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Research 31–60 of 1000+
- 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
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Expression of type I hair keratins in follicular tumours
- A novel human type I hair keratin gene: evidence for two keratin hHa3 isoforms
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- A cDNA encoding the human type I hair keratin hHa1
- Structure and site of expression of a murine type II hair keratin
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Sequence of a Cashmere goat type I hair keratin gene and its expression in skin
- Characterization of a 190-Kilobase Pair Domain of Human Type I Hair Keratin Genes
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Differential expression of type I IRS keratin genes in three breeds of sheep
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Detection of Type IIHair Keratin Gene in a Family with Monilethrix
- Unique amino acid signatures that are evolutionarily conserved distinguish simple-type, epidermal and hair keratins
- The Type I Keratin 19 Possesses Distinct and Context-dependent Assembly Properties
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Differential Expression of Type I Hair Keratins
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Hair-Specific Keratins: Characterization and Expression of a Mouse Type I Keratin Gene
- Role of human type II hair keratins in intermediate filament bundling in vitro
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- A Unique Type I Keratin Intermediate Filament Gene Family is Abundantly Expressed in the Inner Root Sheaths of Sheep and Human Hair Follicles
- Expression analysis of the type I keratin protein keratin 33A in goat coat hair
- Cachexia and graft-vs.-host-disease-type skin changes in keratin promoter-driven TNF alpha transgenic mice.
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- Spiny keratoderma ‐ a demonstration of hair keratin and hair type keratinization