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17[alpha]-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the CYP17A1 Gene

Hormone research in paediatrics, 2014-06, Vol.81 (5), p.350-355

2014

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17α-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the CYP17A1 Gene

Hormone research in paediatrics, 2014, Vol.81 (5), p.350-355

2014

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46,XY Disorder of Sex Development in a Sudanese Patient Caused by a Novel Mutation in the HSD17B3 Gene

Sexual development, 2014-01, Vol.8 (4), p.151-155

2014

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The A645D Mutation in the Hinge Region of the Human Androgen Receptor (AR) Gene Modulates AR Activity, Depending on the Context of the Polymorphic Glutamine and Glycine Repeats

The journal of clinical endocrinology and metabolism, 2006-09, Vol.91 (9), p.3515-3520

2006

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Aberrant phase separation and nucleolar dysfunction in rare genetic diseases

Nature (London), 2023-02, Vol.614 (7948), p.564-4

2023

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The Action of Reproductive Fluids and Contained Steroids, Prostaglandins, and Zn2+ on CatSper Ca2+ Channels in Human Sperm

Frontiers in cell and developmental biology, 2021-07, Vol.9, p.699554-699554

2021

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The adrenal steroid profile in adolescent depression: a valuable bio-readout?

Translational psychiatry, 2022-06, Vol.12 (1), p.255-255, Article 255

2022

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Age and skin site related differences in steroid metabolism in male skin point to a key role of sebocytes in cutaneous hormone metabolism

Dermato-endocrinology, 2012-01, Vol.4 (1), p.58-64

2012

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Age at menarche relates to depression in adolescent girls: Comparing a clinical sample to the general pediatric population

Journal of affective disorders, 2022-12, Vol.318, p.103-112

2022

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The Aldosterone/Renin Ratio as a Diagnostic Tool for the Diagnosis of Primary Hypoaldosteronism in Newborns and Infants

Hormone research in paediatrics, 2015-01, Vol.84 (1), p.43-48

2015

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Analyzing the Functional and Structural Consequences of Two Point Mutations (P94L and A368D) in the CYP11B1 Gene Causing Congenital Adrenal Hyperplasia Resulting from 11-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2006-07, Vol.91 (7), p.2682-2688

2006

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Androgen action

Endocrine development, 2014, Vol.27, p.28

2014

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Androgen receptor function links human sexual dimorphism to DNA methylation

PloS one, 2013-09, Vol.8 (9), p.e73288-e73288

2013

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Androgen receptor gene mutations in androgen insensitivity syndrome cause distinct patterns of reduced activation of androgen-responsive promoter constructs

The Journal of steroid biochemistry and molecular biology, 2006-09, Vol.101 (1), p.1-10

2006

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Apolipoprotein D (APOD) is a putative biomarker of androgen receptor function in androgen insensitivity syndrome

Journal of molecular medicine (Berlin, Germany), 2009-06, Vol.87 (6), p.623-632

2009

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Area Deprivation and Regional Disparities in Treatment and Outcome Quality of 29,284 Pediatric Patients With Type 1 Diabetes in Germany: A Cross-sectional Multicenter DPV Analysis

Diabetes care, 2018-12, Vol.41 (12), p.2517-2525

2018

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The basis of gender assignment in disorders of somatosexual differentiation

Hormone research, 2005-01, Vol.64 Suppl 2, p.18-22

2005

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Behavior and circadian glucocorticoids in prepubertal monozygotic twins with birthweight differences: A prospective longitudinal cohort study on twin-to-twin transfusion syndrome patients

Psychoneuroendocrinology, 2024-09, Vol.167, p.107082-107082, Article 107082

2024

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Besonderheiten der Geschlechtsentwicklung

Pädiatrische Endokrinologie und Diabetologie, p.499-519

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Birth Weight in Different Etiologies of Disorders of Sex Development

The journal of clinical endocrinology and metabolism, 2017-03, Vol.102 (3), p.1044-1050

2017

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Carboxyl-terminal mutations in 3beta-hydroxysteroid dehydrogenase type II cause severe salt-wasting congenital adrenal hyperplasia

The journal of clinical endocrinology and metabolism, 2008-04, Vol.93 (4), p.1418-1425

2008

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Carboxyl-Terminal Mutations in 3β-Hydroxysteroid Dehydrogenase Type II Cause Severe Salt-Wasting Congenital Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2008-04, Vol.93 (4), p.1418-1425

2008

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Cell-line and tissue-specific signatures of androgen receptor-coregulator transcription

Journal of molecular medicine (Berlin, Germany), 2006-11, Vol.84 (11), p.919-931

2006

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Changes over time in sex assignment for disorders of sex development

Pediatrics (Evanston), 2014-09, Vol.134 (3), p.e710

2014

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17[alpha]-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the CYP17A1 Gene

17α-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the CYP17A1 Gene

46,XY Disorder of Sex Development in a Sudanese Patient Caused by a Novel Mutation in the HSD17B3 Gene

The A645D Mutation in the Hinge Region of the Human Androgen Receptor (AR) Gene Modulates AR Activity, Depending on the Context of the Polymorphic Glutamine and Glycine Repeats

Aberrant phase separation and nucleolar dysfunction in rare genetic diseases

The Action of Reproductive Fluids and Contained Steroids, Prostaglandins, and Zn2+ on CatSper Ca2+ Channels in Human Sperm

The adrenal steroid profile in adolescent depression: a valuable bio-readout?

Age and skin site related differences in steroid metabolism in male skin point to a key role of sebocytes in cutaneous hormone metabolism

Age at menarche relates to depression in adolescent girls: Comparing a clinical sample to the general pediatric population

The Aldosterone/Renin Ratio as a Diagnostic Tool for the Diagnosis of Primary Hypoaldosteronism in Newborns and Infants

Analyzing the Functional and Structural Consequences of Two Point Mutations (P94L and A368D) in the CYP11B1 Gene Causing Congenital Adrenal Hyperplasia Resulting from 11-Hydroxylase Deficiency

Androgen action

Androgen receptor function links human sexual dimorphism to DNA methylation

Androgen receptor gene mutations in androgen insensitivity syndrome cause distinct patterns of reduced activation of androgen-responsive promoter constructs

Apolipoprotein D (APOD) is a putative biomarker of androgen receptor function in androgen insensitivity syndrome

Area Deprivation and Regional Disparities in Treatment and Outcome Quality of 29,284 Pediatric Patients With Type 1 Diabetes in Germany: A Cross-sectional Multicenter DPV Analysis

The basis of gender assignment in disorders of somatosexual differentiation

Behavior and circadian glucocorticoids in prepubertal monozygotic twins with birthweight differences: A prospective longitudinal cohort study on twin-to-twin transfusion syndrome patients

Besonderheiten der Geschlechtsentwicklung

Biological characterization of adult MYC-translocation-positive mature B-cell lymphomas other than molecular Burkitt lymphoma

Birth Weight in Different Etiologies of Disorders of Sex Development

Carboxyl-terminal mutations in 3beta-hydroxysteroid dehydrogenase type II cause severe salt-wasting congenital adrenal hyperplasia

Carboxyl-Terminal Mutations in 3β-Hydroxysteroid Dehydrogenase Type II Cause Severe Salt-Wasting Congenital Adrenal Hyperplasia

Cell-line and tissue-specific signatures of androgen receptor-coregulator transcription

Changes over time in sex assignment for disorders of sex development

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