Disease on EC 1.1.1.145 - 3beta-hydroxy-DELTA5-steroid dehydrogenase
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3(or 17)beta-hydroxysteroid dehydrogenase deficiency
New insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiency: identification of eight mutations in the HSD3B2 gene eleven patients from seven new families and comparison of the functional properties of twenty-five mutant enzymes.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
3beta-hydroxy-delta5-C27-steroid dehydrogenase/isomerase deficiency in a 23-year-old woman.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
A case of 3beta-hydroxysteroid dehydrogenase type II (HSD3B2) deficiency picked up by neonatal screening for 21-hydroxylase deficiency: difficulties and delay in etiologic diagnosis.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
Adrenogenital syndrome. Association with 3-beta-hydroxysteroid dehydrogenase deficiency.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
Carboxyl-Terminal Mutations in 3{beta}-Hydroxysteroid Dehydrogenase Type II Cause Severe Salt-Wasting Congenital Adrenal Hyperplasia.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
Carriers for type II 3beta-hydroxysteroid dehydrogenase (HSD3B2) deficiency can only be identified by HSD3B2 genotype study and not by hormone test.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
Case of an unreported genetic variant of salt losing 3-?-hydroxysteroid dehydrogenase deficiency.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
Co-Existence of Congenital Adrenal Hyperplasia and Bartter Syndrome due to Maternal Uniparental Isodisomy of HSD3B2 and CLCNKB Mutations.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
Comprehensive genotyping of Turkish women with hirsutism.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
CONCURRENT 3-BETA-HYDROXYSTEROID DEHYDROGENASE DEFICIENCY IN ADRENAL AND SCLEROCYSTIC OVARY.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
Elevated 17-hydroxyprogesterone and testosterone in a newborn with 3-beta-hydroxysteroid dehydrogenase deficiency.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
Human 3?-hydroxysteroid dehydrogenase deficiency seems to affect fertility but may not harbor a tumor risk: lesson from an experiment of nature.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
Molecular genetic and bile acid profiles in two Japanese patients with 3beta-hydroxy-DELTA5-C27-steroid dehydrogenase/isomerase deficiency.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
Refining hormonal diagnosis of type II 3beta-hydroxysteroid dehydrogenase deficiency in patients with premature pubarche and hirsutism based on HSD3B2 genotyping.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
Serum and urinary steroids in girls with precocious pubarche and/or hirsutism due to mild 3-beta-hydroxysteroid dehydrogenase deficiency.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
Severe Salt-Losing 3?-Hydroxysteroid Dehydrogenase Deficiency: Treatment and Outcomes of HSD3B2 c.35G>A Homozygotes.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
Steroidogenesis of the testis -- new genes and pathways.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
Testis sparing surgery for steroid unresponsive testicular tumors of the adrenogenital syndrome.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
The hormonal phenotype of Nonclassic 3 beta-hydroxysteroid dehydrogenase (HSD3B) deficiency in hyperandrogenic females is associated with insulin-resistant polycystic ovary syndrome and is not a variant of inherited HSD3B2 deficiency.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
Titration of Bile Acid Supplements in 3beta-Hydroxy-Delta5-C27-Steroid Dehydrogenase/Isomerase Deficiency.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
Two Zebrafish hsd3b Genes Are Distinct in Function, Expression, and Evolution.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
Urinary steroidal pattern of infants with congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency.
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
[Adrenal enzymatic block with late-onset caused by 11-hydroxylase deficiency. Apropos of 29 cases]
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
[Clinical features and diagnosis of mild 3-beta-hydroxysteroid dehydrogenase deficiency in men]
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
[Late onset hyperandrogenism caused by 3-beta-hydroxysteroid dehydrogenase deficiency]
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
[Partial 3-beta-hydroxysteroid dehydrogenase deficiencies]
3beta-hydroxy-delta5-steroid dehydrogenase deficiency
[Polycystic ovary syndrome as expression of 3-beta-hydroxysteroid dehydrogenase deficiency]
3beta-hydroxysteroid 3-dehydrogenase deficiency
A novel A10E homozygous mutation in the HSD3B2 gene causing severe salt-wasting 3beta-hydroxysteroid dehydrogenase deficiency in 46,XX and 46,XY French-Canadians: evaluation of gonadal function after puberty.
3beta-hydroxysteroid 3-dehydrogenase deficiency
Mutations in the type II 3beta-hydroxysteroid dehydrogenase (HSD3B2) gene can cause premature pubarche in girls.
3beta-hydroxysteroid 3-dehydrogenase deficiency
New insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiency: identification of eight mutations in the HSD3B2 gene eleven patients from seven new families and comparison of the functional properties of twenty-five mutant enzymes.
3beta-hydroxysteroid 3-dehydrogenase deficiency
Refining hormonal diagnosis of type II 3beta-hydroxysteroid dehydrogenase deficiency in patients with premature pubarche and hirsutism based on HSD3B2 genotyping.
Adrenal Hyperplasia, Congenital
A case of 3beta-hydroxysteroid dehydrogenase type II (HSD3B2) deficiency picked up by neonatal screening for 21-hydroxylase deficiency: difficulties and delay in etiologic diagnosis.
Adrenal Hyperplasia, Congenital
A New Homozygous Frameshift Mutation in the HSD3B2 Gene in an Apparently Nonconsanguineous Italian Family.
Adrenal Hyperplasia, Congenital
A new insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiency.
Adrenal Hyperplasia, Congenital
A novel A10E homozygous mutation in the HSD3B2 gene causing severe salt-wasting 3beta-hydroxysteroid dehydrogenase deficiency in 46,XX and 46,XY French-Canadians: evaluation of gonadal function after puberty.
Adrenal Hyperplasia, Congenital
A Novel Homozygous Q334X Mutation in the HSD3B2 Gene Causing Classic 3?-Hydroxysteroid Dehydrogenase Deficiency: An Unexpected Diagnosis after a Positive Newborn Screen for 21-Hydroxylase Deficiency.
Adrenal Hyperplasia, Congenital
A novel missense mutation in the HSD3B2 gene, underlying nonsalt-wasting congenital adrenal hyperplasia. new insight into the structure-function relationships of 3?-hydroxysteroid dehidrogenase type II.
Adrenal Hyperplasia, Congenital
Birth of a healthy boy following preimplantation genetic diagnosis for congenital adrenal hyperplasia.
Adrenal Hyperplasia, Congenital
Carboxyl-Terminal Mutations in 3{beta}-Hydroxysteroid Dehydrogenase Type II Cause Severe Salt-Wasting Congenital Adrenal Hyperplasia.
Adrenal Hyperplasia, Congenital
Carriers for type II 3beta-hydroxysteroid dehydrogenase (HSD3B2) deficiency can only be identified by HSD3B2 genotype study and not by hormone test.
Adrenal Hyperplasia, Congenital
Co-Existence of Congenital Adrenal Hyperplasia and Bartter Syndrome due to Maternal Uniparental Isodisomy of HSD3B2 and CLCNKB Mutations.
Adrenal Hyperplasia, Congenital
Congenital adrenal hyperplasia due to 3beta-hydroxysteroid dehydrogenase/Delta(5)-Delta(4) isomerase deficiency.
Adrenal Hyperplasia, Congenital
Late diagnosis of 3?-Hydroxysteroid dehydrogenase deficiency: the pivotal role of gas chromatography-mass spectrometry urinary steroid metabolome analysis and a novel homozygous nonsense mutation in the HSD3B2 gene.
Adrenal Hyperplasia, Congenital
New insight into the molecular basis of 3beta-hydroxysteroid dehydrogenase deficiency: identification of eight mutations in the HSD3B2 gene eleven patients from seven new families and comparison of the functional properties of twenty-five mutant enzymes.
Adrenal Hyperplasia, Congenital
Non-Virilizing Congenital Adrenal Hyperplasia in a Female Patient with a Novel HSD3B2 Mutation.
Adrenal Hyperplasia, Congenital
Refining hormonal diagnosis of type II 3beta-hydroxysteroid dehydrogenase deficiency in patients with premature pubarche and hirsutism based on HSD3B2 genotyping.
Adrenal Hyperplasia, Congenital
Severe Salt-Losing 3?-Hydroxysteroid Dehydrogenase Deficiency: Treatment and Outcomes of HSD3B2 c.35G>A Homozygotes.
Adrenal Hyperplasia, Congenital
Structural aspects of the p.P222Q homozygous mutation of HSD3B2 gene in a patient with congenital adrenal hyperplasia.
Adrenal Hyperplasia, Congenital
Three cases of 3?-hydroxysteroid dehydrogenase deficiency: Clinical analysis.
