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Molecular genetics of human blood pressure variation
Author(s): Lifton RP
Source: SCIENCE    Volume: 272    Issue: 5262    Pages: 676-680    Published: MAY 3 1996  
Times Cited: 390     References: 75     
Abstract: Hypertension is a common multifactorial vascular disorder of largely unknown cause. Recognition that hypertension is in part genetically determined has motivated studies to identify mutations that confer susceptibility. Thus far, mutations in at least 10 genes have been shown to alter blood pressure; most of these are rare mutations imparting large quantitative effects that either raise or lower blood pressure. These mutations alter blood pressure through a common pathway, changing salt and water reabsorption in the kidney. These findings demonstrate the utility of molecular genetic approaches to the understanding of blood pressure variation and may provide insight into the physiologic mechanisms underlying common forms of hypertension.
Document Type: Article
Language: English
Reprint Address: Lifton, RP (reprint author), YALE UNIV, SCH MED, HOWARD HUGHES MED INST, 295 CONGRESS AVE, NEW HAVEN, CT 06510 USA
Addresses:
1. YALE UNIV, SCH MED, DEPT MED, BOYER CTR MOLEC MED, NEW HAVEN, CT 06510 USA
2. YALE UNIV, SCH MED, DEPT GENET, NEW HAVEN, CT 06510 USA
Publisher: AMER ASSOC ADVANCEMENT SCIENCE, 1200 NEW YORK AVE, NW, WASHINGTON, DC 20005
Subject Category: Multidisciplinary Sciences
IDS Number: UJ051
ISSN: 0036-8075
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