Gene structure and chromosomal localization of the human HSD11K gene encoding the kidney (type 2) isozyme of 11 beta-hydroxysteroid dehydrogenase
about
Brain mineralocorticoid receptors in cognition and cardiovascular homeostasisApparent mineralocorticoid excess syndrome: an overviewThe genetics of essential hypertension.Steroid disorders in children: congenital adrenal hyperplasia and apparent mineralocorticoid excessEpigenetic regulation of 11 beta-hydroxysteroid dehydrogenase type 2 expression11β-hydroxysteroid dehydrogenases: intracellular gate-keepers of tissue glucocorticoid action.In vivo footprinting of the human 11beta-hydroxysteroid dehydrogenase type 2 promoter: evidence for cell-specific regulation by Sp1 and Sp3.Type 1 11beta -hydroxysteroid dehydrogenase mediates glucocorticoid activation and insulin release in pancreatic islets.Adverse maternal exposures, methylation of glucocorticoid-related genes and perinatal outcomes: a systematic review.Expression of HSD11K (NAD+ dependent 11beta-hydroxysteroid dehydrogenase) promoter constructs in renal cell lines.Hydroxysteroid dehydrogenase HSD1L is localised to the pituitary-gonadal axis of primates.Function, gene organization and protein structures of 11beta-hydroxysteroid dehydrogenase isoforms.Lack of mutations of type 1 11beta-hydroxysteroid dehydrogenase gene in patients with abdominal obesity.Apparent mineralocorticoid excess syndrome in a Brazilian boy caused by the homozygous missense mutation p.R186C in the HSD11B2 gene.11beta-hydroxysteroid dehydrogenase type 2 is the predominant isozyme in the guinea pig placenta: decreases in messenger ribonucleic acid and activity at term.Serum cortisol and cortisone levels in newborns with congenital adrenal hyperplasia before the start of therapy.Proinflammatory cytokines inhibit human placental 11beta-hydroxysteroid dehydrogenase type 2 activity through Ca2+ and cAMP pathways.Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency.Effect of carbenoxolone on the plasma renin activity and hypothalamic-pituitary-adrenal axis in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.Citosine-Adenine-Repeat Microsatellite of 11β-hydroxysteroid dehydrogenase 2 Gene in Hypertensive Children.
P2860
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P2860
Gene structure and chromosomal localization of the human HSD11K gene encoding the kidney (type 2) isozyme of 11 beta-hydroxysteroid dehydrogenase
description
1995 nî lūn-bûn
@nan
1995 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年学术文章
@wuu
1995年学术文章
@zh-cn
1995年学术文章
@zh-hans
1995年学术文章
@zh-my
1995年学术文章
@zh-sg
1995年學術文章
@yue
name
Gene structure and chromosomal ...... a-hydroxysteroid dehydrogenase
@ast
Gene structure and chromosomal ...... a-hydroxysteroid dehydrogenase
@en
Gene structure and chromosomal ...... a-hydroxysteroid dehydrogenase
@nl
type
label
Gene structure and chromosomal ...... a-hydroxysteroid dehydrogenase
@ast
Gene structure and chromosomal ...... a-hydroxysteroid dehydrogenase
@en
Gene structure and chromosomal ...... a-hydroxysteroid dehydrogenase
@nl
prefLabel
Gene structure and chromosomal ...... a-hydroxysteroid dehydrogenase
@ast
Gene structure and chromosomal ...... a-hydroxysteroid dehydrogenase
@en
Gene structure and chromosomal ...... a-hydroxysteroid dehydrogenase
@nl
P2093
P356
P1433
P1476
Gene structure and chromosomal ...... a-hydroxysteroid dehydrogenase
@en
P2093
P356
10.1006/GENO.1995.1231
P407
P577
1995-09-01T00:00:00Z