Literature DB >> 9886870

Genetics of experimental hypertension.

A F Dominiczak1, J S Clark, B Jeffs, N H Anderson, C D Negrin, W K Lee, M J Brosnan.   

Abstract

Experimental models of genetic hypertension are used to develop paradigms to study human essential hypertension while removing some of the complexity inherent in the study of human subjects. Since 1991 several quantitative trait loci responsible for blood pressure regulation have been identified in various rat crosses. More recently, a series of interesting quantitative trait loci influencing cardiac hypertrophy, stroke, metabolic syndrome and renal damage has also been described. It is recognized that the identification of large chromosomal regions containing a quantitative trait locus is only a first step towards gene identification. The next step is the production of congenic strains and substrains to confirm the existence of the quantitative trait locus and to narrow down the chromosomal region of interest. Several congenic strains have already been produced, with further refinement of the methodology currently in progress. The ultimate goal is to achieve positional cloning of the causal gene, a task which has so far been elusive. There are several areas of cross-fertilization between experimental and human genetics of hypertension, with a successful transfer of two loci directly from rats to humans and with new pharmacogenetic approaches which may be utilized in both experimental and clinical settings.

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Year:  1998        PMID: 9886870     DOI: 10.1097/00004872-199816121-00003

Source DB:  PubMed          Journal:  J Hypertens        ISSN: 0263-6352            Impact factor:   4.844


  6 in total

Review 1.  Functional genomics in rodent models of hypertension.

Authors:  Martin W McBride; Fadi J Charchar; Delyth Graham; William H Miller; Pamela Strahorn; Fiona J Carr; Anna F Dominiczak
Journal:  J Physiol       Date:  2004-01-01       Impact factor: 5.182

Review 2.  The genomics of cardiovascular disorders: therapeutic implications.

Authors:  P Ferrari; G Bianchi
Journal:  Drugs       Date:  2000-05       Impact factor: 9.546

3.  Substrain differences, gender, and age of spontaneously hypertensive rats critically determine infarct size produced by distal middle cerebral artery occlusion.

Authors:  Hitonori Takaba; Kenji Fukuda; Hiroshi Yao
Journal:  Cell Mol Neurobiol       Date:  2004-10       Impact factor: 5.046

4.  Novel genes on rat chromosome 10 are linked to body fat mass, preadipocyte number and adipocyte size.

Authors:  A Weingarten; L Turchetti; K Krohn; I Klöting; M Kern; P Kovacs; M Stumvoll; M Blüher; N Klöting
Journal:  Int J Obes (Lond)       Date:  2016-07-27       Impact factor: 5.095

Review 5.  Hypertensive renal damage: insights from animal models and clinical relevance.

Authors:  Karen A Griffin; Anil K Bidani
Journal:  Curr Hypertens Rep       Date:  2004-04       Impact factor: 5.369

6.  Deficiency in Six2 during prenatal development is associated with reduced nephron number, chronic renal failure, and hypertension in Br/+ adult mice.

Authors:  Ben Fogelgren; Shiming Yang; Ian C Sharp; Odaro J Huckstep; Wenbin Ma; S J Somponpun; Edward C Carlson; Catherine F T Uyehara; Scott Lozanoff
Journal:  Am J Physiol Renal Physiol       Date:  2009-02-04
  6 in total

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