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Research 391–420 of 1000+
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Localized Acquired Hypertrichosis Associated with the Application of a Splint
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Recently Identified Forms of Epidermolysis Bullosa
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Biologically Driven Innovations in Aesthetic Surgery: Advances in Regenerative and Cellular Therapies
- Role of the Wnt signaling pathway in keratoacanthoma
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- Nilotinib-induced generalized keratosis pilaris: Report of a rare case
- Dynamic expression of the zinc-finger transcription factor Trps1 during hair follicle morphogenesis and cycling
- Characterization of Hydrogels of Gelatin/O-Carboxymethyl Chitosan in Ovule Form with Curcumin and Retinyl Palmitate as a Treatment for Cervical Cancer
- Primary TSC2-/meth Cells Induce Follicular Neogenesis in an Innovative TSC Mouse Model
- A Holistic Approach to Unravel Keloid Pathogenesis and Optimize Therapeutic Outcomes
- The developmental basis of fingerprint pattern formation and variation
- Pathological Skin Scarring: From Mechanism to Targeted Local Therapy
- Monilethrix: A case report imaged by trichoscopy, reflectance confocal microscopy and histopathology
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Persistent Papular Eruption in a Young Adult: Importance of Histopathology in Diagnosing Eruptive Vellus Hair Cysts
- The clinical spectrum of parathyroid disease
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function
- Roles of tumor suppressors in regulating tumor-associated inflammation
- Ashy Dermatosis
- 9. Immunology and Genetics
- Wnt Signaling in Skin Development, Homeostasis, and Disease