Adrenal Hyperplasia, Congenital
Two Zebrafish hsd3b Genes Are Distinct in Function, Expression, and Evolution.
Adrenal Hyperplasia, Congenital
Unusual type of congenital adrenal hyperplasia probably due to deficiency of 3-beta-hydroxysteroid dehydrogenase. Case report of a surviving girl and steroid studies.
Adrenal Hyperplasia, Congenital
Urinary steroidal pattern of infants with congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency.
Adrenal Hyperplasia, Congenital
[A novel homozygous mutation p.E25X in the HSD3B2 gene causing salt wasting 3?-hydroxysteroid dehydrogenases deficiency in a Chinese pubertal girl: a delayed diagnosis until recurrent ovary cysts].
Adrenal Hyperplasia, Congenital
[Congenital adrenal hyperplasia due to blockade of 3-beta-hydroxysteroid dehydrogenase]
Adrenocortical Carcinoma
Differential regulation of 3beta-hydroxysteroid dehydrogenase type II and 17alpha-hydroxylase/lyase P450 in human adrenocortical carcinoma cells by epidermal growth factor and basic fibroblast growth factor.
Adrenocortical Carcinoma
Sunitinib Inhibits Cell Proliferation and Alters Steroidogenesis by Down-Regulation of HSD3B2 in Adrenocortical Carcinoma Cells.
Adrenogenital Syndrome
Adrenogenital syndrome. Association with 3-beta-hydroxysteroid dehydrogenase deficiency.
Bartter Syndrome
Co-Existence of Congenital Adrenal Hyperplasia and Bartter Syndrome due to Maternal Uniparental Isodisomy of HSD3B2 and CLCNKB Mutations.
Breast Neoplasms
Genomic Profiling of the Steroidogenic Acute Regulatory Protein in Breast Cancer: In Silico Assessments and a Mechanistic Perspective.
Breast Neoplasms
Structural basis for the selective inhibition of human 3beta-hydroxysteroid dehydrogenase 1 in human breast tumor MCF-7 cells.
Cryptorchidism
A rare variety of congenital adrenal hyperplasia with mosaic Klinefelter syndrome: a unique combination presenting with ambiguous genitalia and sexual precocity
Cysts
The steroid hormone environment during primordial follicle formation in perinatal mouse ovaries.
Disorders of Sex Development
A New Homozygous Frameshift Mutation in the HSD3B2 Gene in an Apparently Nonconsanguineous Italian Family.
Disorders of Sex Development
A rare variety of congenital adrenal hyperplasia with mosaic Klinefelter syndrome: a unique combination presenting with ambiguous genitalia and sexual precocity
Disorders of Sex Development
Late diagnosis of 3?-Hydroxysteroid dehydrogenase deficiency: the pivotal role of gas chromatography-mass spectrometry urinary steroid metabolome analysis and a novel homozygous nonsense mutation in the HSD3B2 gene.
Disorders of Sex Development
Refining hormonal diagnosis of type II 3beta-hydroxysteroid dehydrogenase deficiency in patients with premature pubarche and hirsutism based on HSD3B2 genotyping.
Disorders of Sex Development
Structural aspects of the p.P222Q homozygous mutation of HSD3B2 gene in a patient with congenital adrenal hyperplasia.
Endometrial Neoplasms
The nuclear receptors SF1 and LRH1 are expressed in endometrial cancer cells and regulate steroidogenic gene transcription by cooperating with AP-1 factors.
Endometriosis
HSD3B2, HSD17B1, HSD17B2, ESR1, ESR2 and AR expression in infertile women with endometriosis.
Endometriosis
Intra-tissue steroid profiling indicates differential progesterone and testosterone metabolism in the endometrium and endometriosis lesions.
Essential Hypertension
Association of HSD3B1 and HSD3B2 gene polymorphisms with essential hypertension, aldosterone level, and left ventricular structure.
Genetic Diseases, Inborn
Aetiology of hypospadias: a systematic review of genes and environment.
Glioma
miR-29a-5p Regulates the Proliferation, Invasion, and Migration of Gliomas by Targeting DHRS4.
Herpes Zoster
A case of primary aldosteronism caused by multiple adrenocortical macronodules.
Herpes Zoster
Development of monoclonal antibodies against the human 3?-hydroxysteroid dehydrogenase/isomerase isozymes.
