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Research 661–690 of 1000+
- Toward understanding scarless skin wound healing and pathological scarring
- Aging of the hair follicle pigmentation system
- Lineage Analysis of Epidermal Stem Cells
- Embryonic hair follicle fate change by augmented β-catenin through Shh and Bmp signaling
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Trichoscopy (hair and scalp videodermoscopy) in the healthy female. Method standardization and norms for measurable parameters
- Deciphering the Complex Immunopathogenesis of Alopecia Areata
- Poliosis circumscripta: Overview and underlying causes
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- <i>NUDT15</i>,<i>FTO</i>, and<i>RUNX1</i>genetic variants and thiopurine intolerance among Japanese patients with inflammatory bowel diseases
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Frontal fibrosing alopecia: An update on the hypothesis of pathogenesis and treatment
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- Central Centrifugal Cicatricial Alopecia: New Insights and a Call for Action
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- Human Hair Graying Revisited: Principles, Misconceptions, and Key Research Frontiers
- New approach to the understanding of keloid: psychoneuroimmune–endocrine aspects
- A Comprehensive Review of Mammalian Pigmentation: Paving the Way for Innovative Hair Colour-Changing Cosmetics
- Rare Germline Pathogenic Variants Identified by Multigene Panel Testing and the Risk of Aggressive Prostate Cancer
- Are sex hormones promising candidates to explain sex disparities in the COVID-19 pandemic?
- What′s new in cicatricial alopecia?
- Alopecia areata - Vitiligo overlap syndrome: An emerging clinical variant
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Fertility counseling and preservation: considerations for the pediatric endocrinologist
- Synthetically programmed antioxidant delivery by a domesticated skin commensal
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)