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Research 61–90 of 1000+
- Complete sequence of a hair-like intermediate filament type II keratin gene
- 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
- Sequence of a Cashmere goat type I hair keratin gene and its expression in skin
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- Sequences and differential expression of three novel human type-II hair keratins
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Sequence Data and Chromosomal Localization of Human Type I and Type II Hair Keratin Genes
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- Hair follicle differentiation: expression, structure and evolutionary conservation of the hair type II keratin intermediate filament gene family
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- Expression analysis of the type I keratin protein keratin 33A in goat coat hair
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- 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
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- A Unique Type I Keratin Intermediate Filament Gene Family is Abundantly Expressed in the Inner Root Sheaths of Sheep and Human Hair Follicles
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Structure and site of expression of a murine type II hair keratin
- Detection of Type IIHair Keratin Gene in a Family with Monilethrix
- Cachexia and graft-vs.-host-disease-type skin changes in keratin promoter-driven TNF alpha transgenic mice.
- Sequence and Expression of Murine Type I Hair Keratins mHa2 and mHa3
- Expression of type I hair keratins in follicular tumours
- A cDNA encoding the human type I hair keratin hHa1