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Research 30 of 524
- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation
- Analysis of the sheep trichohyalin gene: potential structural and calcium-binding roles of trichohyalin in the hair follicle.
- Proteopedia entry: Coiled‐coil structure of keratins
- 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
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Direct evidence supporting the existence of a helical dislocation in protofilament packing in the intermediate filaments of oxidized trichocyte keratin
- The Intermediate Filament Architecture as Determined by X-Ray Diffraction Modeling of Hard α-Keratin
- Complete Structure of an Epithelial Keratin Dimer: Implications for Intermediate Filament Assembly
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Inherited Disorders of the Hair
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- 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
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Keratin disorders: from gene to therapy
- Semidominant Inheritance in Epidermolytic Ichthyosis
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Self-consistent field theory for the interactions between keratin intermediate filaments
- Human Hair Keratin‐Associated Proteins (KAPs)
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- The susceptibility of disulfide bonds to modification in keratin fibers undergoing tensile stress
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Targeting integrin pathways: mechanisms and advances in therapy
- Intramembrane Proteolysis of Astrotactins