Molecular Mechanisms of Human Hypertension
Top Cited Papers
- 1 February 2001
- Vol. 104 (4) , 545-556
- https://doi.org/10.1016/s0092-8674(01)00241-0
Abstract
No abstract availableThis publication has 82 references indexed in Scilit:
- Evidence for a Gene Influencing Blood Pressure on Chromosome 17Hypertension, 2000
- Seven Lessons From Two Candidate Genes in Human Essential HypertensionHypertension, 1999
- Role of gammaENaC subunit in lung liquid clearance and electrolyte balance in newborn mice. Insights into perinatal adaptation and pseudohypoaldosteronism.Journal of Clinical Investigation, 1998
- Association of hypertension with T594M mutation in β subunit of epithelial sodium channels in black people resident in LondonThe Lancet, 1998
- Hypertension caused by a truncated epithelial sodium channel γ subunit: genetic heterogeneity of Liddle syndromeNature Genetics, 1995
- Molecular basis of human hypertension: Role of angiotensinogenCell, 1992
- Absence of linkage between the angiotensin converting enzyme locus and human essential hypertensionNature Genetics, 1992
- Congenitally defective aldosterone biosynthesis in humans: The involvement of point mutations of the P-450C18 gene (CYP11B2) in CMO II deficient patientsBiochemical and Biophysical Research Communications, 1992
- Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromesThe Journal of Pediatrics, 1992
- Chromosomal mapping of two genetic loci associated with blood-pressure regulation in hereditary hypertensive ratsNature, 1991