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Research 181–210 of 1000+
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Pelvic ultrasound and color Doppler findings in different isosexual precocities
- LY191704: a selective, nonsteroidal inhibitor of human steroid 5 alpha-reductase type 1.
- Gender aspects in skin diseases
- Risk Factors and Characterization of Vitiligo and Alopecia Areata in Patients With Chronic Graft-vs-Host Disease
- Effects of pre- and post-pubertal dihydrotestosterone treatment on penile length in 5α-reductase type 2 deficiency
- An Asian traditional herbal complex containing Houttuynia cordata Thunb, Perilla frutescens Var. acuta and green tea stimulates hair growth in mice
- 46, XY 5-Alpha Reductase Deficiency in a 36-Year-Old Phenotypic Female Patient
- Clinical Trials and Hair Loss
- Clinical characteristics and risk factors of female precocious puberty
- Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty
- Steroid Sulfatase in the Human Hair Follicle Concentrates in the Dermal Papilla
- Pregnancy and the Skin
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- Modelling androgen synthesis and action during human sexual differentiation
- Pharmacology of anabolic steroids
- Physiological and biological skin changes in pregnancy
- Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization)
- Recent Advances in Drug Design and Drug Discovery for Androgen- Dependent Diseases
- Predominant expression of 5 alpha-reductase type 1 in pubic skin from normal subjects and hirsute patients.
- Assessment, Treatment, and Prevention Strategies for Hair-Thread Tourniquet Syndrome in Infants
- Raising awareness of Demodex mites: a neglected cause of skin disease
- Dutasteride: A Review of its Use in the Management of Prostate Disorders
- Dermatologia e Procedimentos Estéticos Ed. XXVII
- Estrogen and androgen signaling in the pathogenesis of BPH
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- INTERFERONS IN DERMATOLOGY
- Frontal fibrosing alopecia and lichen planopilaris in HLA-identical mother and daughter