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Research 31–60 of 1000+
- Structural Transition of Trichocyte Keratin Intermediate Filaments During Development in the Hair Follicle
- A Unique Type I Keratin Intermediate Filament Gene Family is Abundantly Expressed in the Inner Root Sheaths of Sheep and Human Hair Follicles
- Characterization of a Hair (Wool) Keratin Intermediate Filament Gene Domain
- Role of human type II hair keratins in intermediate filament bundling in vitro
- Complete Structure of an Epithelial Keratin Dimer: Implications for Intermediate Filament Assembly
- Cornification in reptilian epidermis occurs through the deposition of keratin‐associated beta‐proteins (beta‐keratins) onto a scaffold of intermediate filament keratins
- BMP4 and nuclear laminC orchestrate a expression of AHF/Trichohyalin molecule, a key modulator of keratin intermediate filaments in the hair follicle
- The structure of human trichohyalin. Potential multiple roles as a functional EF-hand-like calcium-binding protein, a cornified cell envelope precursor, and an intermediate filament-associated (cross-linking) protein
- The role of disulfide bond formation in the structural transition observed in the intermediate filaments of developing hair
- Isolation of intermediate filament assemblies from human hair follicles.
- From structural resilience to cell specification — Intermediate filaments as regulators of cell fate
- Existence of trichohyalin-keratohyalin hybrid granules: Co-localization of two major intermediate filament-associated proteins in non-follicular epithelia
- Unzipping the cuticle of the human hair shaft to obtain micron/nano keratin filaments
- A general mathematical model for the in vitro assembly dynamics of intermediate filament proteins
- Genes for intermediate filament proteins and the draft sequence of the human genome
- Disulfide Cross-Linked Network Structure of Intermediate Filament and Matrix in Hair and Wool Cortices
- Structural changes in the trichocyte intermediate filaments accompanying the transition from the reduced to the oxidized form
- Cyclic hair-loss and regrowth in transgenic mice overexpressing an intermediate filament gene.
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Human Hair Keratin-Associated Proteins
- Keratins and skin disease
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- The keratins and their disorders
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Effect of varied hair protein fractions on the gel properties of keratin/chitosan hydrogels for the use in tissue engineering
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Keratins: Dynamic, flexible structural proteins of epithelial cells