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Publications by Meilan M Rutter
Complexities of Gender Assignment in 17β-Hydroxysteroid Dehydrogenase Type 3 Deficiency: Is There a Role for Early Orchiectomy?
International Journal of Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Related publications
Undetectable Levels of CSF Amyloid-Β Peptide in a Patient With 17β-Hydroxysteroid Dehydrogenase Deficiency
Journal of Alzheimer's Disease
Gerontology
Clinical Psychology
Mental Health
Psychiatry
Geriatrics
Medicine
Neuroscience
Transcriptional Regulation of Type 11 17β-Hydroxysteroid Dehydrogenase Expression in Prostate Cancer Cells
Molecular and Cellular Endocrinology
Biochemistry
Endocrinology
Molecular Biology
Levels of 17β-Hydroxysteroid Dehydrogenase Type 10 in CSF Are Not a Valuable Biomarker for Multiple Sclerosis
Biomarkers in Medicine
Biochemistry
Drug Discovery
Clinical Biochemistry
Structural Basis for Species Specific Inhibition of 17β-Hydroxysteroid Dehydrogenase Type 1 (17β-Hsd1): Computational Study and Biological Validation
PLoS ONE
Multidisciplinary
Mild Adrenal 3.beta.-Hydroxysteroid Dehydrogenase Deficiency With Hyperaldosteronism.
Endocrinologia Japonica
High Expression of 17β-Hydroxysteroid Dehydrogenase Type 2 Is Associated With a Better Prognosis in Urothelial Carcinoma of the Urinary Tract
Journal of Cancer
Oncology
Comparative Evolutionary Genomics of the HADH2 Gene Encoding Aβ-Binding Alcohol Dehydrogenase/17β-Hydroxysteroid Dehydrogenase Type 10 (ABAD/HSD10)
BMC Genomics
Biotechnology
Genetics
Cortisone-Reductase Deficiency Associated With Heterozygous Mutations in 11 -Hydroxysteroid Dehydrogenase Type 1
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Overexpression of 17β-Hydroxysteroid Dehydrogenase Type 10 Increases Pheochromocytoma Cell Growth and Resistance to Cell Death
BMC Cancer
Cancer Research
Oncology
Genetics