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Molecular mechanisms of human hypertension

published in: Cell

date of publication: 2001-02-01

language: English

main subject: hypertension

Cites articles 78

Date

Title

Authors

2001-01-01

A novel mouse Nedd4 protein suppresses the activity of the epithelial Na+ channel
2000-03-01

Understanding hypertension through genetic manipulation in mice
2000-06-22

A new locus on chromosome 12p13.3 for pseudohypoaldosteronism type II, an autosomal dominant form of hypertension

Xavier Jeunemaitre
2000-04-01

Salt-sensitive hypertension in endothelin-B receptor-deficient rats
2000-07-07

Activating mineralocorticoid receptor mutation in hypertension exacerbated by pregnancy
2000-06-01

QTL influencing blood pressure maps to the region of PPH1 on chromosome 2q31-34 in Old Order Amish

Braxton D. Mitchell
2000-01-01

Elevated systolic blood pressure as a cardiovascular risk factor
2000-10-01

Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the framingham heart study

L. Adrienne Cupples
2000-05-01

Molecular genetics of human hypertension

Friedrich C. Luft
2000-01-01

eNOS mediates L-arginine-induced inhibition of thick ascending limb chloride flux
2000-01-01

Genetic analysis of inherited hypertension in the rat.
1999-03-01

Defective regulation of the epithelial Na+ channel by Nedd4 in Liddle's syndrome

Hugues Abriel
1999-12-01

Dominant negative mutations in human PPARgamma associated with severe insulin resistance, diabetes mellitus and hypertension

Inês Barroso, John Schwabe, Gareth L. Maslen, Stephen O'Rahilly
1999-06-01

Seven lessons from two candidate genes in human essential hypertension: angiotensinogen and epithelial sodium channel

Pierre Corvol, Alexandre Persu, Xavier Jeunemaitre
1999-07-01

Pulmonary epithelial sodium-channel dysfunction and excess airway liquid in pseudohypoaldosteronism

Aaron Hanukoglu
1999-04-01

Trends in the prevalence of hypertension, antihypertensive therapy, and left ventricular hypertrophy from 1950 to 1989.
1999-02-01

Angiotensinogen gene polymorphisms M235T/T174M: no excess transmission to hypertensive Chinese
1999-01-01

M235T angiotensinogen gene polymorphism and cardiovascular renal risk.

Jan A. Staessen
1998-05-01

Association of hypertension with T594M mutation in beta subunit of epithelial sodium channels in black people resident in London.

Emma H Baker, Pierre Corvol, Xavier Jeunemaitre
1998-10-01

Role of gammaENaC subunit in lung liquid clearance and electrolyte balance in newborn mice. Insights into perinatal adaptation and pseudohypoaldosteronism
1998-05-01

Variation in the region of the angiotensin-converting enzyme gene influences interindividual differences in blood pressure levels in young white males.

Eric Boerwinkle, Sharon L R Kardia, Myriam Fornage
1998-07

Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I
1998-05-01

Evidence for association and genetic linkage of the angiotensin-converting enzyme locus with hypertension and blood pressure in men but not women in the Framingham Heart Study.

Martin G Larson, Richard H Myers
1997-04-17

A clinical trial of the effects of dietary patterns on blood pressure. DASH Collaborative Research Group

Lawrence Appel
1997-04-01

A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro

Xavier Jeunemaitre, John Quackenbush, Jean-Marc Lalouel
1997-06-01

Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21
1997-10-01

The activity of the epithelial sodium channel is regulated by clathrin-mediated endocytosis.
1997-10

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III
1996-03

Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1

Israel Hanukoglu, Aaron Hanukoglu
1996-03-01

Early death due to defective neonatal lung liquid clearance in alpha-ENaC-deficient mice.
1996-05-01

Molecular genetics of human blood pressure variation
1996-09-13

The future of genetic studies of complex human diseases

Article - wd:Q32138445

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