Herpes Zoster
DNA methylation is not involved in specific down-regulation of HSD3B2, NR4A1 and RARB genes in androgen-secreting cells of human adrenal cortex.
Herpes Zoster
Human adrenal cells that express both 3?-hydroxysteroid dehydrogenase type 2 (HSD3B2) and cytochrome b5 (CYB5A) contribute to adrenal androstenedione production.
Herpes Zoster
Human adrenal corticocarcinoma NCI-H295R cells produce more androgens than NCI-H295A cells and differ in 3beta-hydroxysteroid dehydrogenase type 2 and 17,20 lyase activities.
Herpes Zoster
Immunolocalization of murine type VI 3?-hydroxysteroid dehydrogenase in the adrenal gland, testis, skin, and placenta.
Herpes Zoster
[Effects of infrasound on activities of 3beta hydroxysteroid dehydrogenase and acid phosphatase of polygonal cells in adrenal cortex zona fasciculate in mice]
Hirsutism
Genotyping of the type II 3beta-hydroxysteroid dehydrogenase gene (HSD3B2) in women with hirsutism and elevated ACTH-stimulated delta(5)-steroids.
Hirsutism
Refining hormonal diagnosis of type II 3beta-hydroxysteroid dehydrogenase deficiency in patients with premature pubarche and hirsutism based on HSD3B2 genotyping.
Hirsutism
Serum and urinary steroids in girls with precocious pubarche and/or hirsutism due to mild 3-beta-hydroxysteroid dehydrogenase deficiency.
Hyperaldosteronism
Development of monoclonal antibodies against the human 3?-hydroxysteroid dehydrogenase/isomerase isozymes.
Hyperandrogenism
Baicalin inhibits recruitment of GATA1 to the HSD3B2 promoter and reverses hyperandrogenism of PCOS.
Hyperandrogenism
Nonhuman primates as models for human adrenal androgen production: Function and dysfunction.
Hyperandrogenism
Variants of the type II 3beta-hydroxysteroid dehydrogenase gene in children with premature pubic hair and hyperandrogenic adolescents.
Hyperandrogenism
[Late onset hyperandrogenism caused by 3-beta-hydroxysteroid dehydrogenase deficiency]
Hypertension
Salt-sensitive hypertension in circadian clock-deficient Cry-null mice involves dysregulated adrenal Hsd3b6.
Hypertrophy, Left Ventricular
Association of HSD3B1 and HSD3B2 gene polymorphisms with essential hypertension, aldosterone level, and left ventricular structure.
Hypogonadism
A rare variety of congenital adrenal hyperplasia with mosaic Klinefelter syndrome: a unique combination presenting with ambiguous genitalia and sexual precocity
Hypogonadism
[3-Beta-hydroxysteroid dehydrogenase activity in hypogonadotropic hypogonadism]
Hypospadias
Late diagnosis of 3?-Hydroxysteroid dehydrogenase deficiency: the pivotal role of gas chromatography-mass spectrometry urinary steroid metabolome analysis and a novel homozygous nonsense mutation in the HSD3B2 gene.
Hypospadias
Maternal exposure to di-n-butyl phthalate (DBP) induces combined anorectal and urogenital malformations in male rat offspring.
Hypospadias
Molecular study of the 3 beta-hydroxysteroid dehydrogenase gene type II in patients with hypospadias.
Hypospadias
Production of congenital adrenal cortical hyperplasia, hypospadias, and clitoral hypertrophy (adrenogenital syndrome) in rats by inactivation of 3-beta-hydroxysteroid dehydrogenase.
Hypotension
Term neonates with infection and shock display high cortisol precursors despite low levels of normal cortisol.
Infections
Testosterone response of hepatic gene expression in female mice having acquired testosterone-unresponsive immunity to Plasmodium chabaudi malaria.
Infections
The orphan nuclear receptor NGFIB regulates transcription of 3beta-hydroxysteroid dehydrogenase. implications for the control of adrenal functional zonation.
Insulin Resistance
The hormonal phenotype of Nonclassic 3 beta-hydroxysteroid dehydrogenase (HSD3B) deficiency in hyperandrogenic females is associated with insulin-resistant polycystic ovary syndrome and is not a variant of inherited HSD3B2 deficiency.
Leiomyoma
[Effects of metformin on the expression of estrogen synthetase and ER mRNA in uterine leiomyoma tissues].
Lymphatic Metastasis
Up regulation of the steroid hormone synthesis regulator HSD3B2 is linked to early PSA recurrence in prostate cancer.
Mania
Polymorphisms in AKR1C4 and HSD3B2 and differences in serum DHEAS and progesterone are associated with paranoid ideation during mania or hypomania in bipolar disorder.
Neoplasm Metastasis
Up regulation of the steroid hormone synthesis regulator HSD3B2 is linked to early PSA recurrence in prostate cancer.
Neoplasms
Benign cortisol-secreting adrenocortical adenomas produce small amounts of androgens.
Neoplasms
Cushing's Syndrome by Left Adrenocortical Adenoma Synchronously Associated with Primary Aldosteronism by Right Adrenocortical Adenoma: Report of a Case.
Neoplasms
DNA methylation is not involved in specific down-regulation of HSD3B2, NR4A1 and RARB genes in androgen-secreting cells of human adrenal cortex.
Neoplasms
Expression of steroidogenic enzymes and their transcription factors in cortisol-producing adrenocortical adenomas: immunohistochemical analysis and quantitative real-time polymerase chain reaction studies.
Neoplasms
Genomic analysis of cancer tissue reveals that somatic mutations commonly occur in a specific motif.
Neoplasms
Genomic Profiling of the Steroidogenic Acute Regulatory Protein in Breast Cancer: In Silico Assessments and a Mechanistic Perspective.
Neoplasms
Gonadotropin, steroid, and thyroid hormone milieu of young SWR mice bearing spontaneous granulosa cell tumors.
Neoplasms
Intratumoral steroid profiling of adrenal cortisol-producing adenomas by liquid chromatography- mass spectrometry.
Neoplasms
Multiple Endocrine Neoplasia Type 1 (MEN1) knockout mice develop parathyroid, pancreatic, pituitary and adrenal tumours with hypercalcaemia, hypophosphataemia and hypercorticosteronaemia.
Neoplasms
The higher affinity of human type 1 3beta-hydroxysteroid dehydrogenase (3beta-HSD1) for substrate and inhibitor steroids relative to human 3beta-HSD2 is validated in MCF-7 tumor cells and related to subunit interactions.
Neoplasms
THE HISTOCHEMISTRY OF 3-BETA-HYDROXYSTEROID DEHYDROGENASE. I. WITH SPECIAL REFERENCE TO ADRENAL GLANDS, AS AFFECTED BY ACTH, COLD, TRAUMA, AND TUMOR.
Neoplasms
TMPRSS2-ERG fusions confer efficacy of enzalutamide in an in vivo bone tumor growth model.
Neoplasms
Up regulation of the steroid hormone synthesis regulator HSD3B2 is linked to early PSA recurrence in prostate cancer.
Neoplasms
[Deficiency of 3-beta-hydroxysteroid dehydrogenase in endocrine-active tumor of the ovary]
Neuroblastoma
Alternative transcription initiation and splicing variants of the DHRS4 gene cluster.
Obesity
m6A mRNA methylation regulates testosterone synthesis through modulating autophagy in Leydig cells.
Ovarian Hyperstimulation Syndrome
The direct and indirect effects of kisspeptin-54 on granulosa lutein cell function.
Polycystic Ovary Syndrome
A Dietary Medium-Chain Fatty Acid, Decanoic Acid, Inhibits Recruitment of Nur77 to the HSD3B2 Promoter In Vitro and Reverses Endocrine and Metabolic Abnormalities in a Rat Model of Polycystic Ovary Syndrome.
Polycystic Ovary Syndrome
CONCURRENT 3-BETA-HYDROXYSTEROID DEHYDROGENASE DEFICIENCY IN ADRENAL AND SCLEROCYSTIC OVARY.
Polycystic Ovary Syndrome
Differential regulation of human 3?-hydroxysteroid dehydrogenase type 2 for steroid hormone biosynthesis by starvation and cyclic AMP stimulation: studies in the human adrenal NCI-H295R cell model.
Polycystic Ovary Syndrome
The hormonal phenotype of Nonclassic 3 beta-hydroxysteroid dehydrogenase (HSD3B) deficiency in hyperandrogenic females is associated with insulin-resistant polycystic ovary syndrome and is not a variant of inherited HSD3B2 deficiency.
