Biochemical and genetic characterization of 11 ??-hydroxysteroid dehydrogenase type 2 in low-renin essential hypertensives-Reference-Cited by-同舟云学术

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Biochemical and genetic characterization of 11 ??-hydroxysteroid dehydrogenase type 2 in low-renin essential hypertensives

Published:2005-01 Issue:1 Volume:23 Page:71-77
ISSN:0263-6352
Container-title:Journal of Hypertension
language:en
Short-container-title:Journal of Hypertension

Author:

Carvajal Cristian A,Romero Dami??n G,Mosso Lorena M,Gonz??lez Alexis A,Campino Carmen,Montero Joaqu??n,Fardella Carlos E

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology,Internal Medicine

Reference38 articles.

1. Human hypertension caused by mutations in the kidney isozyme of 11β–hydroxysteroid dehydrogenase

2. A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension

3. Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2.

4. Liddle's syndrome: Heritable human hypertension caused by mutations in the β subunit of the epithelial sodium channel

5. Hypertension caused by a truncated epithelial sodium channel γ subunit: genetic heterogeneity of Liddle syndrome

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1. Detection of Urinary Exosomal HSD11B2 mRNA Expression: A Useful Novel Tool for the Diagnostic Approach of Dysfunctional 11β-HSD2-Related Hypertension;Frontiers in Endocrinology;2021-08-23

2. The Research Progress of Monogenic Inherited Hypertension;Rare Diseases;2020-03-25

3. Low-Renin Hypertension;Endocrinology and Metabolism Clinics of North America;2019-12

4. Clinical, Biochemical, and Genetic Characteristics of “Nonclassic” Apparent Mineralocorticoid Excess Syndrome;The Journal of Clinical Endocrinology & Metabolism;2018-09-14

5. Unexpected role of the human cytomegalovirus contribute to essential hypertension in the Kazakh Chinese population of Xinjiang;Bioscience Reports;2018-06-27

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