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Summary Anatomy Item Literature (1190) Expression Attributions Wiki
XB-ANAT-721

Papers associated with distal (and kcnj16)

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Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness., Schlingmann KP., J Am Soc Nephrol. June 1, 2021; 32 (6): 1498-1512.

KCNJ10 mutations display differential sensitivity to heteromerisation with KCNJ16., Parrock S., Nephron Physiol. January 1, 2013; 123 (3-4): 7-14.          

Kir5.1 underlies long-lived subconductance levels in heteromeric Kir4.1/Kir5.1 channels from Xenopus tropicalis., Shang L., Biochem Biophys Res Commun. October 23, 2009; 388 (3): 501-5.          

Interaction of the Ca2+-sensing receptor with the inwardly rectifying potassium channels Kir4.1 and Kir4.2 results in inhibition of channel function., Huang C., Am J Physiol Renal Physiol. March 1, 2007; 292 (3): F1073-81.

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