Polycystic Ovary Syndrome
[Polycystic ovary syndrome as expression of 3-beta-hydroxysteroid dehydrogenase deficiency]
Prostatic Neoplasms
GEN GEN: the genomic genetic analysis of androgen-metabolic genes and prostate cancer as a paradigm for the dissection of complex phenotypes.
Prostatic Neoplasms
Genetic variation of 3 beta-hydroxysteroid dehydrogenase type II in three racial/ethnic groups: implications for prostate cancer risk.
Prostatic Neoplasms
Joint effect of HSD3B1 and HSD3B2 genes is associated with hereditary and sporadic prostate cancer susceptibility.
Prostatic Neoplasms
Modulation of AKR1C2 by curcumin decreases testosterone production in prostate cancer.
Prostatic Neoplasms
Pomegranate polyphenols down-regulate expression of androgen-synthesizing genes in human prostate cancer cells overexpressing the androgen receptor.
Prostatic Neoplasms
Single and multigenic analysis of the association between variants in 12 steroid hormone metabolism genes and risk of prostate cancer.
Prostatic Neoplasms
SRD5A2 and HSD3B2 polymorphisms are associated with prostate cancer risk and aggressiveness.
Prostatic Neoplasms
Thyroid cancer susceptibility and THRA1 and BAT-40 repeats polymorphisms.
Prostatic Neoplasms
Up regulation of the steroid hormone synthesis regulator HSD3B2 is linked to early PSA recurrence in prostate cancer.
Prostatic Neoplasms
Variant in sex hormone-binding globulin gene and the risk of prostate cancer.
Puberty, Precocious
A rare variety of congenital adrenal hyperplasia with mosaic Klinefelter syndrome: a unique combination presenting with ambiguous genitalia and sexual precocity
Puberty, Precocious
Association study of six activity SNPS in adrenal steroid hormone metabolism and IBM related genes with precocious puberty in Chinese girls.
Starvation
Impact of differential P450c17 phosphorylation by cAMP stimulation and by starvation conditions on enzyme activities and androgen production in NCI-H295R cells.
Starvation
Retinoic acid receptor beta and angiopoietin-like protein 1 are involved in the regulation of human androgen biosynthesis.
Starvation
Role of AMP-activated protein kinase on steroid hormone biosynthesis in adrenal NCI-H295R cells.
steroid 21-monooxygenase deficiency
A case of 3beta-hydroxysteroid dehydrogenase type II (HSD3B2) deficiency picked up by neonatal screening for 21-hydroxylase deficiency: difficulties and delay in etiologic diagnosis.
steroid 21-monooxygenase deficiency
A Novel Homozygous Q334X Mutation in the HSD3B2 Gene Causing Classic 3?-Hydroxysteroid Dehydrogenase Deficiency: An Unexpected Diagnosis after a Positive Newborn Screen for 21-Hydroxylase Deficiency.
steroid 21-monooxygenase deficiency
Severe Salt-Losing 3?-Hydroxysteroid Dehydrogenase Deficiency: Treatment and Outcomes of HSD3B2 c.35G>A Homozygotes.
steroid 21-monooxygenase deficiency
Testis sparing surgery for steroid unresponsive testicular tumors of the adrenogenital syndrome.
steroid delta-isomerase deficiency
Carboxyl-Terminal Mutations in 3{beta}-Hydroxysteroid Dehydrogenase Type II Cause Severe Salt-Wasting Congenital Adrenal Hyperplasia.
steroid delta-isomerase deficiency
Congenital adrenal hyperplasia due to 3beta-hydroxysteroid dehydrogenase/Delta(5)-Delta(4) isomerase deficiency.
steroid delta-isomerase deficiency
Molecular biology of the 3beta-hydroxysteroid dehydrogenase/delta5-delta4 isomerase gene family.
Urinary Bladder Neoplasms
HSD3B and gene-gene interactions in a pathway-based analysis of genetic susceptibility to bladder cancer.
Vaccinia
Effect of 3-beta-hydroxysteroid dehydrogenase gene deletion on virulence and immunogenicity of different vaccinia viruses and their recombinants.
Wilms Tumor
Isolation of definitive zone and chromaffin cells based upon expression of CD56 (neural cell adhesion molecule) in the human fetal adrenal gland.
Wilms Tumor
m6A mRNA methylation regulates testosterone synthesis through modulating autophagy in Leydig cells.
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