Literature DB >> 18819818

The genetics of cardiovascular disease.

Christian Delles1, Martin W McBride, Sandosh Padmanabhan, Anna F Dominiczak.   

Abstract

Recent advances in genotyping technology and insights into disease mechanisms have increased interest in the genetics of cardiovascular disease. Several candidate genes involved in cardiovascular diseases were identified from studies using animal models, and the translation of these findings to human disease is an exciting challenge. There is a trend towards large-scale genome-wide association studies that are subject to strict quality criteria with regard to both genotyping and phenotyping. Here, we review some of the strategies that have been developed to translate findings from experimental models to human disease and outline the need for optimizing global approaches to analyze such results. Findings from ongoing studies are interpreted in the context of disease pathways instead of the more traditional focus on single genetic variants.

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Year:  2008        PMID: 18819818     DOI: 10.1016/j.tem.2008.07.010

Source DB:  PubMed          Journal:  Trends Endocrinol Metab        ISSN: 1043-2760            Impact factor:   12.015


  5 in total

Review 1.  Opportunities and limitations of genetic analysis of hypertensive rat strains.

Authors:  Juan M Saavedra
Journal:  J Hypertens       Date:  2009-06       Impact factor: 4.844

Review 2.  Genetics of the acute coronary syndrome.

Authors:  Massimo Franchini
Journal:  Ann Transl Med       Date:  2016-05

3.  Ambient pollutants, polymorphisms associated with microRNA processing and adhesion molecules: the Normative Aging Study.

Authors:  Elissa H Wilker; Stacey E Alexeeff; Helen Suh; Pantel S Vokonas; Andrea Baccarelli; Joel Schwartz
Journal:  Environ Health       Date:  2011-05-21       Impact factor: 5.984

4.  Assessment of Cardiovascular Risk Factors Among University Students: The Gender Factor.

Authors:  Mohammad Y Gharaibeh; Karem H Alzoubi; Omar F Khabour; Lubna Tinawi; Rawan Hamad; Esraa F Keewan; Sulaiman K Matarneh; Mahmoud A Alomari
Journal:  Cardiol Res       Date:  2012-07-20

5.  Hypervariable intronic region in NCX1 is enriched in short insertion-deletion polymorphisms and showed association with cardiovascular traits.

Authors:  Katrin Kepp; Elin Org; Siim Sõber; Piret Kelgo; Margus Viigimaa; Gudrun Veldre; Neeme Tõnisson; Peeter Juhanson; Margus Putku; Andreas Kindmark; Viktor Kozich; Maris Laan
Journal:  BMC Med Genet       Date:  2010-01-28       Impact factor: 2.103

  5 in total

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