(Q34213892)

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Mutations in the genes encoding 11beta-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency

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31 July 2017

Mutations in the genes encoding 11beta-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency (English)

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Europe PubMed Central

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31 July 2017

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17

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Paul M Stewart

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David W Ray

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Wiebke Arlt

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Jeremy W Tomlinson

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Jeremy W Tomlinson

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Martin Hewison

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31 July 2017

Cedric H L Shackleton

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Cedric H L Shackleton

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31 July 2017

1

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Nicole Draper

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31 July 2017

Susan M Chalder

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Susan M Chalder

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31 July 2017

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Elizabeth A Walker

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31 July 2017

Iwona J Bujalska

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31 July 2017

Gareth G Lavery

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31 July 2017

Oliver Bedendo

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31 July 2017

Ian Laing

10

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31 July 2017

Ewa Malunowicz

11

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31 July 2017

Perrin C White

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31 July 2017

Philip J Mason

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31 July 2017

John M Connell

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31 July 2017

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publication date

1 August 2003

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31 July 2017

Nature Genetics

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31 July 2017

34

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31 July 2017

4

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31 July 2017

434-439

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31 July 2017

Expression of 11 beta-hydroxysteroid dehydrogenase using recombinant vaccinia virus

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

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Functional expression, characterization, and purification of the catalytic domain of human 11-beta -hydroxysteroid dehydrogenase type 1.

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

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Lumenal orientation and post-translational modifications of the liver microsomal 11 beta-hydroxysteroid dehydrogenase

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

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A possible role for microsomal hexose-6-phosphate dehydrogenase in microsomal electron transport and mixed-function oxygenase activity

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

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Polycystic ovary syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

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Hypertension in the syndrome of apparent mineralocorticoid excess due to mutation of the 11 beta-hydroxysteroid dehydrogenase type 2 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

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Cortisol effects on body mass, blood pressure, and cholesterol in the general population

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

inferred from DOI database lookup

Does central obesity reflect "Cushing's disease of the omentum"?

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

inferred from DOI database lookup

Transcriptional influence of two poly purine-pyrimidine tracts located in the HSD11B2 (11beta-hydroxysteroid dehydrogenase type 2) gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

inferred from DOI database lookup

Glucose-6-phosphate dehydrogenase: a "housekeeping" enzyme subject to tissue-specific regulation by hormones, nutrients, and oxidant stress

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

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Glucose dehydrogenase (hexose 6-phosphate dehydrogenase) and the microsomal electron transport system. Evidence supporting their possible functional relationship

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

inferred from DOI database lookup

Human hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) encoded at 1p36: coding sequence and expression

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

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Hyperandrogenism in polycystic ovary syndrome. Evidence of dysregulation of 11 beta-hydroxysteroid dehydrogenase

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

inferred from DOI database lookup

Subcellular targeting analysis of SDR-type hydroxysteroid dehydrogenases

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

inferred from DOI database lookup

Beyond Mendel: an evolving view of human genetic disease transmission

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

inferred from DOI database lookup

Digenic inheritance of severe insulin resistance in a human pedigree

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

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Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

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Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

inferred from DOI database lookup

Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT.

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

inferred from DOI database lookup

11beta-hydroxysteroid dehydrogenase type 1 knockout mice show attenuated glucocorticoid-inducible responses and resist hyperglycemia on obesity or stress

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

inferred from DOI database lookup

A transgenic model of visceral obesity and the metabolic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

inferred from DOI database lookup

Selective inhibition of 11beta-hydroxysteroid dehydrogenase type 1 decreases blood glucose concentrations in hyperglycaemic mice

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

inferred from DOI database lookup

Osteoblastic 11beta-hydroxysteroid dehydrogenase type 1 activity increases with age and glucocorticoid exposure

1 reference

https://api.crossref.org/works/10.1038%2FNG1214

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

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Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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