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Research 181–210 of 1000+
- Disorders of the skin appendages
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- A 3-Year-Old Girl with Thin Hair
- The biology and genetics of curly hair
- 892 Behavior of the two circulating androgens testosterone and DHEA and their main intracellular metabolites in an androgen-sensitive sebocyte cell line
- The molecular pathogenesis of Trichilemmal carcinoma
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- A Review on Formulation and Evaluation of Shampoo
- Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency
- Suprabasal Desmoglein 3 Expression in the Epidermis of Transgenic Mice Results in Hyperproliferation and Abnormal Differentiation
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- CtBP1 Overexpression in Keratinocytes Perturbs Skin Homeostasis
- Systemic subchronic toxicity and comparison of four selenium nutritional supplements by 90-day oral exposure in Sprague-Dawley rats
- Loose anagen syndrome in one identical twin girl
- Impaired Notch‐MKP‐1 signalling in hidradenitis suppurativa: an approach to pathogenesis by evidence from translational biology
- Impaired wound healing in transgenic mice overexpressing the activin antagonist follistatin in the epidermis
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Lymphotoxin-β regulates periderm differentiation during embryonic skin development
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Alopecia and Thyroid Disease
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- The involvement of Elf5 in regulating keratinocyte proliferation and differentiation processes in skin
- <i>WNT10A</i> , dermatology and dentistry
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages