Hypertension in the syndrome of apparent mineralocorticoid excess due to mutation of the 11 beta-hydroxysteroid dehydrogenase type 2 gene
about
Molecular basis for hypertension in the "type II variant" of apparent mineralocorticoid excessA genetic defect resulting in mild low-renin hypertensionSystemic hypertension and glaucoma: mechanisms in common and co-occurrenceApparent mineralocorticoid excess syndrome: an overviewPrimary Aldosteronism: Changing Definitions and New Concepts of Physiology and Pathophysiology Both Inside and Outside the Kidney.In silico structure-function analysis of pathological variation in the HSD11B2 gene sequenceDevelopment and function of the human fetal adrenal cortex: a key component in the feto-placental unit.Laboratory investigation of primary aldosteronism.Hormonal hypertension in children: 11beta-hydroxylase deficiency and apparent mineralocorticoid excess.Matching the right drug to the right patient in essential hypertensionGenetics of hypertension: from experimental animals to humans.Herbal Medicine Containing Licorice May Be Contraindicated for a Patient with an HSD11B2 MutationMeasurement and interpretation of blood pressureLinks between dietary salt intake, renal salt handling, blood pressure, and cardiovascular diseases.Tumor necrosis factor alpha and interleukin 1beta enhance the cortisone/cortisol shuttle.Steroid disorders in children: congenital adrenal hyperplasia and apparent mineralocorticoid excessClinical use of laboratory tests for the identification of secondary forms of arterial hypertension.Carbonyl reductases and pluripotent hydroxysteroid dehydrogenases of the short-chain dehydrogenase/reductase superfamily.11beta-hydroxysteroid dehydrogenase type 1 knockout mice show attenuated glucocorticoid-inducible responses and resist hyperglycemia on obesity or stress.Salt, the kidneys, and arterial hypertension.11β-Hydroxysteroid Dehydrogenase Type II is a Potential Target for Prevention of Colorectal TumorigenesisGlucocorticoids and renal Na+ transport: implications for hypertension and salt sensitivity.Inherited secondary nephrogenic diabetes insipidus: concentrating on humans.Hypercortisolism in obesity-associated hypertension.Functional expression, characterization, and purification of the catalytic domain of human 11-beta -hydroxysteroid dehydrogenase type 1.Primary aldosteronism. Part II. Differential diagnosis of primary hyperaldosteronism and pseudoaldosteronism.The 11 beta-hydroxysteroid dehydrogenase enzymes: perspectives and paradoxes.Distal tubular electrolyte transport during inhibition of renal 11beta-hydroxysteroid dehydrogenase.Expression of 11 beta-hydroxysteroid dehydrogenase in rat osteoblastic cells: pre-receptor regulation of glucocorticoid responses in bone.Apparent mineralocorticoid excess syndrome in a Brazilian boy caused by the homozygous missense mutation p.R186C in the HSD11B2 gene.Urinary cortisol/cortisone ratios in hypertensive and normotensive cats.Increased apical targeting of renal ENaC subunits and decreased expression of 11betaHSD2 in HgCl2-induced nephrotic syndrome in rats.11 beta-hydroxysteroid dehydrogenase (11 beta-HSD-II) activity in human placenta: its relationship to placental weight and birth weight and its possible role in hypertension.Mutations in the 11 beta-hydroxysteroid dehydrogenase type II enzyme associated with hypertension and possibly stillbirth.A novel mutation in HSD11B2 causes apparent mineralocorticoid excess in an Omani kindred.
