PubMed for id: 3764

Year	Number of Results
1993	2
1995	2
1997	1
1998	1
1999	2
2000	1
2001	2
2002	6
2003	3
2004	1
2005	3
2006	3
2008	4
2009	4
2010	5
2011	4
2012	5
2013	2
2014	3
2015	1
2017	2
2019	1
2020	4
2021	3
2022	1
2024	0

1

A novel mutation in the KCNJ8 gene encoding the Kir6.1 subunit of an ATP-sensitive potassium channel in a Japanese patient with Cantú syndrome.

Chihara M, Asahina A, Itoh M. Chihara M, et al. J Eur Acad Dermatol Venereol. 2020 Sep;34(9):e476-e478. doi: 10.1111/jdv.16384. Epub 2020 May 6. J Eur Acad Dermatol Venereol. 2020. PMID: 32215968 No abstract available.

2

Cantú syndrome resulting from activating mutation in the KCNJ8 gene.

Cooper PE, Reutter H, Woelfle J, Engels H, Grange DK, van Haaften G, van Bon BW, Hoischen A, Nichols CG. Cooper PE, et al. Hum Mutat. 2014 Jul;35(7):809-13. doi: 10.1002/humu.22555. Epub 2014 May 6. Hum Mutat. 2014. PMID: 24700710 Free PMC article.

3

The KCNJ8-S422L variant previously associated with J-wave syndromes is found at an increased frequency in Ashkenazi Jews.

Veeramah KR, Karafet TM, Wolf D, Samson RA, Hammer MF. Veeramah KR, et al. Eur J Hum Genet. 2014 Jan;22(1):94-8. doi: 10.1038/ejhg.2013.78. Epub 2013 May 1. Eur J Hum Genet. 2014. PMID: 23632791 Free PMC article.

4

KATP channels are up-regulated with increasing age in human myometrium.

Du Q, Jovanović S, Tulić L, Sljivančanin D, Jack DW, Zižić V, Abdul KS, Tulić I, Jovanović A. Du Q, et al. Mech Ageing Dev. 2013 Mar;134(3-4):98-102. doi: 10.1016/j.mad.2013.01.003. Epub 2013 Jan 28. Mech Ageing Dev. 2013. PMID: 23369859

5

A KCNJ8 mutation associated with early repolarization and atrial fibrillation.

Delaney JT, Muhammad R, Blair MA, Kor K, Fish FA, Roden DM, Darbar D. Delaney JT, et al. Europace. 2012 Oct;14(10):1428-32. doi: 10.1093/europace/eus150. Epub 2012 May 4. Europace. 2012. PMID: 22562657 Free PMC article.

6

Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8.

Barajas-Martínez H, Hu D, Ferrer T, Onetti CG, Wu Y, Burashnikov E, Boyle M, Surman T, Urrutia J, Veltmann C, Schimpf R, Borggrefe M, Wolpert C, Ibrahim BB, Sánchez-Chapula JA, Winters S, Haïssaguerre M, Antzelevitch C. Barajas-Martínez H, et al. Heart Rhythm. 2012 Apr;9(4):548-55. doi: 10.1016/j.hrthm.2011.10.035. Epub 2011 Nov 3. Heart Rhythm. 2012. PMID: 22056721 Free PMC article.

7

Loss-of-function mutations in the KCNJ8-encoded Kir6.1 K(ATP) channel and sudden infant death syndrome.

Tester DJ, Tan BH, Medeiros-Domingo A, Song C, Makielski JC, Ackerman MJ. Tester DJ, et al. Circ Cardiovasc Genet. 2011 Oct;4(5):510-5. doi: 10.1161/CIRCGENETICS.111.960195. Epub 2011 Aug 11. Circ Cardiovasc Genet. 2011. PMID: 21836131 Free PMC article.

8

Mutational analysis of Kir6.1 in Japanese patients with coronary spastic angina.

Tomita H, Sasaki S, Osanai T, Nakano T, Higuma T, Yokoyama J, Hanada H, Yasujima M, Okumura K. Tomita H, et al. Int J Mol Med. 2006 Oct;18(4):589-91. Int J Mol Med. 2006. PMID: 16964409

9

Mediation of the effect of nicotine on Kir6.1 channels by superoxide anion production.

Hanna ST, Cao K, Sun X, Wang R. Hanna ST, et al. J Cardiovasc Pharmacol. 2005 May;45(5):447-55. doi: 10.1097/01.fjc.0000159046.35241.4e. J Cardiovasc Pharmacol. 2005. PMID: 15821440

10

Protein kinase G activates inwardly rectifying K(+) channel in cultured human proximal tubule cells.

Nakamura K, Hirano J, Itazawa S, Kubokawa M. Nakamura K, et al. Am J Physiol Renal Physiol. 2002 Oct;283(4):F784-91. doi: 10.1152/ajprenal.00023.2002. Am J Physiol Renal Physiol. 2002. PMID: 12217870 Free article.

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