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Research 30 of 1000+
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Characterization of a 190-Kilobase Pair Domain of Human Type I Hair Keratin Genes
- Novel Type I Hair Keratins K39 and K40 Are the Last to be Expressed in Differentiation of the Hair: Completion of the Human Hair Keratin Catalog
- Sequences and differential expression of three novel human type-II hair keratins
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Sequence and Expression of Murine Type I Hair Keratins mHa2 and mHa3
- 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
- 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
- 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
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Hair follicle differentiation: expression, structure and evolutionary conservation of the hair type II keratin intermediate filament gene family
- Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Sequence analyses of Type I and Type II chains in human hair and epithelial keratin intermediate filaments: Promiscuous obligate heterodimers, Type II template for molecule formation and a rationale for heterodimer formation
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- Unique amino acid signatures that are evolutionarily conserved distinguish simple-type, epidermal and hair keratins
- <i>In vitro</i> Assembly Properties of Human Type I and II Hair Keratins