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- Hair follicle differentiation: expression, structure and evolutionary conservation of the hair type II keratin intermediate filament gene family
- 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
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes
- Complete sequence of a hair-like intermediate filament type II keratin gene
- Unique amino acid signatures that are evolutionarily conserved distinguish simple-type, epidermal and hair keratins
- The human type I keratin gene family: Characterization of new hair follicle specific members and evaluation of the chromosome 17q21.2 gene domain
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- <i>In vitro</i> Assembly Properties of Human Type I and II Hair Keratins
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- Type II Epithelial Keratin 6hf (K6hf) Is Expressed in the Companion Layer, Matrix, and Medulla in Anagen-Stage Hair Follicles
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Sequences and differential expression of three novel human type-II hair keratins
- 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 Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- A novel human type I hair keratin gene: evidence for two keratin hHa3 isoforms
- 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
- 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 hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Expression of type I hair keratins in follicular tumours
- A cDNA encoding the human type I hair keratin hHa1
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Sequence and Expression of Murine Type I Hair Keratins mHa2 and mHa3
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle