Three-dimensional structure of steroid 21-hydroxylase (cytochrome P450 21A2) with two substrates reveals locations of disease-associated variants (Q34248547)

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English	Three-dimensional structure of steroid 21-hydroxylase (cytochrome P450 21A2) with two substrates reveals locations of disease-associated variants	scientific article

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20 January 2020

Three-dimensional structure of steroid 21-hydroxylase (cytochrome P450 21A2) with two substrates reveals locations of disease-associated variants (English)

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20 January 2020

Surajit Banerjee

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20 January 2020

F. Peter Guengerich

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F Peter Guengerich

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20 January 2020

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Bin Zhao

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20 January 2020

Li Lei

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20 January 2020

Norio Kagawa

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20 January 2020

Munirathinam Sundaramoorthy

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20 January 2020

Leslie D Nagy

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20 January 2020

Michael R Waterman

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18 January 2012

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20 January 2020

Journal of Biological Chemistry

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20 January 2020

287

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20 January 2020

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20 January 2020

10613-10622

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20 January 2020

Molecular genetics of 21-hydroxylase deficiency

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Monitoring of therapy in congenital adrenal hyperplasia

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6 July 2018

Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations

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6 July 2018

21-hydroxylase deficiency congenital adrenal hyperplasia

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Likelihood-enhanced fast rotation functions

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Multiparametric scaling of diffraction intensities

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6 July 2018

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3323056

6 July 2018

Structure of a cytochrome P450-redox partner electron-transfer complex

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6 July 2018

Structure of human steroid 21-hydroxylase genes

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6 July 2018

Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man

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Aberrant splicing and missense mutations cause steroid 21-hydroxylase [P-450(C21)] deficiency in humans: possible gene conversion products

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Evidence that an adrenal-specific nuclear protein regulates the cAMP responsiveness of the human CYP21B (P450C21) gene

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6 July 2018

Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

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Congenital adrenal hyperplasia.

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21 January 2018

A 3D model of human P450c21: study of the putative effects of steroid 21-hydroxylase gene mutations

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12 December 2020

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cAMP-dependent transcription of the human CYP21B (P-450C21) gene requires a cis-regulatory element distinct from the consensus cAMP-regulatory element

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12 December 2020

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Population-wide evaluation of disease manifestation in relation to molecular genotype in steroid 21-hydroxylase (CYP21) deficiency: good correlation in a well defined population

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comprehensive analytical strategy for mutation screening in 21-hydroxylase deficiency

1 reference

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12 December 2020

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inferred from PubMed ID database lookup

Functional characterization of threeCYP21A2sequence variants (p.A265V, p.W302S, p.D322G) employing a yeast co-expression system

1 reference

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inferred from PubMed ID database lookup

Expression of human cytochrome P450 2B6 in Escherichia coli: characterization of catalytic activity and expression levels in human liver

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12 December 2020

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inferred from PubMed ID database lookup

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10.1074/JBC.M111.323501

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20 January 2020

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20 January 2020

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20 January 2020

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