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Research 31–60 of 1000+
- Benzo[<i>c</i>]quinolizin-3-ones: A Novel Class of Potent and Selective Nonsteroidal Inhibitors of Human Steroid 5α-Reductase 1
- Urinary steroids in women with androgenic alopecia
- Baiting Proteins with C<sub>60</sub>
- New 5?-reductase inhibitors: In vitro and in vivo effects
- Recent advances in oxasteroids chemistry
- 5α-Reductase inhibitors, antiviral and anti-tumor activities of some steroidal cyanopyridinone derivatives
- Recent Advances in Drug Design and Drug Discovery for Androgen- Dependent Diseases
- Anti-androgenic curcumin analogues as steroid 5-alpha reductase inhibitors
- Synthesis and in Vitro Evaluation of 4-Substituted N-(1,1-Dimethylethyl)-3-oxo-4-androstene-17.beta.-carboxamides as 5.alpha.-Reductase Inhibitors and Antiandrogens
- Maternal androgen excess inhibits fetal cardiomyocytes proliferation through RB-mediated cell cycle arrest and induces cardiac hypertrophy in adulthood
- Sex hormones and related compounds, including hormonal contraceptives
- Menopause - Andropause - Anti-Aging 2008, 11.-13. Dezember 2008, Wien - Abstracts
- Rat steroid 5α-reductase kinetic characteristics: Extreme pH-dependency of the type II isozyme in prostate and epididymis homogenates
- 11α-Hydroxyprogesterone, a potent 11β-hydroxysteroid dehydrogenase inhibitor, is metabolised by steroid-5α-reductase and cytochrome P450 17α-hydroxylase/17,20-lyase to produce C11α-derivatives of 21-deoxycortisol and 11-hydroxyandrostenedione in vitro
- Exploring the Drug Repurposing Versatility of Valproic Acid as a Multifunctional Regulator of Innate and Adaptive Immune Cells
- Androgen receptor modulators: a review of recent patents and reports (2012-2018)
- Phytochemical studies on traditional herbal medicines based on the ethnopharmacological information obtained by field studies
- Steroid Hormones
- Phytochemistry and pharmacological studies of Plumbago zeylanica L.: a medicinal plant review
- A potential review of its traditional uses, Phytochemistry, pharmacology, and toxicity of Plumbago zeylanica
- HDL as Therapeutic Tools
- Surface modification and endothelialization of biomaterials as potential scaffolds for vascular tissue engineering applications
- Is dehydroepiandrosterone a hormone?
- Inhibition of skin 5α-reductase by oral contraceptive progestins<i>in vitro</i>
- Steroidal 5α-reductase and 17α-hydroxylase/17,20-lyase (CYP17) inhibitors useful in the treatment of prostatic diseases
- Idiopathic Hirsutism*
- PLASMA C19 STEROID SULPHATE LEVELS AND INDICES OF ANDROGEN BIOAVAILABILITY IN FEMALE PATTERN ANDROGENIC ALOPECIA
- 12 Treatment of hirsutism with 5α-reductase inhibitors
- Revisiting hyper- and hypo-androgenism by tandem mass spectrometry
- Androgen antagonists in androgen target tissues