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Research 481–510 of 1000+
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- Premature aging syndromes: From patients to mechanism
- The Genetic Architecture of Alopecia Areata
- Murine Epidermal Ceramide Synthase 4 Is a Key Regulator of Skin Barrier Homeostasis
- Stress-sensing in the human greying hair follicle: Ataxia Telangiectasia Mutated (ATM) depletion in hair bulb melanocytes in canities-prone scalp
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- The Immunological Impact of IL-1 Family Cytokines on the Epidermal Barrier
- Society for Endocrinology Clinical Practice Guideline for the Evaluation of Androgen Excess in Women
- TRP Channels in Skin Biology and Pathophysiology
- Pharmacologic interventions in aging hair
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- The Role of Sex and Gender in Dermatology - From Pathogenesis to Clinical Implications
- Sex-limited chromosomes and non-reproductive traits
- Prostaglandins: Key players in immunomodulation of the nervous system
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Synopsis: 2005 Annual Meeting of the American Society of Andrology
- From Follicle Cell Differentiation and Structure to Chorion Biogenesis in Insects: Cellular Mechanisms, Gene Regulation, Biochemical Composition and Structural Diversity
- JAK-Inhibitors Beyond the Label: Emerging Applications in Dermatology
- Technological Advances in Anti-hair Loss and Hair Regrowth Cosmeceuticals: Mechanistic Breakthroughs and Industrial Prospects Driven by Multidisciplinary Collaborative Innovation
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- The importance of basonuclin 2 in adult mice and its relation to basonuclin 1
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- Clinical and molecular genetic studies in hereditary hair loss
- Esclerodermia localizada semelhante à morféia em um gato
- Abnormal fingerprints and immigration delay disease
- Localized Acquired Hypertrichosis Associated with the Application of a Splint
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- Banded Scalp Hair with an Unusual Glistening Appearance in a Teenager: A Quiz
- Familial congenital generalized hypertrichosis
- Acquired progressive kinking of hair affecting the scalp and eyelashes in an adult woman