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Research 271–300 of 696
- The Parathyroid Hormone Second Receptor PTH2R and its Ligand Tuberoinfundibular Peptide of 39 Residues TIP39 Regulate Intracellular Calcium and Influence Keratinocyte Differentiation
- Transcriptomic landscape of early hair follicle and epidermal development
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- YAP/TAZ Signalling Controls Epidermal Keratinocyte Fate
- Gene network analysis reveals candidate genes related with the hair follicle development in sheep
- Assessing protein sequencing in human single hair shafts of decreasing lengths
- Conditional Knockout in Mice Reveals the Critical Roles of Ppp2ca in Epidermis Development
- Keratins: Dynamic, flexible structural proteins of epithelial cells
- Identification of the C-terminal tail domain of AHF/trichohyalin as the critical site for modulation of the keratin filamentous meshwork in the keratinocyte
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Human iPS Cell-Derived Cell Aggregates Exhibited Dermal Papilla Cell Properties in in vitro Three-Dimensional Assemblage Mimicking Hair Follicle Structures
- Transcriptome Analysis Reveals Skin Lipid Metabolism Related to Wool Diameter in Sheep
- The epidermal growth factor receptor decreases Stathmin 1 and triggers catagen entry in the mouse
- Regulation of cashmere fineness traits by noncoding RNA in Jiangnan cashmere goats
- Targeting the Hippo/YAP/TAZ signalling pathway: Novel opportunities for therapeutic interventions into skin cancers
- Autophagy protects murine preputial glands against premature aging, and controls their sebum phospholipid and pheromone profile
- Genetic Control/Involvement in Hair Fiber Traits
- Ovine KRT81 Variants and Their Influence on Selected Wool Traits of Commercial Value
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Epidermolysis Bullosa Simplex Keratinocytes Show Disturbed Mitochondrial Positioning and Activity
- The Enrichment of Specific Hair Follicle-Associated Cell Populations in Plucked Hairs Offers an Opportunity to Study Gene Expression Underlying Hair Traits
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Generation of iPS-derived model cells for analyses of hair shaft differentiation
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- Mediator 1 ablation induces enamel-to-hair lineage conversion in mice through enhancer dynamics
- Vitamin D receptor cross-talk with p63 signaling promotes epidermal cell fate
- Keratin 79 is a PPARA target that is highly expressed by liver damage
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis