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Research 391–420 of 1000+
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Human hair keratin and its-based biomaterials for biomedical applications
- The effect of human hair keratin hydrogel on early cellular response to sciatic nerve injury in a rat model
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Regulation of Keratin 9 in Nonpalmoplantar Keratinocytes by Palmoplantar Fibroblasts Through Epithelial–Mesenchymal Interactions
- Keratin 16 Expression Defines a Subset of Epithelial Cells During Skin Morphogenesis and the Hair Cycle
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Alkylation of human hair keratin for tunable hydrogel erosion and drug delivery in tissue engineering applications
- Preparation and characterization of keratin-based biocomposite hydrogels prepared by electron beam irradiation
- Keratin 17 Gene Expression during the Murine Hair Cycle
- Angora Mouse Mutation: Altered Hair Cycle, Follicular Dystrophy, Phenotypic Maintenance of Skin Grafts, and Changes in Keratin Expression
- Efficient In Vivo Targeting of Epidermal Stem Cells by Early Gestational Intraamniotic Injection of Lentiviral Vector Driven by the Keratin 5 Promoter
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Changing the shape of hair with keratin peptides
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- Keratins 1 and 10 or homologues as regular constituents of inner root sheath and cuticle cells in the human hair follicle.
- Keratin network modifications lead to the mechanical stiffening of the hair follicle fiber
- Cloning of human, murine, and marsupial keratin 7 and a survey of K7 expression in the mouse
- 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
- Damage of hair follicle stem cells and alteration of keratin expression in external radiation-induced acute alopecia
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Thyroxine (T4) may promote re-epithelialisation and angiogenesis in wounded human skin ex vivo
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11
- Transient expression of keratin 19 is induced in originally negative interfollicular epidermal cells by adhesion of suspended cells.
- The Proteins of Normal and Aberrant Hair Keratins
- Hard Keratin IF and Associated Proteins