| 1 | KCNJ11, KCNJ14, KCNJ2, KCNJ4, KCNJ5, kCNJ8
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| Molecular and functional characterization of inwardly rectifying K+ currents in murine proximal colon.2018 Dec 27. PMID:
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| Huang X, Lee SH, Lu H, Sanders KM, Koh SD.
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| J Physiol. Feb 1;596(3):379-391. doi: 10.1113/JP275234. Epub 2017 2018
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| 2 | KCNJ5, LQT13
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| A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1.
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| Kokunai Y, Nakata T, Furuta M, Sakata S, Kimura H, Aiba T, Yoshinaga M, Osaki Y, Nakamori M, Itoh H, Sato T, Kubota T, Kadota K, Shindo K, Mochizuki H, Shimizu W, Horie M, Okamura Y, Ohno K, Takahashi MP.
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| Neurology 82(12):1058-64. doi: 10.1212/WNL.0000000000000239. Epub 2014 Feb 26.
2014
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| 3 | FHA3, KCNJ5
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| A novel Y152C KCNJ5 mutation responsible for familial hyperaldosteronism type III.
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| Monticone S, Hattangady NG, Penton D, Isales C, Edwards MA, Williams TA, Sterner C, Warth R, Mulatero P, Rainey WE.
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| J Clin Endocrinol Metab Clin Endocrinol Metab. 2013 Sep 13. [Epub ahead of print]
2013
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| 4 | KCNJ5
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| Regulation of Aldosterone Biosynthesis by the Kir3.4 (KCNJ5) Potassium Channel.
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| Velarde-Miranda C, Gomez-Sanchez EP, Gomez-Sanchez CE.
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| Clin Exp Pharmacol Physiol lin Exp Pharmacol Physiol. 2013 Jul 5. doi: 10.1111/1440-1681.12151. [Epub ahead of print]
2013
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| 5 | FHA3, KCNJ5
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| Role of KCNJ5 in familial and sporadic primary aldosteronism.
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| Mulatero P, Monticone S, Rainey WE, Veglio F, Williams TA.
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| Nat Rev Endocrinol 9(2):104-12. doi: 10.1038/nrendo.2012.230. Epub 2012 Dec 11. Review.
2013
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| 6 | ATP1A1, CACNA1D, KCNJ5
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| Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension.
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| Azizan EA, Poulsen H, Tuluc P, Zhou J, Clausen MV, Lieb A, Maniero C, Garg S, Bochukova EG, Zhao W, Shaikh LH, Brighton CA, Teo AE, Davenport AP, Dekkers T, Tops B, Küsters B, Ceral J, Yeo GS, Neogi SG, McFarlane I, Rosenfeld N, Marass F, Hadfield J, Margas W, Chaggar K, Solar M, Deinum J, Dolphin AC, Farooqi IS, Striessnig J, Nissen P, Brown MJ.
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| Nat Genet 45(9):1055-60. doi: 10.1038/ng.2716. Epub 2013 Aug 4.
2013
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| 7 | KCNJ5, LQT13
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| The phenotype characteristics of type 13 long QT syndrome with mutation in KCNJ5 (Kir3.4-G387R).
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| Wang F, Liu J, Hong L, Liang B, Graff C, Yang Y, Christiansen M, Olesen SP, Zhang L, Kanters JK.
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| Heart Rhythm 10(10):1500-6. doi: 10.1016/j.hrthm.2013.07.022. Epub 2013 Jul 18.
2013
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| 8 | FHA3, KCNJ5
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| Hypertension with or without adrenal hyperplasia due to different inherited mutations in the potassium channel KCNJ5.
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| Scholl UI, Nelson-Williams C, Yue P, Grekin R, Wyatt RJ, Dillon MJ, Couch R, Hammer LK, Harley FL, Farhi A, Wang WH, Lifton RP.
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| Proc Natl Acad Sci U S A 109(7):2533-8. doi: 10.1073/pnas.1121407109. Epub 2012 Jan 30.
2012
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| 9 | KCNJ5
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| The potassium channel, Kir3.4 participates in angiotensin II-stimulated aldosterone production by a human adrenocortical cell line.
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| Oki K, Plonczynski MW, Lam ML, Gomez-Sanchez EP, Gomez-Sanchez CE.
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| Endocrinology 153(9):4328-35. doi: 10.1210/en.2012-1241. Epub 2012 Jul 13.
