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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. Among authors: liang b, liang d. 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.
KCNQ1 loss-of-function mutation impairs gastric acid secretion in mice.
Pan Q, Ma J, Zhou Q, Li J, Tang Y, Liu Y, Yang Y, Xiao J, Peng L, Li P, Liang D, Zhang H, Chen YH. Pan Q, et al. Among authors: liang d. Mol Biol Rep. 2010 Mar;37(3):1329-33. doi: 10.1007/s11033-009-9511-9. Epub 2009 Mar 21. Mol Biol Rep. 2010. PMID: 19306073
Inhibition of mitochondrial translocator protein prevents atrial fibrillation.
Li J, Xiao J, Liang D, Zhang H, Zhang G, Liu Y, Zhang Y, Liu Y, Yu Z, Yan B, Jiang B, Li F, Peng L, Zhou ZN, Chen YH. Li J, et al. Among authors: liang d. Eur J Pharmacol. 2010 Apr 25;632(1-3):60-4. doi: 10.1016/j.ejphar.2010.01.014. Epub 2010 Feb 1. Eur J Pharmacol. 2010. PMID: 20123099
4,730 results