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HSD17B3
Clinical and Molecular Spectrum of Patients with 17Β-Hydroxysteroid
Differential but Concerted Expression of HSD17B2, HSD17B3, SHBG And
Uman Enome News
Physiological and Biochemical Aspects of 17Β-Hydroxysteroid Dehydrogenase Type 2 and 3
Gnomad Lof Supplement
Reveals of Candidate Active Ingredients in Justicia and Its Anti-Thrombotic Action of Mechanism Based on Network Pharmacology Ap
REVIEW 17Β-Hydroxysteroid Dehydrogenase (HSD)/17-Ketosteroid Reductase (KSR) Family; Nomenclature and Main Characteristics of T
Human Adrenal Corticocarcinoma NCI-H295R Cells Produce More
Table of Human SDR Enzymes with SDR Designations Version 3
17-Beta Hydroxysteroid Dehydrogenase 3 Deficiency
Elucidating the Role of 17Β Hydroxysteroid Dehydrogenase Type 14 in Normal Physiology and in Breast Cancer
NR0B1 Supporting Information Biorxiv
Mouse Hsd17b3 Knockout Project (CRISPR/Cas9)
HSD17B3 Gene Hydroxysteroid 17-Beta Dehydrogenase 3
Ablation of the Canonical Testosterone Production Pathway Via Knockout Of
Applying Forward Genetic Approaches to Rare Mendelian
Mouse Hsd17b3 Conditional Knockout Project (CRISPR/Cas9)
Functional Analyses of Endometriosis-Related Polymorphisms in the Estrogen Synthesis and Metabolism-Related Genes
Top View
Epigenetics Meets Endocrinology
17Β-Hydroxysteroid Dehydrogenase Type 3 Deficiency: Diagnosis, Phenotypic Variability and Molecular Findings
Parental Micronutrient Deficiency Distorts Liver DNA Methylation And
Genomic and Neural Analysis of the Estradiol-Synthetic Pathway in the Zebra Finch
Report on the Fifth International Workshop on Chromosome 9 Held at Eynsham, Oxfordshire, UK, September 4-6, 1996
Screening for Mutations in 17B-Hydroxysteroid Dehydrogenase and Androgen Receptor in Women Presenting with Partially Virilised 46,XY Disorders of Sex Development
Chromosomes Tetraodon and Xq Genes on Three Four-Hundred
Sox9 and Sox8 Protect the Adult Testis from Male-To-Female Genetic Reprogramming and Complete Degeneration. Running Title
A Novel Mutation Causing 17-Β-Hydroxysteroid Dehydrogenase
46,XY Disorder of Sex Development Due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek Origin
A Computational Approach to Mechanistic and Predictive