: 2011