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Research 691–720 of 1000+
- Current Guidelines for Diagnosing PCOS
- Macrophage Related Chronic Inflammation in Non-Healing Wounds
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair
- Single-cell RNA-seq highlights heterogeneity in human primary Wharton’s jelly mesenchymal stem/stromal cells cultured in vitro
- Male pseudohermaphroditism due to 17β-hydroxysteroid dehydrogenase deficiency: Studies on the natural history of the defect and effect of androgens on gender role
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Understanding the role of prostaglandin E2 in regulating human platelet activity in health and disease
- A comparison of transcriptomic patterns measured in the skin of Chinese fine and coarse wool sheep breeds
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit
- Ectodysplasin Signaling in Cutaneous Appendage Development: Dose, Duration, and Diversity
- Making the head: Caspases in life and death
- Triglycerides, independent of Ferriman Gallwey Score, is a main determinant of free testosterone index in PCOS
- GWASs Identify Genetic Loci Associated with Human Scalp Hair Whorl Direction
- A New Universal Follicular Unit Excision Classification System for Hair Transplantation Difficulty and Patient Outcome
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep
- Expansion Culture of Hair Follicle Stem Cells through Uniform Aggregation in Microwell Array Devices
- A Short Report on Melanocyte/Melanoma Culture, Senescence, and Reproducibility
- Approach to the Patient: Diagnostic Challenges in the Work Up for Polycystic Ovary Syndrome
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- From bench to babies – drug development for male subfertility
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- POLİKİSTİK OVER SENDROMU'NUN ALT GRUPLARINDA METABOLİK ÖZELLİKLER
- Editor's evaluation: Involvement of ILC1-like innate lymphocytes in human autoimmunity, lessons from alopecia areata
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus: Is nomenclature “porokeratotic adnexal ostial nevus” more appropriate?
- Keratin K15 as a Biomarker of Epidermal Stem Cells
- Endogenous/exogenous stimuli‐responsive smart hydrogels for diabetic wound healing
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation