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Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2013, Volume 110, Issue 7, pp. 2611 - 2616
Journal Article
Journal Article
Journal Article
Medicine, ISSN 0025-7974, 08/2018, Volume 97, Issue 33, pp. e11888 - e11888
Rationale:Adrenal incidentaloma is sometimes complicated with 21-hydroxylase deficiency (21-OHD). Latent nonclassical 21-OHD in incidentaloma is difficult to... 
adrenalectomy | MEDICINE, GENERAL & INTERNAL | 21-hydroxylase deficiency | adrenal insufficiency | adrenal incidentaloma | nonclassical 21-hydroxylase deficiency | Adrenalectomy | Complications and side effects | Usage | Adrenal insufficiency | Gene mutations | Genetic aspects | Research | Diagnosis | Index Medicus | Abridged Index Medicus
Journal Article
Journal of Steroid Biochemistry and Molecular Biology, ISSN 0960-0760, 01/2017, Volume 165, Issue Pt A, pp. 38 - 50
Cytochrome P450 oxidoreductase (POR) is required for metabolic reactions of steroid and drug metabolizing cytochrome P450 proteins located in endoplasmic... 
Steroid metabolism | P450 oxidoreductase deficiency | Antley-Bixler syndrome | PORD | Disorders of sexual development | Cytochrome P450 oxidoreductase | CYP17A1 | BACKDOOR PATHWAY | 21-HYDROXYLASE DEFICIENCY | BIOCHEMISTRY & MOLECULAR BIOLOGY | CONGENITAL ADRENAL-HYPERPLASIA | IMPAIRED STEROIDOGENESIS | CYTOCHROME-P450 OXIDOREDUCTASE | GENETIC-VARIATION | ANTLEY-BIXLER-SYNDROME | STRUCTURAL BASIS | ENDOCRINOLOGY & METABOLISM | COMPOUND HETEROZYGOUS MUTATIONS | PRENATAL-DIAGNOSIS | Microsomes - metabolism | NADPH-Ferrihemoprotein Reductase - genetics | Humans | Endoplasmic Reticulum - metabolism | Male | Genetic Variation | Founder Effect | DNA Mutational Analysis | Steroids - metabolism | Female | Imaging, Three-Dimensional | Binding Sites | Oxidation-Reduction | Japan | European Continental Ancestry Group | NADPH-Ferrihemoprotein Reductase - deficiency | Molecular Dynamics Simulation | Polymorphism, Genetic | Animals | Turkey | Alleles | Protein Binding | Protein Conformation | Steroid 17-alpha-Hydroxylase - genetics | Mutation | Enzymes | Analysis | Genetic aspects | Genitalia | Oxidoreductase | Cytochrome P450 | Hyperplasia | Data processing | Metabolism | Population genetics | Proteins | Computer applications | Drug metabolism | Steroidogenesis | Xenobiotics | Endoplasmic reticulum | Steroid hormones | Steroids | Polymorphism | Index Medicus
Journal Article
Journal Article
Trends in Endocrinology & Metabolism, ISSN 1043-2760, 2008, Volume 19, Issue 3, pp. 96 - 99
Congenital adrenal hyperplasia due to steroid 11β-hydroxylase deficiency is a genetic disorder of steroidogenesis, transmitted as an autosomal recessive trait.... 
Endocrinology & Metabolism | 21-HYDROXYLASE DEFICIENCY | ALDOSTERONE SYNTHASE | ENDOCRINOLOGY & METABOLISM | UNEQUAL CROSSING-OVER | BETA-HYDROXYLASE DEFICIENCY | 11-DEOXYCORTISOL | MUTATIONS | HYPERTENSION | AMNIOTIC-FLUID | PRENATAL-DIAGNOSIS | CYP11B1 GENE
Journal Article
Journal of Steroid Biochemistry and Molecular Biology, ISSN 0960-0760, 01/2017, Volume 165, Issue Pt B, pp. 396 - 406
Journal Article
The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 08/2010, Volume 95, Issue 8, pp. 3633 - 3640
Journal Article
ENDOCRINE, ISSN 1355-008X, 03/2019, Volume 63, Issue 3, pp. 407 - 421
Journal Article
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