(Q36049127)

11 August 2017

Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency (English)

1 reference

congenital adrenal hyperplasia

11 August 2017

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1 reference

1 reference

Maria Szarras-Czapnik

44

Maria Szarras-Czapnik

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Jan Idkowiak

Jan Idkowiak

3

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Deborah Cragun

Deborah L Cragun

18

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Robert J. Hopkin

Robert J Hopkin

30

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Nils Krone

Nils Krone

1

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Wiebke Arlt

Wiebke Arlt

52

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Mehul T Dattani

19

Mehul T Dattani

1 reference

11 August 2017

33

Michiel N Kerstens

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11 August 2017

Cedric H L Shackleton

51

Cedric H L Shackleton

1 reference

11 August 2017

37

Shelly Nielsen

1 reference

11 August 2017

4

Vivek Dhir

1 reference

11 August 2017

28

Berthold P Hauffa

1 reference

11 August 2017

6

Beverly A Hughes

1 reference

11 August 2017

5

Hannah E Ivison

1 reference

11 August 2017

27

Ann Haskins Olney

1 reference

11 August 2017

Nicole Reisch

2

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11 August 2017

Ian T Rose

7

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11 August 2017

Donna M O'Neil

8

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11 August 2017

Raymon Vijzelaar

9

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11 August 2017

Matthew J Smith

10

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11 August 2017

Fiona MacDonald

11

1 reference

11 August 2017

Trevor R Cole

12

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11 August 2017

Nicolai Adolphs

13

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11 August 2017

John S Barton

14

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11 August 2017

Edward M Blair

15

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11 August 2017

Stephen R Braddock

16

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11 August 2017

Felicity Collins

17

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11 August 2017

Ruth Day

20

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11 August 2017

Shelley Dougan

21

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11 August 2017

Miriam Feist

22

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11 August 2017

Michael E Gottschalk

23

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11 August 2017

John W Gregory

24

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11 August 2017

Michaela Haim

25

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11 August 2017

Rachel Harrison

26

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11 August 2017

Peter C Hindmarsh

29

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11 August 2017

Petr E Jira

31

1 reference

11 August 2017

Marlies Kempers

32

1 reference

11 August 2017

Mohamed M Khalifa

34

1 reference

11 August 2017

Birgit Köhler

35

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11 August 2017

Dominique Maiter

36

1 reference

11 August 2017

Stephen M O'Riordan

38

1 reference

11 August 2017

Christian L Roth

39

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11 August 2017

Kate P Shane

40

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11 August 2017

Martin Silink

41

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11 August 2017

Nike M M L Stikkelbroeck

42

1 reference

11 August 2017

Elizabeth Sweeney

43

1 reference

11 August 2017

John R Waterson

45

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11 August 2017

Lori Williamson

46

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11 August 2017

Michaela F Hartmann

47

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11 August 2017

Norman F Taylor

48

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11 August 2017

Stefan A Wudy

49

1 reference

11 August 2017

Ewa M Malunowicz

50

1 reference

11 August 2017

language of work or name

English

0 references

publication date

7 December 2011

1 reference

The Journal of Clinical Endocrinology and Metabolism

11 August 2017

1 reference

11 August 2017

97

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11 August 2017

2

1 reference

11 August 2017

E257-67

1 reference

Pubertal presentation in seven patients with congenital adrenal hyperplasia due to P450 oxidoreductase deficiency

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Consequences of POR mutations and polymorphisms.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Impaired hepatic drug and steroid metabolism in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Gas chromatography/mass spectrometry (GC/MS) remains a pre-eminent discovery tool in clinical steroid investigations even in the era of fast liquid chromatography tandem mass spectrometry (LC/MS/MS).

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Concomitant mutations in the P450 oxidoreductase and androgen receptor genes presenting with 46,XY disordered sex development and androgenization at adrenarche

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Clinical, genetic, and enzymatic characterization of P450 oxidoreductase deficiency in four patients.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Genetics of congenital adrenal hyperplasia

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

The approach to the adult with newly diagnosed adrenal insufficiency

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Cholesterol metabolism: the main pathway acting downstream of cytochrome P450 oxidoreductase in skeletal development of the limb

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Cytochrome P450 oxidoreductase deficiency: identification and characterization of biallelic mutations and genotype-phenotype correlations in 35 Japanese patients

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Homozygous mutation G539R in the gene for P450 oxidoreductase in a family previously diagnosed as having 17,20-lyase deficiency.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Genetics of P450 oxidoreductase: sequence variation in 842 individuals of four ethnicities and activities of 15 missense mutations

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Modulation of human CYP19A1 activity by mutant NADPH P450 oxidoreductase

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Congenital adrenal hyperplasia and P450 oxidoreductase deficiency

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Cytochrome P450 oxidoreductase gene mutations and Antley-Bixler syndrome with abnormal genitalia and/or impaired steroidogenesis: molecular and clinical studies in 10 patients.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Prenatal diagnosis of P450 oxidoreductase deficiency (ORD): a disorder causing low pregnancy estriol, maternal and fetal virilization, and the Antley-Bixler syndrome phenotype

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Congenital adrenal hyperplasia caused by mutant P450 oxidoreductase and human androgen synthesis: analytical study

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Identification of novel roles of the cytochrome p450 system in early embryogenesis: effects on vasculogenesis and retinoic Acid homeostasis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

2 October 2017

Adrenal insufficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Association of multiple developmental defects and embryonic lethality with loss of microsomal NADPH-cytochrome P450 oxidoreductase

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Distinctive profile of the 17-hydroxylase and 17,20-lyase activities revealed by urinary steroid metabolomes of patients with CYP17 deficiency

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Rescue of cytochrome P450 oxidoreductase (Por) mouse mutants reveals functions in vasculogenesis, brain and limb patterning linked to retinoic acid homeostasis

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Linking Antley-Bixler syndrome and congenital adrenal hyperplasia: a novel case of P450 oxidoreductase deficiency

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Cytochrome P450 oxidoreductase deficiency in three patients initially regarded as having 21-hydroxylase deficiency and/or aromatase deficiency: diagnostic value of urine steroid hormone analysis

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

A male twin infant with skull deformity and elevated neonatal 17-hydroxyprogesterone: a prismatic case of P450 oxidoreductase deficiency

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Undetectable maternal serum uE3 and postnatal abnormal sterol and steroid metabolism in Antley-Bixler syndrome

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Compound heterozygous mutations of cytochrome P450 oxidoreductase gene (POR) in two patients with Antley-Bixler syndrome.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

5α-reduced C21 steroids are substrates for human cytochrome P450c17

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Abnormal sterol metabolism in a patient with Antley-Bixler syndrome and ambiguous genitalia

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Features of Antley-Bixler syndrome in an infant born to a mother with pregnancy luteoma

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3380101

Differential Inhibition of CYP17A1 and CYP21A2 Activities by the P450 Oxidoreductase Mutant A287P

23 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22162478

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Biochemical diagnosis of Antley-Bixler syndrome by steroid analysis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22162478

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1210/JC.2011-0640

1 reference

11 August 2017

1 reference

11 August 2017

PubMed publication ID

22162478

1 reference