Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency.

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Hypokalemia: a clinical update.Unravelling drug-induced hypertension: molecular mechanisms of aldosterone-independent mineralocorticoid receptor activation by posaconazole

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Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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Clinical, genetic, and structu ...... hydrogenase type 2 deficiency.

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Clinical, genetic, and structu ...... hydrogenase type 2 deficiency.

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type

Item

label

Clinical, genetic, and structu ...... hydrogenase type 2 deficiency.

@en

Clinical, genetic, and structu ...... hydrogenase type 2 deficiency.

@nl

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Clinical, genetic, and structu ...... hydrogenase type 2 deficiency.

@en

Clinical, genetic, and structu ...... hydrogenase type 2 deficiency.

@nl

P1476

Clinical, genetic, and structu ...... hydrogenase type 2 deficiency.

@en

P2093

Ahmed Khattab

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Aisha Al Senani

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Aysenur Toygar

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Chen Ling

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Hanan Said Al Azkawi

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Hatice Nur Ozdemir

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John W Funder

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Jozef Hertecant

http://www.w3.org/2001/XMLSchema#string

Li Sun

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Mabel Yau

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P2860

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

Molecular basis for hypertension in the "type II variant" of apparent mineralocorticoid excess

Improved side-chain torsion potentials for the Amber ff99SB protein force field

Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency

A genetic defect resulting in mild low-renin hypertension

Pseudo-symmetry of C19 steroids, alternative binding orientations, and multispecificity in human estrogenic 17beta-hydroxysteroid dehydrogenase

Crystal structure of human estrogenic 17 beta-hydroxysteroid dehydrogenase complexed with 17 beta-estradiol

Unusual charge stabilization of NADP+ in 17beta-hydroxysteroid dehydrogenase

The Amber biomolecular simulation programs

Stereochemical quality of protein structure coordinates

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E11248-E11256

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scholarly article

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10.1073/PNAS.1716621115

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English

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114

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Shozeb Haider

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2017-12-11T00:00:00Z

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29229831

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Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency.

about

P2860

P2860

Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932