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Publications by William E Rainey
Adrenal-Derived 11-Oxygenated 19-Carbon Steroids Are the Dominant Androgens in Classic 21-Hydroxylase Deficiency
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Role of Angiotensin II-induced Rapid Response Genes in the Regulation of Enzymes Needed for Aldosterone Synthesis
Journal of Molecular Endocrinology
Endocrinology
Molecular Biology
Related publications
Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Congenital Adrenal Hyperplasia Due to 11-Beta-Hydroxylase Deficiency
Adrenal Specific Nuclear Transcription Factor (Tf) Binding Region in 21-Hydroxylase Deficiency
Pediatric Research
Child Health
Pediatrics
Perinatology
Steroid 21-Hydroxylase Deficiency in Mice. An Animal Model for Congenital Adrenal Hyperplasia.
Proceedings of The Japanese Association of Animal Models for Human Diseases
Apparent Activities of 21-Hydroxylase, 17alpha-Hydroxylase and 17,20-Lyase Are Impaired in Adrenal Incidentalomas
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
11-Beta-Hydroxylase Deficiency
Prevalence of Testicular Adrenal Rest Tumours in Male Children With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Psychological Vulnerability to Stress in Carriers of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Hormones
Medicine
Endocrinology
Metabolism
Diabetes
Genotype-Phenotype Correlation in 1,507 Families With Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency
Proceedings of the National Academy of Sciences of the United States of America
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