Literature DB >> 10406815

Evidence for linkage between essential hypertension and a putative locus on human chromosome 17.

J Baima1, M Nicolaou, F Schwartz, A L DeStefano, A Manolis, I Gavras, C Laffer, F Elijovich, L Farrer, C T Baldwin, H Gavras.   

Abstract

Several clinical and animal studies indicate that essential hypertension is inherited as a multifactorial trait with a significant genetic and environmental component. In the stroke-prone spontaneously hypertensive rat model, investigators have found evidence for linkage to blood pressure regulatory genes (quantitative trait loci) on rat chromosomes 2, 10, and X. In 1 human study of French and UK sib pairs, evidence for linkage has been reported to human chromosome 17q, the syntenic region of the rat chromosome 10 quantitative trait loci (QTL). Our study confirms this linkage (P=0.0005) and refines the location of the blood pressure QTL.

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Year:  1999        PMID: 10406815     DOI: 10.1161/01.hyp.34.1.4

Source DB:  PubMed          Journal:  Hypertension        ISSN: 0194-911X            Impact factor:   10.190


  13 in total

Review 1.  Genetic rat models of hypertension: relationship to human hypertension.

Authors:  M Stoll; H J Jacob
Journal:  Curr Hypertens Rep       Date:  2001-04       Impact factor: 5.369

2.  Mapping quantitative trait loci using the MCMC procedure in SAS.

Authors:  S Xu; Z Hu
Journal:  Heredity (Edinb)       Date:  2010-06-16       Impact factor: 3.821

3.  Critique of "chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension" by Rutherford et al., Human Genetics, published online September 2001.

Authors:  Brian J Morris
Journal:  Hum Genet       Date:  2001-12-13       Impact factor: 4.132

Review 4.  The WNKs: atypical protein kinases with pleiotropic actions.

Authors:  James A McCormick; David H Ellison
Journal:  Physiol Rev       Date:  2011-01       Impact factor: 37.312

5.  GOSR2 Lys67Arg is associated with hypertension in whites.

Authors:  Tamra E Meyer; Dov Shiffman; Alanna C Morrison; Charles M Rowland; Judy Z Louie; Lance A Bare; David A Ross; Andre R Arellano; Daniel I Chasman; Paul M Ridker; James S Pankow; Josef Coresh; Mary J Malloy; John P Kane; Stephen G Ellis; James J Devlin; Eric Boerwinkle
Journal:  Am J Hypertens       Date:  2008-12-04       Impact factor: 2.689

6.  Genetic variation and atherosclerosis.

Authors:  Erik Biros; Mirko Karan; Jonathan Golledge
Journal:  Curr Genomics       Date:  2008-03       Impact factor: 2.236

7.  Hypertension and albuminuria in chronic kidney disease mapped to a mouse chromosome 11 locus.

Authors:  H R Salzler; R Griffiths; P Ruiz; L Chi; C Frey; D A Marchuk; H A Rockman; T H Le
Journal:  Kidney Int       Date:  2007-09-12       Impact factor: 10.612

8.  Association of Ala589Ser polymorphism of WNK4 gene with essential hypertension in a high-risk Chinese population.

Authors:  Zhi-Jun Sun; Yan Li; Jing-Yu Lu; Qian Ding; Yu Liang; Jing-Pu Shi; Jesse Li-Ling; Yan-Yan Zhao
Journal:  J Physiol Sci       Date:  2008-12-17       Impact factor: 2.781

9.  Identification of 108 SNPs in TSC, WNK1, and WNK4 and their association with hypertension in a Japanese general population.

Authors:  Yoshihiro Kokubo; Kei Kamide; Nozomu Inamoto; Chihiro Tanaka; Mariko Banno; Shin Takiuchi; Yuhei Kawano; Hitonobu Tomoike; Toshiyuki Miyata
Journal:  J Hum Genet       Date:  2004-08-11       Impact factor: 3.172

10.  An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP).

Authors:  C Charles Gu; Steven C Hunt; Sharon Kardia; Stephen T Turner; Aravinda Chakravarti; Nicholas Schork; Richard Olshen; David Curb; Cashell Jaquish; Eric Boerwinkle; D C Rao
Journal:  Hum Genet       Date:  2007-03-20       Impact factor: 5.881

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