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Research 31–60 of 1000+
- The synergistic effect of phototherapy and active substances on hair growth
- Key targets of hormonal treatment of prostate cancer. Part 2: the androgen receptor and 5α-reductase
- Topical Finasteride Therapy in Hirsutism
- Synthesis and Pharmacological Evaluation of New Progesterone Esters as 5.ALPHA.-Reductase Inhibitors
- DHT and E2 synthesis-related proteins and receptors expression in male yak skin during different hair follicle stages
- Synthesis of phenanthridin-3-one derivatives: Non-steroidal inhibitors of steroid 5-α-reductase
- The Dark Side of 5α-Reductase Inhibitors' Therapy: Sexual Dysfunction, High Gleason Grade Prostate Cancer and Depression
- 12 Treatment of hirsutism with 5α-reductase inhibitors
- Intratumoral <i>De Novo</i> Steroid Synthesis Activates Androgen Receptor in Castration-Resistant Prostate Cancer and Is Upregulated by Treatment with CYP17A1 Inhibitors
- 5α-Reductase Inhibitors, Chemical and Clinical Models
- 5α- Reductase Inhibitors in Prostate Cancer: An Overview
- The dihydrotestosterone (DHT) hypothesis of prostate cancer and its therapeutic implications
- Reduced estradiol synthesis by letrozole, an aromatase inhibitor, is protective against development of pentylenetetrazole-induced kindling in mice
- Novel inhibitors of 5α-reductase
- FCE 28260, a new 5α-reductase inhibitor: In vitro and in vivo effects
- Pharmacophore and Atom Based 3D QSAR Studies on the Novel 5-Alpha-Reductase Inhibitors
- Nonsteroidal inhibitors of human type I steroid 5-.alpha.-reductase
- Maternal androgen excess inhibits fetal cardiomyocytes proliferation through RB-mediated cell cycle arrest and induces cardiac hypertrophy in adulthood
- Sex steroid synthesis in human skin in situ: The roles of aromatase and steroidogenic acute regulatory protein in the homeostasis of human skin
- Discovery of Natural Steroid 5 Alpha-Reductase Inhibitors
- Novel type 1 5a-reductase Inhibitors with Antiproliferative Potential on LNCaP cells
- Synthesis and biological evaluation of esters of 16-formyl-17-methoxy-dehydroepiandrosterone derivatives as inhibitors of 5α-reductase type 2
- Molecular docking simulation studies on potent butyrylcholinesterase inhibitors obtained from microbial transformation of dihydrotestosterone
- DIHYDROTESTOSTERONE AND THE PROSTATE: THE SCIENTIFIC RATIONALE FOR 5α-REDUCTASE INHIBITORS IN THE TREATMENT OF BENIGN PROSTATIC HYPERPLASIA
- Simultaneous pharmacokinetic and pharmacodynamic analysis of 5α-reductase inhibitors and androgens by liquid chromatography tandem mass spectrometry
- Aromatase-independent testosterone conversion into estrogenic steroids is inhibited by a 5α-reductase inhibitor
- Steroid 5α-Reductase Inhibitors
- Chapter 23. Therapeutic Control of Androgen Action
- An overview on 5α-reductase inhibitors
- 9 Role of 5α-reductase in health and disease