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Research 61–90 of 1000+
- Special Biochemical Features of the Hair Follicle
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Keratins: Dynamic, flexible structural proteins of epithelial cells
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- The Type I Keratin 19 Possesses Distinct and Context-dependent Assembly Properties
- Rational design of keratin nanoparticles utilizing diverse hair protein fractions for controlled drug release
- Keratins and skin disease
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Proteome Analysis of Human Hair Shaft
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Evolution of Trichocyte Keratins
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- Keratin expression by corneal and limbal stem cells during development
- Mesenchymal Stem Cells From Mouse Hair Follicles Reduce Hypertrophic Scarring in a Murine Wound Healing Model
- Transcriptome analysis reveals the genetic basis underlying the development of skin appendages and immunity in hedgehog (Atelerix albiventris)
- Sequence and expression of human hair keratin genes
- Against the Rules: Human Keratin K80
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- An Integrated Analysis of Cashmere Fineness lncRNAs in Cashmere Goats
- Bioinformatics analysis of genes associated with the patchy-type alopecia areata: CD2 may be a new therapeutic target
- Bidirectional binding property of high glycine–tyrosine keratin-associated protein contributes to the mechanical strength and shape of hair
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function
- Type I Keratin 17 Protein Is Phosphorylated on Serine 44 by p90 Ribosomal Protein S6 Kinase 1 (RSK1) in a Growth- and Stress-dependent Fashion
- Transglutaminase-3 Enzyme: A Putative Actor in Human Hair Shaft Scaffolding?
- Vibrissa hair bulge houses two populations of skin epithelial stem cells distinct by their keratin profile
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- High proliferation and delamination during skin epidermal stratification
- Epidermal abnormalities and increased malignancy of skin tumors in human epidermal keratin 8‐expressing transgenic mice
- Trichohyalin: Presence in the Granular Layer and Stratum Corneum of Normal Human Epidermis