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GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy.
Li RG, Li L, Qiu XB, Yuan F, Xu L, Li X, Xu YJ, Jiang WF, Jiang JQ, Liu X, Fang WY, Zhang M, Peng LY, Qu XK, Yang YQ. Li RG, et al. Among authors: yang yq. Biochem Biophys Res Commun. 2013 Oct 4;439(4):591-6. doi: 10.1016/j.bbrc.2013.09.023. Epub 2013 Sep 13. Biochem Biophys Res Commun. 2013. PMID: 24041700 Free article.
A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation.
Xia M, Jin Q, Bendahhou S, He Y, Larroque MM, Chen Y, Zhou Q, Yang Y, Liu Y, Liu B, Zhu Q, Zhou Y, Lin J, Liang B, Li L, Dong X, Pan Z, Wang R, Wan H, Qiu W, Xu W, Eurlings P, Barhanin J, Chen Y. Xia M, et al. Biochem Biophys Res Commun. 2005 Jul 15;332(4):1012-9. doi: 10.1016/j.bbrc.2005.05.054. Biochem Biophys Res Commun. 2005. PMID: 15922306
Stretch-induced alterations of human Kir2.1 channel currents.
He Y, Xiao J, Yang Y, Zhou Q, Zhang Z, Pan Q, Liu Y, Chen Y. He Y, et al. Biochem Biophys Res Commun. 2006 Dec 15;351(2):462-7. doi: 10.1016/j.bbrc.2006.10.049. Epub 2006 Oct 17. Biochem Biophys Res Commun. 2006. PMID: 17067550
Human KCNQ1 S140G mutation is associated with atrioventricular blocks.
Yang Y, Liu Y, Dong X, Kuang Y, Lin J, Su X, Peng L, Jin Q, He Y, Liu B, Pan Z, Li L, Zhu Q, Lin X, Zhou Q, Pan Q, Eurlings PM, Fei J, Wang Z, Chen YH. Yang Y, et al. Heart Rhythm. 2007 May;4(5):611-8. doi: 10.1016/j.hrthm.2007.01.029. Epub 2007 Feb 1. Heart Rhythm. 2007. PMID: 17467630
Identification of a Kir3.4 mutation in congenital long QT syndrome.
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. Yang Y, et al. Am J Hum Genet. 2010 Jun 11;86(6):872-80. doi: 10.1016/j.ajhg.2010.04.017. Am J Hum Genet. 2010. PMID: 20560207 Free PMC article.
799 results