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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. Among authors: liang b. 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
KCNE3 R53H substitution in familial atrial fibrillation.
Zhang DF, Liang B, Lin J, Liu B, Zhou QS, Yang YQ. Zhang DF, et al. Among authors: liang b. Chin Med J (Engl). 2005 Oct 20;118(20):1735-8. Chin Med J (Engl). 2005. PMID: 16313760 No abstract available.
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.
Common and rare variants in SCN10A modulate the risk of atrial fibrillation.
Jabbari J, Olesen MS, Yuan L, Nielsen JB, Liang B, Macri V, Christophersen IE, Nielsen N, Sajadieh A, Ellinor PT, Grunnet M, Haunsø S, Holst AG, Svendsen JH, Jespersen T. Jabbari J, et al. Among authors: liang b. Circ Cardiovasc Genet. 2015 Feb;8(1):64-73. doi: 10.1161/HCG.0000000000000022. Circ Cardiovasc Genet. 2015. PMID: 25691686 Free PMC article. Clinical Trial.
Mutations in PADI6 Cause Female Infertility Characterized by Early Embryonic Arrest.
Xu Y, Shi Y, Fu J, Yu M, Feng R, Sang Q, Liang B, Chen B, Qu R, Li B, Yan Z, Mao X, Kuang Y, Jin L, He L, Sun X, Wang L. Xu Y, et al. Among authors: liang b. Am J Hum Genet. 2016 Sep 1;99(3):744-752. doi: 10.1016/j.ajhg.2016.06.024. Epub 2016 Aug 18. Am J Hum Genet. 2016. PMID: 27545678 Free PMC article.
4,078 results