Literature DB >> 11310586

Multiple single-nucleotide polymorphisms (SNPs) in the Japanese population in six candidate genes for long QT syndrome.

H Iwasa1, M Kurabayashi, R Nagai, Y Nakamura, T Tanaka.   

Abstract

We report here 20 single-nucleotide polymorphisms (SNPs), including 15 novel ones, in six genes that are considered to be candidates for long QT syndrome (LQTS): 2 SNPs in KCNB1, 3 in KCND3, 3 in KCNJ11, 7 in ABCC9, 3 in ADRB1, and 2 in SLC18A2. We also examined their allelic frequencies in a Japanese sample population of LQTS-affected and nonaffected individuals. These data will be useful for genetic association studies designed to investigate acquired arrhythmias.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11310586     DOI: 10.1007/s100380170106

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  6 in total

1.  Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study.

Authors:  Horst Wedekind; Thomas Bajanowski; Patrick Friederich; Günter Breithardt; Thomas Wülfing; Cornelia Siebrands; Birgit Engeland; Gerold Mönnig; Wilhelm Haverkamp; Bernd Brinkmann; Eric Schulze-Bahr
Journal:  Int J Legal Med       Date:  2005-07-13       Impact factor: 2.686

2.  Vmat2 heterozygous mutant mice display a depressive-like phenotype.

Authors:  Masato Fukui; Ramona M Rodriguiz; Jiechun Zhou; Sara X Jiang; Lindsey E Phillips; Marc G Caron; William C Wetsel
Journal:  J Neurosci       Date:  2007-09-26       Impact factor: 6.167

Review 3.  Pharmacogenetic aspects of drug-induced torsade de pointes: potential tool for improving clinical drug development and prescribing.

Authors:  Rashmi R Shah
Journal:  Drug Saf       Date:  2004       Impact factor: 5.606

4.  Association of KCNB1 polymorphisms with lipid metabolisms and insulin resistance: a case-control design of population-based cross-sectional study in Chinese Han population.

Authors:  Yuncui Yu; Jing Wang; Ruiying Kang; Jing Dong; Yuxiang Zhang; Fen Liu; Yuxiang Yan; Rong Zhu; Lili Xia; Xiaoxia Peng; Ling Zhang; Dian He; Herbert Y Gaisano; Gaisano Herbert; Zhenwen Chen; Yan He
Journal:  Lipids Health Dis       Date:  2015-09-17       Impact factor: 3.876

5.  Epilepsy and neurobehavioral abnormalities in mice with a dominant-negative KCNB1 pathogenic variant.

Authors:  Nicole A Hawkins; Sunita N Misra; Manuel Jurado; Seok Kyu Kang; Nicholas C Vierra; Kimberly Nguyen; Lisa Wren; Alfred L George; James S Trimmer; Jennifer A Kearney
Journal:  Neurobiol Dis       Date:  2020-10-22       Impact factor: 5.996

6.  ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology.

Authors:  Peter T Nelson; Steven Estus; Erin L Abner; Ishita Parikh; Manasi Malik; Janna H Neltner; Eseosa Ighodaro; Wang-Xia Wang; Bernard R Wilfred; Li-San Wang; Walter A Kukull; Kannabiran Nandakumar; Mark L Farman; Wayne W Poon; Maria M Corrada; Claudia H Kawas; David H Cribbs; David A Bennett; Julie A Schneider; Eric B Larson; Paul K Crane; Otto Valladares; Frederick A Schmitt; Richard J Kryscio; Gregory A Jicha; Charles D Smith; Stephen W Scheff; Joshua A Sonnen; Jonathan L Haines; Margaret A Pericak-Vance; Richard Mayeux; Lindsay A Farrer; Linda J Van Eldik; Craig Horbinski; Robert C Green; Marla Gearing; Leonard W Poon; Patricia L Kramer; Randall L Woltjer; Thomas J Montine; Amanda B Partch; Alexander J Rajic; KatieRose Richmire; Sarah E Monsell; Gerard D Schellenberg; David W Fardo
Journal:  Acta Neuropathol       Date:  2014-04-27       Impact factor: 15.887

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.