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Summary Anatomy Item Literature (7748) Expression Attributions Wiki
XB-ANAT-11

Papers associated with brain (and kcnj10)

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Developmental gene expression patterns in the brain and liver of Xenopus tropicalis during metamorphosis climax., Yaoita Y., Genes Cells. December 1, 2018; 23 (12): 998-1008.              


Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy., Sicca F., Sci Rep. September 28, 2016; 6 34325.            


TRPV4 and AQP4 Channels Synergistically Regulate Cell Volume and Calcium Homeostasis in Retinal Müller Glia., Jo AO., J Neurosci. September 30, 2015; 35 (39): 13525-37.                  


Contributions of the Na⁺/K⁺-ATPase, NKCC1, and Kir4.1 to hippocampal K⁺ clearance and volume responses., Larsen BR., Glia. April 1, 2014; 62 (4): 608-22.


Generation and validation of a zebrafish model of EAST (epilepsy, ataxia, sensorineural deafness and tubulopathy) syndrome., Mahmood F., Dis Model Mech. May 1, 2013; 6 (3): 652-60.        


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


KCNJ10 mutations disrupt function in patients with EAST syndrome., Freudenthal B., Nephron Physiol. January 1, 2011; 119 (3): p40-8.


Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations., Bockenhauer D., N Engl J Med. May 7, 2009; 360 (19): 1960-70.


H,K-ATPase protein localization and Kir4.1 function reveal concordance of three axes during early determination of left-right asymmetry., Aw S., Mech Dev. January 1, 2008; 125 (3-4): 353-72.    


H bonding at the helix-bundle crossing controls gating in Kir potassium channels., Rapedius M., Neuron. August 16, 2007; 55 (4): 602-14.                


Expression and coexpression of CO2-sensitive Kir channels in brainstem neurons of rats., Wu J., J Membr Biol. February 1, 2004; 197 (3): 179-91.


Modulation of kir4.1 and kir5.1 by hypercapnia and intracellular acidosis., Xu H., J Physiol. May 1, 2000; 524 Pt 3 725-35.


Cloning and characterization of a novel human inwardly rectifying potassium channel predominantly expressed in small intestine., Partiseti M., FEBS Lett. August 28, 1998; 434 (1-2): 171-6.


Cloning and characterization of two K+ inward rectifier (Kir) 1.1 potassium channel homologs from human kidney (Kir1.2 and Kir1.3)., Shuck ME., J Biol Chem. January 3, 1997; 272 (1): 586-93.

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