2012
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| 10 | KCNJ5
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| G-protein-gated inwardly rectifying K+ channel 4 (GIRK4) immunoreactivity in chemically defined neurons of the hypothalamic arcuate nucleus that control body weight.
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| Kloukina V, Herzer S, Karlsson N, Perez M, Daraio T, Meister B.
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| J Chem Neuroanat 44(1):14-23. doi: 10.1016/j.jchemneu.2012.03.003. Epub 2012 Mar 23.
2012
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| 11 | FHA3, KCNJ3, KCNJ5
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| K+ channel mutations in adrenal aldosterone-producing adenomas and hereditary hypertension.
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| Choi M, Scholl UI, Yue P, Björklund P, Zhao B, Nelson-Williams C, Ji W, Cho Y, Patel A, Men CJ, Lolis E, Wisgerhof MV, Geller DS, Mane S, Hellman P, Westin G, Åkerström G, Wang W, Carling T, Lifton RP.
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| Science 331(6018):768-72.
2011
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| 12 | FHA3, KCNJ5
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| Mutations in KCNJ5 gene cause hyperaldosteronism.
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| Zennaro MC, Jeunemaitre X.
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| Circ Res 108(12):1417-8. Review. No abstract available.
2011
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| 13 | KCNJ5, KCNJ6, KCNJ9
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| Identification of GIRK2-4 subunits in human esophageal smooth muscle cells.
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| Lu Q, Gong L, Xu H, Zhang T, Yan X, Zhao J, Zhang Z, Wang Y, Han Y.
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| Mol Med Rep 4(5):941-5. doi: 10.3892/mmr.2011.499. Epub 2011 May 31.
2011
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| 14 | KCNJ5, LQT13
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| Identification of a Kir3.4 mutation in congenital long QT syndrome.
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| Yang Y, Yang Y, Liang B, Liu J, Li J, Grunnet M, Olesen SP, Rasmussen HB, Ellinor PT, Gao L, Lin X, Li L, Wang L, Xiao J, Liu Y, Liu Y, Zhang S, Liang D, Peng L, Jespersen T, Chen YH.
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| Am J Hum Genet 86(6):872-80.PMID: 20560207 2010
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| 15 | KCNJ3, KCNJ5, KCNJ6, KCNJ9
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| G protein-activated inwardly rectifying potassium channels mediate depotentiation of long-term potentiation.
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| Chung HJ, Ge WP, Qian X, Wiser O, Jan YN, Jan LY.
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| Proc Natl Acad Sci U S A 106(2):635-40. Epub 2008 Dec 31.
2009
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| 16 | KCNJ5
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| The sulfonylurea receptor, an atypical ATP-binding cassette protein, and its regulation of the KATP channel.
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| Burke MA, Mutharasan RK, Ardehali H.
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| Circ Res 102(2):164-76. Review.
2008
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| 17 | KCNJ5
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| KATP channel: relation with cell metabolism and role in the cardiovascular system.
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| Zhuo ML, Huang Y, Liu DP, Liang CC.
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| Int J Biochem Cell Biol 37(4):751-64. Review.
2005
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| 18 | KCNJ3, KCNJ5, KCNJ6
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| Role of G protein-gated inwardly rectifying potassium channels in P2Y12 receptor-mediated platelet functional responses.
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| Shankar H, Murugappan S, Kim S, Jin J, Ding Z, Wickman K, Kunapuli SP.
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| Blood 104(5):1335-43. Epub 2004 May 13.
2004
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| 19 | CLCN6, CLCN7, CLCN8, CLIC1, HTR3B, KCNAB1, KCNB1, KCNJ1, KCNJ2, KCNJ3, KCNJ5, KCNMA1
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| Chromosomal localization of 15 ion channel genes.
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| Russell MWW, et al.
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| Somat Cell Mol Genet 22 : 425-431. 1996
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| 20 | KCNJ5
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| A G-protein-activated inwardly rectifying K+ channel (GIRK4) from human hippocampus associates with other GIRK channels.
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| Spauschus A, Lentes KU, Wischmeyer E, Dissmann E, Karschin C, Karschin A.
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| J Neurosci 16(3):930-8.
1996
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| 21 | KCNJ5
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| Assignment of KATP-1, the cardiac ATP-sensitive potassium channel gene (KCNJ5), to human chromosome 11q24.
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| Tucker SJ, et al.
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| Genomics 28 : 127-128. 1995
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