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Research 331–360 of 1000+
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- KERATINS AND SKIN DISORDERS
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- Faculty Opinions recommendation of Identification of novel hair-growth inducers by means of connectivity mapping.
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- Chromosomal localization of acidic and basic keratin genes of the domestic dog
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- Expression pattern of human hair keratin basic 1 (hHbl) in hair follicle and pilomatricoma
- 474 Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Effects of Food-Derived Collagen Peptides on the Expression of Keratin and Keratin-Associated Protein Genes in the Mouse Skin
- Revisiting the significance of keratin expression in complex epithelia
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- Ichthyosis follicularis with alopecia and photophobia syndrome with coexisting palmoplantar keratoderma treated with acitretin
- Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay
- 440 Topical application of anti-cancer drug Bortezomib stimulates proliferation of follicular cells and induces expression of hair keratins via GATA-3 transcription factor
- Loss of keratin 10 is accompanied by increased sebocyte proliferation and differentiation
- Genes for Hair and Avian Keratins
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation
- Keratins: the hair shaft's backbone revealed
- Characterization of Bsk mice: I. The Bsk mutation does not involve a recombination of cornea-specific keratin 12 and skin-specific hair keratin genes.
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- The keratin 19 promoter is potent for cell-specific targeting of genes in transgenic mice
- Discovery of a novel murine keratin 6 (K6) isoform explains the absence of hair and nail defects in mice deficient for K6a and K6b
- Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humans