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Research 91–120 of 1000+
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Beyond Expectations
- Keratins and skin disease
- Significance of stress keratin expression in normal and diseased epithelia
- Endocrine controls of primary adult human stem cell biology: Thyroid hormones stimulate keratin 15 expression, apoptosis, and differentiation in human hair follicle epithelial stem cells in situ and in vitro
- Hair Keratins and Hair Follicle–Specific Epithelial Keratins
- The expression of equine keratins K42 and K124 is restricted to the hoof epidermal lamellae of Equus caballus
- Resolution of the plantar hyperkeratosis of pachyonychia congenita during chemotherapy for Ewing sarcoma
- A Novel Epithelial Keratin, hK6irs1, is Expressed Differentially in All Layers of the Inner Root Sheath, Including Specialized Huxley Cells (Flügelzellen) of the Human Hair Follicle
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Tcf3 and Lef1 regulate lineage differentiation of multipotent stem cells in skin
- Keratins of the Human Hair Follicle
- Hair follicle differentiation and regulation.
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Selenoproteins Are Essential for Proper Keratinocyte Function and Skin Development
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- The Type I Keratin 19 Possesses Distinct and Context-dependent Assembly Properties
- Vibrissa hair bulge houses two populations of skin epithelial stem cells distinct by their keratin profile
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- Congenital hair loss disorders: Rare, but not too rare
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Against the Rules: Human Keratin K80
- The extraction and characterization of human nail keratin
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- A novel human type I hair keratin gene: evidence for two keratin hHa3 isoforms
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis