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Research 601–630 of 1000+
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- Characterisation of Four New Genes in the Ovine KAP19 Family
- Trends in biopolymer science applied to cosmetics
- Keratinization and its Disorders
- Keratohyalin, Trichohyalin and Keratohyalin‐Trichohyalin Hybrid Granules: An Overview
- Thyroid-Stimulating Hormone, a Novel, Locally Produced Modulator of Human Epidermal Functions, Is Regulated by Thyrotropin-Releasing Hormone and Thyroid Hormones
- Nestin is a marker of unipotent embryonic and adult progenitors differentiating into an epithelial cell lineage of the hair follicles
- Nestin as a marker of unipotent epithelial progenitor cells differentiate into outer root sheath keratinocytes in embryonic and adult hair follicles
- Proteomic Analysis of Single Hairs
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Science and Technology of Hair Fibers
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- <i>Igf1r</i> signalling acts on the anagen‐to‐catagen transition in the hair cycle
- Clinical Snippets
- Reply to: The ends of a conundrum?
- From molecular biology to therapeutics
- Data from Mobilizing Transit-Amplifying Cell-Derived Ectopic Progenitors Prevents Hair Loss from Chemotherapy or Radiation Therapy
- The Effects of Spermidine on Functional and Transcriptomic Markers in Human Primary Keratinocytes
- Structural and Immunocytochemical Characterization of Keratinization in Vertebrate Epidermis and Epidermal Derivatives
- The role of cathepsin E in terminal differentiation of keratinocytes
- Structure and expression of the ovine Hoxc-13 gene
- Meta-Analysis of Gene Expression Reveals the Core Transcriptomic Profile of Lesional Scalp in Alopecia Areata
- Reinforcing chemically treated human hair with citric acid
- Cross‐linked features of mouse pelage hair resistant to detergent extraction
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle
- Epidermal structure created by canine hair follicle keratinocytes enriched with bulge cells in a three‐dimensional skin equivalent model <i>in vitro</i>: implications for regenerative therapy of canine epidermis
- Epithelial loss of mitochondrial oxidative phosphorylation leads to disturbed enamel and impaired dentin matrix formation in postnatal developed mouse incisor
- Single-Cell Proteomics Uncovers Dual Traits of Dermal Sheath Cells in Wound Repair