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Research 331–360 of 564
- Divergent roles of HDAC1 and HDAC2 in the regulation of epidermal development and tumorigenesis
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Comparative Anatomy of Mouse and Human Nail Units
- Proliferative and Non-Proliferative Lesions of the Rat and Mouse Integument
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Structure and Mechanical Properties of Human Trichocyte Keratin Intermediate Filament Protein
- Specific morphogenetic events in mouse external genitalia sex differentiation are responsive/dependent upon androgens and/or estrogens
- Distinct mechanisms for sebaceous gland self-renewal and regeneration provide durability in response to injury
- The structure of the cornified claw sheath in the domesticated cat (<i>Felis catus</i>): implications for the claw‐shedding mechanism and the evolution of cornified digital end organs
- Estrogen Leads to Reversible Hair Cycle Retardation through Inducing Premature Catagen and Maintaining Telogen
- Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty
- Characterization of Hair Follicle Development in Engineered Skin Substitutes
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Viral-Associated Trichodysplasia of Immunosuppression
- Integrated Analysis of Methylome and Transcriptome Changes Reveals the Underlying Regulatory Signatures Driving Curly Wool Transformation in Chinese Zhongwei Goats
- Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency
- Deciphering the functions of the hair follicle infundibulum in skin physiology and disease
- Expression patterns of programmed cell death 4 protein in normal human skin and some representative skin lesions
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- Natural Sources of Therapeutic Agents Used in Skin Conditions
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- Loss of Keratin K2 Expression Causes Aberrant Aggregation of K10, Hyperkeratosis, and Inflammation
- Chronic graft versus host disease and skin
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- Transglutaminase-3 Enzyme: A Putative Actor in Human Hair Shaft Scaffolding?
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.