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Research 121–150 of 1000+
- Recent Advances in Drug Design and Drug Discovery for Androgen- Dependent Diseases
- Effects of <i>In Utero</i> Exposure to D-004, a Lipid Extract from <i>Roystonea regia</i> Fruits, in the Male Rat: A Comparison with Finasteride
- Clinical benefits and adverse effects of genetically-elevated free testosterone levels: a Mendelian randomization analysis
- Role of 5α-reductase inhibitors in androgen-stimulated skin disorders.
- 복분자 미숙과 추출물이 전립선암 세포주와 전립선비대 백서모델에 미치는 영향
- High-performance liquid chromatographic determination of the enantiomers of the benzoquinolinone LY 191704, a human type 1 5α-reductase inhibitor, in plasma
- African Journal of Biomedical Research
- Structural basis for the catalysis and inhibition of human steroid 5α‐reductase 2
- UP-02.011 Biofeedback Treatment for Dysfunctional Voiding Diagnosed in Adulthood
- Meta-Analysis of Randomized Clinical Trials of Finasteride
- Steroidal 5α-reductase and 17α-hydroxylase/17,20-lyase (CYP17) inhibitors useful in the treatment of prostatic diseases
- The search for bioactive compounds in tropical plants to target hormone imbalance associated diseases
- 17α-Acetoxy-6-bromo-16β-methylpregna-4,6-diene-3,20-dione
- Synthesis, Characterization and Evaluation of 5α, 6β-Dihalo Androsterone Derivatives as 5α-Reductase Inhibitors
- Structure of human type II 5 alpha-reductase gene.
- Pre-receptor regulation of the androgen receptor
- Significance of the polyglutamine tract polymorphism in the androgen receptor
- Selective non-steroidal inhibitors of 5α-reductase type 1
- Acute urinary retention: risks and management.
- Effect of finasteride and/or terazosin on serum PSA: Results of VA cooperative study #359
- Finasteride: The First 5α-Reductase Inhibitor
- Recent Advances in the Chemistry and Pharmacological Activity of New Steroidal Antiandrogens and 5α-Reductase Inhibitors
- Therapeutic Androgen Receptor Ligands
- 5-Alpha-Reductase Inhibitors and Combination Therapy
- Finasteride for prostatic disease: an updated and comprehensive review
- New approach to 3-oxo-4-aza-5α-androst-1-ene-17β-(--butylcarboxamide)
- Finasterida: Diez Años De Uso Clínico. Revisión Sistemática De La Literatura
- Highly efficient nucleophilic addition of alkyl Grignard reagents to 17-ketosteroids in the presence of cerium(III) chloride: Synthesis of 17α-propyl-17β-hydroxy-4-androsten-3-one, an androgen receptor antagonist
- PCPT, MTOPS and the use of 5ARIs: a Canadian consensus regarding implications for clinical practice
- Dutasteride, a novel dual 5-A reductase inhibitor, reduces serum DHT to a greater extent versus finasteride and achieves finasteride maximal reduction in a larger proportion of patients