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Research 541–570 of 1000+
- Identification of a novel<i>PNPLA1</i>mutation in a Spanish family with autosomal recessive congenital ichthyosis
- PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- Secretory phospholipase A2-IIA overexpressing mice exhibit cyclic alopecia mediated through aberrant hair shaft differentiation and impaired wound healing response
- Bacteria induce skin regeneration via IL-1β signaling
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Ultraviolet Radiation in Wound Care: Sterilization and Stimulation
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis
- The Dynamics of the Skin’s Immune System
- A human vitamin D receptor mutation causes rickets and impaired Th1/Th17 responses
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Acne-Associated Syndromes
- Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods”
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Cepharanthine: a review of the antiviral potential of a Japanese-approved alopecia drug in COVID-19
- Wnt Signaling in Skin Development, Homeostasis, and Disease
- Hair Today
- FOXO1, TGF-β Regulation and Wound Healing
- Mechanisms of Disease: selective inhibition of 11β-hydroxysteroid dehydrogenase type 1 as a novel treatment for the metabolic syndrome
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- Alopecia areata
- The Role of Extracellular Vesicles in Cutaneous Remodeling and Hair Follicle Dynamics
- Pre-clinical non-viral vectors exploited for<i>in vivo</i>CRISPR/Cas9 gene editing: an overview
- A prostaglandind-synthase-positive mast cell gradient characterizes scalp patterning
- Epidermal abnormalities and increased malignancy of skin tumors in human epidermal keratin 8‐expressing transgenic mice
- Mammalian Fetal Organ Regeneration