(Q28297160)

2

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H Nikkilä

3

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A K Agarwal

4

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P C White

https://scigraph.springernature.com/pub.10.1038/ng0895-394

5

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language of work or name

English

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publication date

August 1995

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published in

Nature Genetics

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volume

10

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issue

4

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page(s)

394-9

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exact match

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cites work

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Structural characterization of normal and mutant human steroid 17 alpha-hydroxylase genes: molecular basis of one example of combined 17 alpha-hydroxylase/17,20 lyase deficiency

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

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Evidence for an unidentified steroid in a child with apparent mineralocorticoid hypertension

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Hypertension in a four-year-old child: gas chromatographic and mass spectrometric evidence for deficient hepatic metabolism of steroids

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Metabolic and Blood Pressure Responses to Hydrocortisone in the Syndrome of Apparent Mineralocorticoid Excess*

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Renal mineralocorticoid receptors and hippocampal corticosterone-binding species have identical intrinsic steroid specificity

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Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor

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Mineralocorticoid action: target tissue specificity is enzyme, not receptor, mediated

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LOCALISATION OF 11β-HYDROXYSTEROID DEHYDROGENASE—TISSUE SPECIFIC PROTECTOR OF THE MINERALOCORTICOID RECEPTOR

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The Syndrome of Apparent Mineralocorticoid Excess: Its Association with 1 lβ –Dehydrogenase and 5β –Reductase Deficiency and Some Consequences for Corticosteroid Metabolism*

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A new form of the syndrome of apparent mineralocorticoid excess

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Congenital 11 beta-hydroxysteroid dehydrogenase deficiency associated with juvenile hypertension: corticosteroid metabolite profiles of four patients and their families

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Corticosteroid 11 beta-dehydrogenase of rat tissues: immunological studies

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Characterization of 11 beta-hydroxysteroid dehydrogenase gene expression: identification of multiple unique forms of messenger ribonucleic acid in the rat kidney

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Human placental 11 beta-hydroxysteroid dehydrogenase: evidence for and partial purification of a distinct NAD-dependent isoform

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Tyr-179 and Lys-183 are essential for enzymatic activity of 11β-hydroxysteroid dehydrogenase

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Three-dimensional structure of holo 3 alpha,20 beta-hydroxysteroid dehydrogenase: a member of a short-chain dehydrogenase family

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Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency

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Studies on Steroid Conjugates: VI. Quantitative Paper Chromatography of Urinary Corticosteroids in Essential Hypertension1

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Evidence of coexisting changes in 11 beta-hydroxysteroid dehydrogenase and 5 beta-reductase activity in subjects with untreated essential hypertension

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Deficient inactivation of cortisol by 11 beta-hydroxysteroid dehydrogenase in essential hypertension

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Glucocorticoid exposure in utero: new model for adult hypertension

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A highly polymorphic locus in human DNA

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An improved method for directly sequencing PCR amplified material using dimethyl sulphoxide

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