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Research 30 of 1000+
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Hair follicle differentiation: expression, structure and evolutionary conservation of the hair type II keratin intermediate filament gene family
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Characterization of New Members of the Human Type II Keratin Gene Family and a General Evaluation of the Keratin Gene Domain on Chromosome 12q13.13
- Detection of Type IIHair Keratin Gene in a Family with Monilethrix
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Mutation analysis of the typeIIhair keratin gene in a family of Han nationality with monilethrix
- Keratin Gene Expression in Wool Fibre Development
- Genome-wide identification, characterization, and expression analysis of keratin genes (KRTs) family in yak (Bos grunniens)
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- Multiomics Analysis of the Response to Ritlecitinib in Alopecia Areata Subtypes and Correlation With Efficacy
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Evolution of Trichocyte Keratins
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- Convergent evolution has led to the loss of claw proteins in snakes and worm lizards
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- A family of type I keratin genes and the homeobox-2 gene complex are closely linked to the rex locus on mouse chromosome 11
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Chromosomal localization of acidic and basic keratin genes of the domestic dog
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Increased rate of hair keratin gene loss in the cetacean lineage
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Genes for intermediate filament proteins and the draft sequence of the human genome