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1
KCNH2 pharmacogenomics summary.
Pharmacogenet Genomics. 2010 Dec;20(12):775-7. doi: 10.1097/FPC.0b013e3283349e9c.
2
Polymorphisms and atrial fibrillation: sorting the wheat from the chaff.
Eur Heart J. 2008 Apr;29(7):843-5. doi: 10.1093/eurheartj/ehn066. Epub 2008 Feb 28.
5
LQT5 masquerading as LQT2: a dominant negative effect of KCNE1-D85N rare polymorphism on KCNH2 current.
Europace. 2011 Oct;13(10):1478-83. doi: 10.1093/europace/eur184. Epub 2011 Jun 28.
6
Congenital long QT syndrome: a case report of LQT2 and LQT13 in a neonate.
Europace. 2014 Dec;16(12):1807. doi: 10.1093/europace/euu299.
9
[A novel mutation of the KCNH2 gene in a family with congenital long QT syndrome].
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Feb;27(1):77-80. doi: 10.3760/cma.j.issn.1003-9406.2010.01.017.
10
Gene symbol: KCNH2.
Hum Genet. 2007 Feb;120(6):911.

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3
Modulating the voltage sensor of a cardiac potassium channel shows antiarrhythmic effects.
Proc Natl Acad Sci U S A. 2021 May 18;118(20). doi: 10.1073/pnas.2024215118.
4
Pharmacogenomic Biomarkers and Their Applications in Psychiatry.
Genes (Basel). 2020 Nov 30;11(12):1445. doi: 10.3390/genes11121445.
5
Transcriptomic variation of pharmacogenes in multiple human tissues and lymphoblastoid cell lines.
Pharmacogenomics J. 2017 Mar;17(2):137-145. doi: 10.1038/tpj.2015.93. Epub 2016 Feb 9.
6
Addressing phenoconversion: the Achilles' heel of personalized medicine.
Br J Clin Pharmacol. 2015 Feb;79(2):222-40. doi: 10.1111/bcp.12441.
9
The importance of being profiled: improving drug candidate safety and efficacy using ion channel profiling.
Front Pharmacol. 2011 Dec 13;2:78. doi: 10.3389/fphar.2011.00078. eCollection 2011.
10
Pharmacogenomics and bioinformatics: PharmGKB.
Pharmacogenomics. 2010 Apr;11(4):501-5. doi: 10.2217/pgs.10.15.

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1
Common variants at ten loci modulate the QT interval duration in the QTSCD Study.
Nat Genet. 2009 Apr;41(4):407-14. doi: 10.1038/ng.362. Epub 2009 Mar 22.
2
Common variants at ten loci influence QT interval duration in the QTGEN Study.
Nat Genet. 2009 Apr;41(4):399-406. doi: 10.1038/ng.364. Epub 2009 Mar 22.
4
Common candidate gene variants are associated with QT interval duration in the general population.
J Intern Med. 2009 Apr;265(4):448-58. doi: 10.1111/j.1365-2796.2008.02026.x. Epub 2009 Oct 25.
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Molecular determinants of hERG channel block by terfenadine and cisapride.
J Pharmacol Sci. 2008 Nov;108(3):301-7. doi: 10.1254/jphs.08102fp. Epub 2008 Nov 6.
6
The human ERG1 channel polymorphism, K897T, creates a phosphorylation site that inhibits channel activity.
Proc Natl Acad Sci U S A. 2008 Sep 23;105(38):14704-8. doi: 10.1073/pnas.0802250105. Epub 2008 Sep 12.
7
Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome.
Heart Rhythm. 2008 Sep;5(9):1275-81. doi: 10.1016/j.hrthm.2008.05.033. Epub 2008 Jun 4.
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hERG potassium channels and the structural basis of drug-induced arrhythmias.
Chem Res Toxicol. 2008 May;21(5):1005-10. doi: 10.1021/tx800035b. Epub 2008 May 1.

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