Steroid 11 beta-hydroxylase deficiency and related disorders (Q34246288)

31 July 2017

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title

Steroid 11 beta-hydroxylase deficiency and related disorders. (English)

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31 July 2017

White PC

1

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31 July 2017

publication date

1 March 2001

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Endocrinology and Metabolism Clinics of North America

31 July 2017

published in

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31 July 2017

volume

30

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31 July 2017

issue

1

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31 July 2017

page(s)

61-79, vi

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11 beta-hydroxylase deficiency in hyperandrogenism

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Prenatal diagnosis and treatment of 11beta-hydroxylase deficiency congenital adrenal hyperplasia resulting in normal female genitalia

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Mutations in the CYP11B1 gene causing congenital adrenal hyperplasia and hypertension cluster in exons 6, 7, and 8

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

The Product of the CYP11B2 Gene Is Required for Aldosterone Biosynthesis in the Human Adrenal Cortex

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Differential regulation of 11 beta-hydroxylase and aldosterone synthase in human adrenocortical H295R cells

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Glucocorticoid-remediable aldosteronism (GRA): diagnosis, variability of phenotype and regulation of potassium homeostasis

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Different isozymes of mouse 11 beta-hydroxylase produce mineralocorticoids and glucocorticoids

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Primary aldosteronism: hypertension with a genetic basis

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

19-Nor-Deoxycorticosterone Excretion in Primary Aldosteronism and Low Renin Hypertension*

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Hypertensive potency of 18-oxocortisol in the rat

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Frame shift by insertion of 2 basepairs in codon 394 of CYP11B1 causes congenital adrenal hyperplasia due to steroid 11 beta-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Glucocorticoid-suppressible hyperaldosteronism: effects of crossover site and parental origin of chimaeric gene on phenotypic expression

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

CYP11B1 mutations causing non-classic adrenal hyperplasia due to 11 beta-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

A new genetic test for familial hyperaldosteronism type I aids in the detection of curable hypertension

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Cloning and expression of a cDNA for human cytochrome P-450aldo as related to primary aldosteronism

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Role of steroid 11 beta-hydroxylase and steroid 18-hydroxylase in the biosynthesis of glucocorticoids and mineralocorticoids in humans

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthase

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Hypertension in a neonate with 11 beta-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Congenitally defective aldosterone biosynthesis in humans: inactivation of the P-450C18 gene (CYP11B2) due to nucleotide deletion in CMO I deficient patients

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

The cloning of a family of genes that encode the melanocortin receptors

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Therapeutic effect of calcium channel blockade in primary aldosteronism

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

A nonsense mutation (TGG [Trp116]-->TAG [Stop]) in CYP11B1 causes steroid 11 beta-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

The P450 superfamily: update on new sequences, gene mapping, accession numbers, early trivial names of enzymes, and nomenclature

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Adrenal glomerulosa function in patients with dexamethasone-suppressible hyperaldosteronism

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Production of 19-oic-11-deoxycorticosterone from 19-oxo-11-deoxycorticosterone by cytochrome P-450(11)beta and nonenzymatic production of 19-nor-11-deoxycorticosterone from 19-oic-11-deoxycorticosterone

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Hormonal Studies in Obligate Heterozygotes and Siblings of Patients with l1/?-Hydroxylase Deficiency Congenital Adrenal Hyperplasia*

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Mutations in the human CYP11B2 (aldosterone synthase) gene causing corticosterone methyloxidase II deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Glucocorticoid-suppressible hyperaldosteronism and adrenal tumors occurring in a single French pedigree

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

2 Modeling of mammalian P450s on basis of P450cam x-ray structure

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Crystal structure of hemoprotein domain of P450BM-3, a prototype for microsomal P450's

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Glucocorticoid-remediable aldosteronism in a large kindred: clinical spectrum and diagnosis using a characteristic biochemical phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

The natural history of salt-wasting disorders of adrenal and renal origin

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

High frequency of congenital adrenal hyperplasia (classic 11 beta-hydroxylase deficiency) among Jews from Morocco

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Prenatal Diagnosis of llβ-Hydroxyiase Deficiency Congenital Adrenal Hyperplasia*

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Human CYP11B2 (Aldosterone Synthase) Maps To Chromosome 8q24.3

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Diagnosis and nomenclature of the disorders of the terminal portion of the aldosterone biosynthetic pathway

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Isolated Aldosterone Deficiency in Man: Acquired and Inborn Errors in the Biosynthesis or Action of Aldosterone*

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Defects in cortisol metabolism causing low-renin hypertension

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

Clinical and biochemical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency. A study of 25 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0889-8529%2808%2970019-7

7 January 2021

10.1016/S0889-8529(08)70019-7

Identifiers

DOI

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31 July 2017

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