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Research 61–90 of 536
- A girl with loose anagen hair syndrome and concurrent uncombable hair syndrome
- Intermediate Hair Follicles from Patients with Female Pattern Hair Loss Are Associated with Nutrient Insufficiency and a Quiescent Metabolic Phenotype
- Diseases of Hair
- Diseases of Hair
- Focused Review on Metal Nanoparticles in Hair Regeneration and Alopecia: Insights into Mechanisms, Assessment Techniques, Toxicity, Regulatory and Intellectual Property Perspectives
- TMT-Based Quantitative Proteomic Analysis Reveals the Effect of Bone Marrow Derived Mesenchymal Stem Cell on Hair Follicle Regeneration
- Evolution of long scalp hair in humans
- Wnt signaling modulates mechanotransduction in the epidermis to drive hair follicle regeneration
- [Nevoid bundle hairs].
- Loss of ‘Epidermal Melanin Unit’ Integrity in Human Skin During Melanoma-Genesis
- Oral Presentations
- Targeting Superficial or Nodular Basal Cell Carcinoma with Topically Formulated Small Molecule Inhibitor of Smoothened
- Trichotillomania in Children
- Scaffold-based developmental tissue engineering strategies for ectodermal organ regeneration
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- SUMMARIES OF PAPERS
- PHILADELPHIA DERMATOLOGICAL SOCIETY
- How to Speak Postmodern: Medicine, Illness, and Cultural Change
- The Spectrum of Skin Disease Among Indian Children
- Gender-Affirming Hormone Therapy for Transgender Men
- Understanding Microemulsions and Nanoemulsions in (Trans)Dermal Delivery
- Temporal Triangular Alopecia—Clinical and Dermoscopic Features of a Rare Entity
- Eyebrow Loss
- Multifunctional Injectable Hydrogel Loaded with Cerium-Containing Bioactive Glass Nanoparticles for Diabetic Wound Healing
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles