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- 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
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11
- The human type I keratin gene family: Characterization of new hair follicle specific members and evaluation of the chromosome 17q21.2 gene domain
- A novel point mutation of keratin 17 (<i>KRT17</i>) in a Japanese family with pachyonychia congenita type 2: an RNA-based genetic analysis using a single hair bulb
- Type 2 Diabetic Mellitus Inhibits Skin Renewal through Inhibiting WNT-Dependent Lgr5+ Hair Follicle Stem Cell Activation in C57BL/6 Mice
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Peer Review #1 of "Potential use of human hair shaft keratin peptide signatures to distinguish gender and ethnicity (v0.2)"
- Evolution of Trichocyte Keratins
- Advances in molecular pathogenesis of hidradenitis suppurativa: Dysregulated keratins and ECM signaling
- <i>In vivo</i> alteration of the keratin 17 gene in hair follicles by oligonucleotide‐directed gene targeting
- Keratin Gene Expression Differences in Wool Follicles and Sequence Diversity of High Glycine-Tyrosine Keratin-Associated Proteins (Kaps) in Magra Sheep of India
- <i>In vitro</i> Assembly Properties of Human Type I and II Hair Keratins
- The Type I Keratin 19 Possesses Distinct and Context-dependent Assembly Properties
- Interventional and Intrinsic Airway Homeostasis and Repair
- The Human Type II Keratin Gene Cluster on Chromosome 12q13.13: Final Count or Hidden Secrets?
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Decision letter: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Identification of key genes and signaling pathways related to Hetian sheep wool density by RNA-seq technology
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- A novel human type I hair keratin gene: evidence for two keratin hHa3 isoforms
- Differential expression of type I IRS keratin genes in three breeds of sheep
- Crosslinking structure of keratin. V. Number and type of crosslinks in microstructures of untreated and potassium cyanide treated human hair
- Crosslinking structure of keratin. V. Number and type of crosslinks in microstructures of untreated and potassium cyanide treated human hair
- Unique amino acid signatures that are evolutionarily conserved distinguish simple-type, epidermal and hair keratins
- Structure and Mechanical Properties of Human Trichocyte Keratin Intermediate Filament Protein