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Research 781–810 of 1000+
- Regulation of Epidermal Ferritin Expression Influences Systemic Iron Homeostasis
- Expression of mineralized tissue associated proteins: Dentin sialoprotein and phosphophoryn in rodent hair follicles
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Isolation of Multipotent Nestin-Expressing Stem Cells Derived from the Epidermis of Elderly Humans and TAT-VHL Peptide-Mediated Neuronal Differentiation of These Cells
- Bulge-Derived Epithelial Cells Isolated from Human Hair Follicles Using Enzymatic Digestion or Explants Result in Comparable Tissue-Engineered Skin
- Suprabasal Desmoglein 3 Expression in the Epidermis of Transgenic Mice Results in Hyperproliferation and Abnormal Differentiation
- Skin-specific expression of a truncated E1a oncoprotein binding to p105-Rb leads to abnormal hair follicle maturation without increased epidermal proliferation.
- Differential expression of stem cell markers in human follicular bulge and interfollicular epidermal compartments
- Slug (Snai2) Expression during Skin and Hair Follicle Development
- Advances in molecular pathogenesis of hidradenitis suppurativa: Dysregulated keratins and ECM signaling
- <i>egfl6</i> expression in the pharyngeal pouch is dispensable for craniofacial development
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- A Review of Keratin-Based Biomaterials for Biomedical Applications
- Keratins and skin disease
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair
- Studies on the Proteome of Human Hair - Identification of Histones and Deamidated Keratins
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Microarray analysis of androgenetic and senescent alopecia: Comparison of gene expression shows two distinct profiles
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Selective Expression of Calcium-Binding Proteins S100A8 and S100A9 at Distinct Sites of Hair Follicles
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Altered FGF expression profile in human scalp-derived fibroblasts upon WNT activation: implication of their role to provide folliculogenetic microenvironment
- Recent advances in preparation and biomedical applications of keratin based biomaterials
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Methods of keratin extraction from wool and hair and prospects of their application in biomedicine and bioengineering
- Keratin biomaterials for wound healing and tissue regeneration: A promising approach in biomedical applications
- Comprehensive characterization of keratin extracted from patients with androgenetic alopecia and healthy individuals through multimolecular spectroscopy and structural analysis
- Tenascin expression in normal human adult skin and skin appendage tumours