Published in Hum Mutat on March 01, 2008
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Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12. Eye (Lond) (2012) 0.78
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Human keratin 8 variants promote mouse acetaminophen hepatotoxicity coupled with c-jun amino-terminal kinase activation and protein adduct formation. Hepatology (2015) 0.76
Avascular necrosis of the hip and diffuse idiopathic skeletal hyperostosis during long-term isotretinoin treatment of epidermolytic ichthyosis due to a novel deletion mutation in KRT10. Br J Dermatol (2014) 0.75
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Müller glia reactivity follows retinal injury despite the absence of the glial fibrillary acidic protein gene in Xenopus. Dev Biol (2016) 0.75
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Novel sporadic and recurrent mutations in KRT5 and KRT14 genes in Polish epidermolysis bullosa simplex patients: further insights into epidemiology and genotype-phenotype correlation. J Appl Genet (2015) 0.75
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Deacetylase inhibition promotes the generation and function of regulatory T cells. Nat Med (2007) 6.61
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New consensus nomenclature for mammalian keratins. J Cell Biol (2006) 3.27
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