Please use this identifier to cite or link to this item: https://doi.org/10.1097/MNH.0b013e3283503068
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dc.titleThe kidney and hypertension: Novel insights from transgenic models
dc.contributor.authorHerrera, M.
dc.contributor.authorCoffman, T.M.
dc.date.accessioned2016-06-01T10:32:50Z
dc.date.available2016-06-01T10:32:50Z
dc.date.issued2012-03
dc.identifier.citationHerrera, M., Coffman, T.M. (2012-03). The kidney and hypertension: Novel insights from transgenic models. Current Opinion in Nephrology and Hypertension 21 (2) : 171-178. ScholarBank@NUS Repository. https://doi.org/10.1097/MNH.0b013e3283503068
dc.identifier.issn10624821
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/124877
dc.description.abstractPurpose of review: Despite decades of study, the pathogenesis of essential hypertension remains obscure, but the kidney appears to play a central role. Technology for manipulation of the mouse genome has been immensely valuable in dissecting pathways involved in blood pressure control. This review summarizes recent studies employing this technology to understand signaling pathways and specific cell lineages within the kidney that are involved in the regulation of sodium excretion impacting blood pressure homeostasis. Recent findings: We review a series of recent studies of regulatory pathways affecting sodium excretion by the kidney including the renin-angiotensin system, the mineralocorticoid receptor, the endothelin system, nitric oxide, and the with-no-lysine (K)/sterile 20-like kinase pathway. We have specifically highlighted studies utilizing transgenic mouse models, which provide a powerful mechanism for defining the role of proteins and pathways on sodium balance and blood pressure in the intact organism. Summary: These studies underscore the importance of the kidney in regulation of blood pressure and the pathogenesis of hypertension. Transgenic mouse models provide a powerful approach to identifying key cell lineages and molecular pathways causing hypertension. These pathways represent potential targets for novel antihypertensive therapies. © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1097/MNH.0b013e3283503068
dc.sourceScopus
dc.subjectangiotensin II
dc.subjecthypertension
dc.subjectkidney
dc.subjectknockout
dc.subjecttransgenic
dc.typeReview
dc.contributor.departmentDUKE-NUS GRADUATE MEDICAL SCHOOL S'PORE
dc.description.doi10.1097/MNH.0b013e3283503068
dc.description.sourcetitleCurrent Opinion in Nephrology and Hypertension
dc.description.volume21
dc.description.issue2
dc.description.page171-178
dc.description.codenCNHYE
dc.identifier.isiut000300406200009
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