Literature DB >> 11530294

The heart SNPs a beat: polymorphisms in candidate genes for cardiovascular disease.

G Q Daley1, M Cargill.   

Abstract

Several environmental risk factors of cardiovascular disease are well established, but genetic risk alleles contributing to the disease in the general population are hotly debated. New strategies focusing on polymorphism discovery in candidate disease genes followed by tests of association to genes across the genome offer a pioneering approach to identifying risk alleles. Several hundred candidate genes for cardiovascular disease have been screened for common polymorphisms and these variants may provide susceptibility alleles which largely contribute to risk of cardiovascular disease in the general population. However, the impact of common susceptibility alleles for disease management will depend on many years of future investigation.

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Year:  2001        PMID: 11530294     DOI: 10.1016/s1050-1738(01)00087-1

Source DB:  PubMed          Journal:  Trends Cardiovasc Med        ISSN: 1050-1738            Impact factor:   6.677


  7 in total

1.  Cardiac channelopathy causing sudden death as revealed by molecular autopsy.

Authors:  Silke Kauferstein; Nadine Kiehne; Steve Peigneur; Jan Tytgat; Hansjürgen Bratzke
Journal:  Int J Legal Med       Date:  2012-02-28       Impact factor: 2.686

2.  Association between SNP rs10569304 on the second expressed region of hole gene and the congenital heart disease.

Authors:  Yali Zhang; Lin Xu; Jian Qiu; Zhiliang Li; Linhai Li; Guangli Ren; Airong Dong; Bingling Li; Mingxiao Ge; Shiren Meng; Jianqing Wang
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2010-08-17

Review 3.  Smoking-gene interaction and disease development: relevance to pancreatic cancer and atherosclerosis.

Authors:  Xing Li Wang; Jian Wang
Journal:  World J Surg       Date:  2005-03       Impact factor: 3.352

4.  High-Risk Polymorphisms Associated with the Molecular Function of Human HMGCR Gene Infer the Inhibition of Cholesterol Biosynthesis.

Authors:  Keshob Chandra Das; Mohammad Uzzal Hossain; Md Moniruzzaman; Md Salimullah; Sharif Akhteruzzaman
Journal:  Biomed Res Int       Date:  2022-06-06       Impact factor: 3.246

5.  Mutation analysis of KCNQ1, KCNH2, SCN5A, KCNE1 and KCNE2 genes in Chinese patients with long QT syndrome.

Authors:  Rong Du; Li Tian; Guohui Yuan; Jin Li; Faxin Ren; Le Gui; Wei Li; Shouyan Zhang; Cailian Kang; Junguo Yang
Journal:  Front Med China       Date:  2007-07-01

6.  A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation.

Authors:  Prakash C Viswanathan; D Woodrow Benson; Jeffrey R Balser
Journal:  J Clin Invest       Date:  2003-02       Impact factor: 14.808

7.  Genetics of Cardiovascular Disease.

Authors:  Ana Stavljenic-Rukavina
Journal:  EJIFCC       Date:  2003-07-03
  7 in total

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