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Research 451–480 of 1000+
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- FC‐10 Adult‐onset hair loss in Chesapeake Bay retrievers: a clinical and histological study
- Spironolactone versus Bicalutamide for Female Pattern Hair Loss: A 24-Month Unicenter Retrospective Comparative Study of Effectiveness and Safety
- Australasian Society for Dermatology Research Meeting, May 2006
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- Effect of shampoo, conditioner and permanent waving on the molecular structure of human hair
- A Narrative Review of Advances in Skin Tissue Engineering: From Physiological Architecture to 3D Bioprinting
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Murine Vibrissae Cultured in Serum-Free Medium Reinitiate Anagen
- Non-scarring alopecia in systemic lupus erythematosus patients at the Lagos State University Teaching Hospital: a cross-sectional study of prevalence, pattern, trichoscopy features and histopathological analysis
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Telogen Effluvium
- An overview on congenital alopecia in domestic animals
- Mutant Cx43 in Skin Differentiation and Disease
- What causes acne inversa (or hidradenitis suppurativa)? – The debate continues
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- CtBP1 Overexpression in Keratinocytes Perturbs Skin Homeostasis
- Telogen Effluvium: A Review
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Overexpression of Smad7 results in severe pathological alterations in multiple epithelial tissues
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- [Netherton's syndrome in two sisters].
- A case of congenital pili multigemini
- Alopecia in IL-10-deficient mouse pups is c-kit-dependent and can be triggered by iron deficiency
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel