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Research 931–960 of 1000+
- The endocrinology of baldness
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- Perspectives in dermatopathology: telomeres and telomerase in ageing and cancer; with emphasis on cutaneous disease
- Evolving approaches to profiling the microbiome in skin disease
- Common Baldness in Women
- Physiology and Medical Treatments for Alopecia
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Infertility: Evaluation and Initial Management
- Nonscarring hair loss disorders
- Interventions for androgenic alopecia in women
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Correlation between sebum level and severity of male androgenetic alopecia
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Development of polycystic ovary syndrome: involvement of genetic and environmental factors
- Hair Depigmentation Is a Biological Readout for Pharmacological Inhibition of KIT in Mice and Humans
- Loose anagen hair syndrome in children of Upper Egypt
- A Child with Nonscarring Alopecia
- Analisis IMT Terhadap Alopesia Androgenik Fakultas Kedokteran, RS Ibnu Sina Dan Menara UMI Makassar
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Follikelhormone
- Polycystic Ovary Syndrome in Adolescents
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Establishment of Tsc2-deficient rat embryonic stem cells
- Hair cross-sectioning in uncombable hair syndrome: An easy tool for complex diagnosis
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Long-Term Effects of Sirolimus on Human Skin TSC2-Null Fibroblast‒Like Cells
- Clinico-epidemiology of Keratosis Pilaris with Histopathologic and Dermoscopic Evaluation – A Cross-sectional Study in a Rural Tertiary Hospital