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Research 30 of 1000+
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- 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
- 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
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- A novel human type I hair keratin gene: evidence for two keratin hHa3 isoforms
- 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
- 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
- The human type I keratin gene family: Characterization of new hair follicle specific members and evaluation of the chromosome 17q21.2 gene domain
- Complete sequence of a hair-like intermediate filament type II keratin gene
- Hair follicle differentiation: expression, structure and evolutionary conservation of the hair type II keratin intermediate filament gene family
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Hair-Specific Keratins: Characterization and Expression of a Mouse Type I Keratin Gene
- A Unique Type I Keratin Intermediate Filament Gene Family is Abundantly Expressed in the Inner Root Sheaths of Sheep and Human Hair Follicles
- Genomic Characterization of the Human Type I Cuticular Hair Keratin hHa2 and Identification of an Adjacent Novel Type I Hair Keratin Gene hHa5
- The Region Coding for the Helix Termination Motif and the Adjacent Intron 6 of the Human Type I Hair Keratin Gene hHa2 Contains Three Natural, Closely Spaced Polymorphic Sites
- Characterization of a Cluster of Human High/Ultrahigh Sulfur Keratin-associated Protein Genes Embedded in the Type I Keratin Gene Domain on Chromosome 17q12-21
- Detection of Type IIHair Keratin Gene in a Family with Monilethrix
- 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
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Sequence and expression of human hair keratin genes
- Characterization and Chromosomal Localization of Human Hair-Specific Keratin Genes and Comparative Expression During the Hair Growth Cycle
- Differential expression of type I IRS keratin genes in three breeds of sheep
- Increased rate of hair keratin gene loss in the cetacean lineage
- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11