P2860
Q24539134-1EBBF6AC-6EBC-4D6C-BB05-EBD808DDBA86Q24669744-D8CF84A1-944C-44E9-A207-788B746B6AFAQ24670423-2565AFDC-2AFB-4A92-AEB9-977E48C2118FQ28239329-982281C2-D627-4247-9C45-26EFF54026C1Q30248429-63AE7DD6-F10A-49D4-AAD2-19039ECA5414Q30390640-C2385E82-997A-4514-AC7F-0C64846D60F6Q33738624-10594331-8AC6-4164-BE2B-A7DBEBA9853CQ33868500-2FC63509-B6FD-4E9F-90AB-29C143C7E822Q34128709-AC8815FC-CE5A-46BB-84E0-0A8EFEB94FCDQ34284994-DD5B5F8D-60C5-4441-8FD9-FCC9A1F4653EQ34293919-3C5D5D3E-46E1-476E-91AA-7E027D28A01DQ35106732-CA313128-AC1D-4A58-A555-6384CDC98ECCQ35266321-AC89EDA4-DE70-4F98-AD0E-4AEFBF3E1012Q36079020-EB3D8488-CC40-40AD-8DCF-C2E6B6F42462Q36380398-7DB955B8-EABE-4065-A6B5-A43B33E53FF5Q36556877-9E7AC906-B2F8-4369-A34F-7CEEC378AEAAQ36686822-ED6DA807-3B09-4750-9239-AD378BD712A3Q36761677-7190DB3A-F347-492E-A128-EB768CF818FDQ36833926-4795427F-BC57-4C24-9C3D-507284A49A00Q37070973-1F34579B-AAF0-4ABE-88D5-698C3A1FEC82Q37078077-B6775EAB-E189-421D-9801-77A1C6DCECD0Q37727017-042BAA15-173B-4A0B-9F13-B4820BFB4903Q38077934-D6860C19-ACA3-471F-BCA5-76E5FF6DD8CDQ38209733-9E61D376-D8CC-4DED-A28B-0717D4745A4AQ40714438-DBDA7995-AE5D-43E0-BB48-F1F00607C905Q41104863-159ECDE5-CD0F-4A11-863A-9DD7CA45B6D5Q41273230-397EEF14-D9E1-4836-992A-C984DE4852BFQ43513725-5BA5DE20-31A8-4BC8-B3E5-87763C90AD1EQ43545788-1A90D942-2A4C-4EA4-9CC9-DD2F2BCE9774Q46147309-ADCB917C-FA0A-4C05-A8F8-4E62ACF3E35BQ46212694-A961DF04-C80D-4EFB-93DD-8F6B94ABF08EQ46724562-FD1D09F8-A1B7-4AC0-ABEC-8A1FD3758859Q47217557-0AB44636-6AFF-4FD4-B73C-2B7A2FFB70D4Q47869833-099CBB3F-90DD-4CE9-BCAF-80246D9B5241Q51570218-4615DA19-3BF5-4235-A6CB-EE727621BEC3
P2860
Hypertension in the syndrome of apparent mineralocorticoid excess due to mutation of the 11 beta-hydroxysteroid dehydrogenase type 2 gene
description
1996 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի հունվարին հրատարակված գիտական հոդված
@hy
article publié dans la revue scientifique The Lancet
@fr
artículu científicu espublizáu en 1996
@ast
im Januar 1996 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1996/01/13)
@sk
vědecký článek publikovaný v roce 1996
@cs
wetenschappelijk artikel (gepubliceerd op 1996/01/13)
@nl
наукова стаття, опублікована в січні 1996
@uk
name
Hypertension in the syndrome o ...... roid dehydrogenase type 2 gene
@ast
Hypertension in the syndrome o ...... roid dehydrogenase type 2 gene
@en
Hypertension in the syndrome o ...... roid dehydrogenase type 2 gene
@nl
type
label
Hypertension in the syndrome o ...... roid dehydrogenase type 2 gene
@ast
Hypertension in the syndrome o ...... roid dehydrogenase type 2 gene
@en
Hypertension in the syndrome o ...... roid dehydrogenase type 2 gene
@nl
prefLabel
Hypertension in the syndrome o ...... roid dehydrogenase type 2 gene
@ast
Hypertension in the syndrome o ...... roid dehydrogenase type 2 gene
@en
Hypertension in the syndrome o ...... roid dehydrogenase type 2 gene
@nl
P2093
P1433
P1476
Hypertension in the syndrome o ...... roid dehydrogenase type 2 gene
@en
P2093
A. J. Howie
C. B. Whorwood
D. V. Milford
M. C. Sheppard
P. M. Stewart
Z. S. Krozowski
P356
10.1016/S0140-6736(96)90211-1
P407
P577
1996-01-13T00:00:00Z