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Research 901–930 of 1000+
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Expression patterns of keratin intermediate filament and keratin associated protein genes in wool follicles
- Stimulation of Hair Growth by Small Molecules that Activate Autophagy
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Obesity resistance of the stearoyl-CoA desaturase-deficient (<i>scd1</i> <sup>-/-</sup>) mouse results from disruption of the epidermal lipid barrier and adaptive thermoregulation
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Metabolites from Macroalgae and Its Applications in the Cosmetic Industry: A Circular Economy Approach
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Vitiligo - Part 2 - classification, histopathology and treatment
- Trends in Prevalence and Incidence of Alopecia Areata, Alopecia Totalis, and Alopecia Universalis Among Adults and Children in a US Employer-Sponsored Insured Population
- Histologic Changes in the Skin of Hairless Mice Following Peeling With Salicylic Acid
- Progressive Alopecia Reveals Decreasing Stem Cell Activation Probability during Aging of Mice with Epidermal Deletion of DNA Methyltransferase 1
- New clinico‐genetic classification of trichothiodystrophy
- The dark art of light measurement: accurate radiometry for low-level light therapy
- Specific Citrullination Causes Assembly of a Globular S100A3 Homotetramer
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Embryonic hair follicle fate change by augmented β-catenin through Shh and Bmp signaling
- Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis
- Ultrastructural evaluation of the radioprotective effects of melatonin against X‐ray‐induced skin damage in Albino rats
- Application of Hydrogels as Three-Dimensional Bioprinting Ink for Tissue Engineering
- The Spectrum of Scarring in Craniofacial Wound Repair
- Significance of stress keratin expression in normal and diseased epithelia
- Dynamic interplay between IL-1 and WNT pathways in regulating dermal adipocyte lineage cells during skin development and wound regeneration
- Disruption of Smad4 in Mouse Epidermis Leads to Depletion of Follicle Stem Cells
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- The regenerative potential of skin and the immune system
- Discrimination of Dysplastic Nevi from Common Melanocytic Nevi by Cellular and Molecular Criteria
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production