Kir4.2

1

Yuan J et al. Potassium channel KCNJ15 is required for histamine-stimulated gastric acid secretion.
Am. J. Physiol., Cell Physiol., 2015 Aug 15 , 309 (C264-70).

2

Nakajima K et al. KCNJ15/Kir4.2 couples with polyamines to sense weak extracellular electric fields in galvanotaxis.
Nat Commun, 2015 , 6 (8532).

3

Ramos HE et al. Molecular insights into the possible role of Kir4.1 and Kir5.1 in thyroid hormone biosynthesis.
Horm Res Paediatr, 2015 , 83 (141-7).

4

Kumar M et al. Focus on Kir7.1: physiology and channelopathy.
Channels (Austin), 2014 , 8 (488-95).

5

Fukuda H et al. Replication study for the association of a single-nucleotide polymorphism, rs3746876, within KCNJ15, with susceptibility to type 2 diabetes in a Japanese population.
J. Hum. Genet., 2013 Jul , 58 (490-3).

6

Okamoto K et al. Inhibition of glucose-stimulated insulin secretion by KCNJ15, a newly identified susceptibility gene for type 2 diabetes.
Diabetes, 2012 Jul , 61 (1734-41).

7

Veeravalli KK et al. Integrin α9β1-mediated cell migration in glioblastoma via SSAT and Kir4.2 potassium channel pathway.
Cell. Signal., 2012 Jan , 24 (272-81).

8

He W et al. Acid secretion-associated translocation of KCNJ15 in gastric parietal cells.
Am. J. Physiol. Gastrointest. Liver Physiol., 2011 Oct , 301 (G591-600).

9

Edvinsson JM et al. Potassium-dependent activation of Kir4.2 K⁺ channels.
J. Physiol. (Lond.), 2011 Dec 15 , 589 (5949-63).

10

Paynter JJ et al. Random mutagenesis screening indicates the absence of a separate H(+)-sensor in the pH-sensitive Kir channels.
Channels (Austin), 2010 Sep-Oct , 4 (390-7).

11

Summers KM et al. Mutations at KCNQ1 and an unknown locus cause long QT syndrome in a large Australian family: implications for genetic testing.
Am. J. Med. Genet. A, 2010 Mar , 152A (613-21).

12

Okamoto K et al. Identification of KCNJ15 as a susceptibility gene in Asian patients with type 2 diabetes mellitus.
Am. J. Hum. Genet., 2010 Jan , 86 (54-64).

13

Sindić A et al. MUPP1 complexes renal K+ channels to alter cell surface expression and whole cell currents.
Am. J. Physiol. Renal Physiol., 2009 Jul , 297 (F36-45).

14

Yang D et al. Expression of inwardly rectifying potassium channel subunits in native human retinal pigment epithelium.
Exp. Eye Res., 2008 Sep , 87 (176-83).

15

Sun QF et al. Differential gene expression profiles of normal human parotid and submandibular glands.
, 2008 Sep , 14 (500-9).

16

deHart GW et al. The alpha9beta1 integrin enhances cell migration by polyamine-mediated modulation of an inward-rectifier potassium channel.
Proc. Natl. Acad. Sci. U.S.A., 2008 May 20 , 105 (7188-93).

17

Lachheb S et al. Kir4.1/Kir5.1 channel forms the major K+ channel in the basolateral membrane of mouse renal collecting duct principal cells.
Am. J. Physiol. Renal Physiol., 2008 Jun , 294 (F1398-407).

18

Yamamoto Y et al. Expression of inwardly rectifying K+ channels in the carotid body of rat.
Histol. Histopathol., 2008 Jul , 23 (799-806).

19

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

20

Lam HD et al. Modulation of Kir4.2 rectification properties and pHi-sensitive run-down by association with Kir5.1.
Biochim. Biophys. Acta, 2006 Nov , 1758 (1837-45).

21

Pondugula SR et al. Glucocorticoid regulation of genes in the amiloride-sensitive sodium transport pathway by semicircular canal duct epithelium of neonatal rat.
Physiol. Genomics, 2006 Jan 12 , 24 (114-23).

22

Pearson WL et al. C-terminal determinants of Kir4.2 channel expression.
J. Membr. Biol., 2006 , 213 (187-93).

23

Wu JV et al. An inwardly rectifying potassium channel in apical membrane of Calu-3 cells.
J. Biol. Chem., 2004 Nov 5 , 279 (46558-65).

24

Ferrando-Miguel R et al. Protein levels of genes encoded on chromosome 21 in fetal Down Syndrome brain (Part V): overexpression of phosphatidyl-inositol-glycan class P protein (DSCR5).
Amino Acids, 2004 Jun , 26 (255-61).

25

Chen L et al. Inwardly rectifying potassium channels in rat retinal ganglion cells.
Eur. J. Neurosci., 2004 Aug , 20 (956-64).

26

Thiery E et al. Chromosome 21 KIR channels in brain development.
J. Neural Transm. Suppl., 2003 , (105-15).

27

Raap M et al. Diversity of Kir channel subunit mRNA expressed by retinal glial cells of the guinea-pig.
Neuroreport, 2002 Jun 12 , 13 (1037-40).

28

Lourdel S et al. An inward rectifier K(+) channel at the basolateral membrane of the mouse distal convoluted tubule: similarities with Kir4-Kir5.1 heteromeric channels.
J. Physiol. (Lond.), 2002 Jan 15 , 538 (391-404).

29

Hill CE et al. Cloning, expression, and localization of a rat hepatocyte inwardly rectifying potassium channel.
Am. J. Physiol. Gastrointest. Liver Physiol., 2002 Feb , 282 (G233-40).

30

Li Q et al. Models of depressed hepatic mrp2 activity reveal bromosulphophthalein-sensitive passive K+ flux.
Can. J. Physiol. Pharmacol., 2002 Dec , 80 (1167-72).

31

Fujita A et al. Specific localization of an inwardly rectifying K(+) channel, Kir4.1, at the apical membrane of rat gastric parietal cells; its possible involvement in K(+) recycling for the H(+)-K(+)-pump.
J. Physiol. (Lond.), 2002 Apr 1 , 540 (85-92).

32

Pessia M et al. Differential pH sensitivity of Kir4.1 and Kir4.2 potassium channels and their modulation by heteropolymerisation with Kir5.1.
J. Physiol. (Lond.), 2001 Apr 15 , 532 (359-67).

33

Thiery E et al. Developmentally regulated expression of the murine ortholog of the potassium channel KIR4.2 (KCNJ15).
Mech. Dev., 2000 Jul , 95 (313-6).

34

Pearson WL et al. Expression of a functional Kir4 family inward rectifier K+ channel from a gene cloned from mouse liver.
J. Physiol. (Lond.), 1999 Feb 1 , 514 ( Pt 3) (639-53).

35

Kurschner C et al. CIPP, a novel multivalent PDZ domain protein, selectively interacts with Kir4.0 family members, NMDA receptor subunits, neurexins, and neuroligins.
Mol. Cell. Neurosci., 1998 Jun , 11 (161-72).

36

Gosset P et al. A new inward rectifier potassium channel gene (KCNJ15) localized on chromosome 21 in the Down syndrome chromosome region 1 (DCR1).
Genomics, 1997 Sep 1 , 44 (237-41).

37

Ohira M et al. Gene identification in 1.6-Mb region of the Down syndrome region on chromosome 21.
Genome Res., 1997 Jan , 7 (47-58).