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Research 271–300 of 725
- Skin, Genetic Defects, and Aging
- The ATP sensitive potassium channel (KATP) is a novel target for migraine drug development
- Keratin 15 Expression in Stratified Epithelia: Downregulation in Activated Keratinocytes
- Combined drug triads for synergic neuroprotection in retinal degeneration
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- The molecular basis of human keratin disorders
- Normalization of hair growth in sparse fur-abnormal skin and hair (SPF-ASH) mice by introduction of the rat ornithine transcarbamylase (OTC) gene
- 3α-androstanediol, but not testosterone, attenuates age-related decrements in cognitive, anxiety, and depressive behavior of male rats
- Mineral Malnutrition Following Bariatric Surgery
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Long-Term Survival of Type XVII Collagen Revertant Cells in an Animal Model of Revertant Cell Therapy
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Pilomatricoma in the infraorbital region
- The potential application of natural products in cutaneous wound healing: A review of preclinical evidence
- Novel tip-loaded dissolving and implantable microneedle array patches for sustained release of finasteride
- Analysis of nutritional elements in Indian medicinal herbs used to cure general weakness
- The Catalog of Human Hair Keratins
- Regulation of Involucrin Gene Expression
- The Intermediate Filament Architecture as Determined by X-Ray Diffraction Modeling of Hard α-Keratin
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Synthesis of porcine pCLCA2 protein during late differentiation of keratinocytes of epidermis and hair follicle inner root sheath
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Photobiomodulation therapy
- A Hairy Cituation – PADIs in Regeneration and Alopecia
- A desmosomal cadherin controls multipotent hair follicle stem cell quiescence and orchestrates regeneration through adhesion signaling