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- Determination of rat 5α-reductase type 1 isozyme activity and its inhibition by novel steroidal oxazolines
- LY191704: a selective, nonsteroidal inhibitor of human steroid 5 alpha-reductase type 1.
- Immunolocalization of 5α-Reductase Isozymes in Acne Lesions and Normal Skin
- Human Osteoblast-Like Cells Express Predominantly Steroid 5α-Reductase Type 1
- mRNA Levels of Aromatase, 5α-Reductase Isozymes, and Prostate Cancer-Related Genes in Plucked Hair from Young Men with Androgenic Alopecia
- Synthesis and Biological Evaluation of 4-(4-(Alkyl-and Phenylaminocarbonyl)benzoyl)benzoic Acid Derivatives as Non-steroidal Inhibitors of Steroid 5α-Reductase Isozymes 1 and 2
- 5 Alpha-reductase inhibitors: whatʼs new?
- Recent Advances in Drug Design and Drug Discovery for Androgen- Dependent Diseases
- The 5α-Recluctase System and Its Inhibitors
- Synthesis of phenanthridin-3-one derivatives: Non-steroidal inhibitors of steroid 5-α-reductase
- Inhibitory Effects of Serenoa repens on the Kinetic of Pig Prostatic Microsomal 5α-Reductase Activity
- Sponsored Lecture 3 : Updates on 5 alpha-rers(5ARIs) for the treatment of male pattern hair loss(MPHL)
- Slow progress in prostate cancer
- Activity of type 1 5α-reductase is greater in the follicular infrainfundibulum compared with the epidermis
- Selective non-steroidal inhibitors of 5α-reductase type 1
- Immunohistochemical localization of types 1 and 2 5α-reductase in human scalp
- 5α-reductase activity in the prostate
- Benzo[<i>c</i>]quinolizin-3-ones: A Novel Class of Potent and Selective Nonsteroidal Inhibitors of Human Steroid 5α-Reductase 1
- Molecular interactions of progesterone derivatives with 5α-reductase types 1 and 2 and androgen receptors
- Novel 5α-Reductase Inhibitors: Synthesis, Structure−Activity Studies, and Pharmacokinetic Profile of Phenoxybenzoylphenyl Acetic Acids
- Hypersensitivity Reactions to Anticoagulant Drugs
- FCE 28260, a new 5α-reductase inhibitor: In vitro and in vivo effects
- Synthesis and Evaluation of 2‘-Substituted 4-(4‘-Carboxy- or 4‘-carboxymethylbenzylidene)-<i>N</i>-acylpiperidines: Highly Potent and in Vivo Active Steroid 5α-Reductase Type 2 Inhibitors
- 5α-reductase isoenzymes mediate stress-exacerbated Tourette-like responses in animal models
- The Rationale for Inhibiting 5α-Reductase Isoenzymes in the Prevention and Treatment of Prostate Cancer
- Dihydrotestosterone and the Concept of 5α–Reductase Inhibition in Human Benign Prostatic Hyperplasia
- 5α-Reductase Inhibitors, Chemical and Clinical Models
- Mechanism of action of herbs and their active constituents used in hair loss treatment
- Comparison of clinical trials with finasteride and dutasteride.
- Dutasteride in Androgenetic Alopecia: An Update