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Research 31–60 of 69
- Secondary cicatricial and other permanent alopecias
- Diagnosis of common, benign neonatal dermatoses
- The Spectrum of Skin Disease Among Indian Children
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Differential expression and functionality of ATP-binding cassette transporters in the human hair follicle
- The Genetics of Human Skin Disease
- Immunological control of skin development: from homeostasis to developmental pathologies
- Table of Contents
- Drug Discovery Today: Therapeutic Strategies - 2006 Editorial
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Off-label uses of retinoids in dermatology
- “Structural imprinting” of the cutaneous immune effector function
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Type XVII collagen coordinates proliferation in the interfollicular epidermis
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Navaratnas in Dermatology
- Role of the ABCA4 Gene Expression in the Clearance of Toxic Vitamin A Derivatives in Human Hair Follicle Stem Cells and Keratinocytes
- Alopecia in Harlequin mutant mice is associated with reduced AIF protein levels and expression of retroviral elements
- Beyond Appearances: The Hidden Coat Diversity of the Sicilian Mastiff Revealed by Integrated Phenotypic and Genetic Analyses
- Smoker’s Mustache Revisited: Upper Lip Hair Yellow Discoloration Associated With Tobacco
- Unilateral Straight Hair—A Symptom of Acquired Horner's Syndrome in a Neonate
- To study the prevalence of cutaneous manifestationsin newborns and its correlation with defined maternal and neonatal factors
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- Ptosis in childhood