|1.||Hausser, I: 3 articles (01/2012 - 02/2009)|
|2.||Arin, M J: 3 articles (02/2011 - 02/2000)|
|3.||McLean, W H Irwin: 3 articles (03/2006 - 05/2002)|
|4.||Richard, Gabriele: 3 articles (01/2006 - 03/2003)|
|5.||Shimizu, Hiroshi: 2 articles (05/2011 - 06/2007)|
|6.||Sakai, Kaori: 2 articles (05/2011 - 06/2007)|
|7.||Akiyama, Masashi: 2 articles (05/2011 - 06/2007)|
|8.||Oji, V: 2 articles (02/2011 - 02/2009)|
|9.||Grimberg, G: 2 articles (02/2011 - 02/2009)|
|10.||Krieg, T: 2 articles (02/2011 - 02/2009)|
|1.||Epidermolytic Hyperkeratosis (Bullous Congenital Ichthyosiform Erythroderma)
02/01/2012 - "A recurrent missense mutation of keratin 1 gene in a Chinese family with epidermolytic hyperkeratosis (severe palmoplantar hyperkeratosis, type 1)."
05/01/2011 - "Extremely severe palmoplantar hyperkeratosis in a generalized epidermolytic hyperkeratosis patient with a keratin 1 gene mutation."
09/01/2006 - "Identification of a de novo keratin 1 mutation in epidermolytic hyperkeratosis with palmoplantar involvement."
08/01/2006 - "A novel mutation of the keratin 1 gene in a family with epidermolytic hyperkeratosis."
05/01/2006 - "A mouse keratin 1 mutation causes dark skin and epidermolytic hyperkeratosis."
10/10/2005 - "These communities of tumor cells underwent autonomous growth that was associated with altered expression of markers of differentiation (keratin 1) and cell-cell communication (connexin-43). "
08/01/2001 - "Keratin 1 expression in endothelia and mesenchymal tumors: an immunohistochemical analysis of normal and neoplastic tissues."
07/09/1998 - "To develop an in vivo model for studying the role of the p53 tumor suppressor in skin carcinogenesis, a murine p53(172H) mutant (equivalent to human p53(175H)) was expressed in the epidermis of transgenic mice, utilizing a targeting vector based on the human keratin 1 gene (HK1.p53m). "
03/01/2008 - "Treatment of primary mouse keratinocytes with Cripto-1 stimulated proliferation and induced expression of keratin 8 but blocked induction of the normal epidermal differentiation marker keratin 1, changes that are hallmarks of tumor progression in squamous cancer. "
05/01/2002 - "Keratin expression in human tissues and neoplasms Keratin filaments constitute type I and type II intermediate filaments (IFs), with at least 20 subtypes named keratin 1-20. "
03/01/2003 - "In vivo studies of mutant keratin 1 in ichthyosis hystrix Curth-Macklin."
01/01/2013 - "Epidermolytic ichthyosis (EI) is an autosomal dominant epidermal skin fragility disorder caused by mutations in keratin 1 and 10 (K1 and K10) genes. "
01/01/2012 - "This congenital Ichthyosis occurs due to mutations of keratin 1 or 10 genes that leads to defects of intra- and intercellular structural integrity in the spinous and granular layers with compensatory hyperkeratosis. "
04/01/2010 - "A novel mutation in the L12 domain of keratin 1 is associated with mild epidermolytic ichthyosis."
10/01/2002 - "Here we present two novel mutations in the keratin 1 gene (KRT1): a 5' donor splice site mutation in exon 1 (591 + 2T > A) that predicts a 22 amino acid in-frame deletion in the keratin 1 1A domain; and an in-frame deletion in exon 7 (1376del24) that predicts a foreshortened 2B coiled-coil domain of keratin 1. In each case these mutations are associated with palmoplantar keratoderma and mild ichthyosis, largely limited to the flexural areas. "
|4.||Epidermolysis Bullosa Simplex (Epidermolysis Bullosa Herpetiformis Dowling Meara)
04/01/2003 - "In this study, we report two novel frameshift mutations that are predicted to alter the tail of keratin 1 or keratin 5, leading to an atypical form of epidermolytic hyperkeratosis and a mild form of epidermolysis bullosa simplex, respectively. "
04/01/2003 - "Epidermolytic hyperkeratosis and epidermolysis bullosa simplex caused by frameshift mutations altering the v2 tail domains of keratin 1 and keratin 5."
01/01/2006 - "Instead, they have been associated with several distinct clinical phenotypes, such as epidermolysis bullosa simplex with mottled pigmentation (mutation P25L in the V1 domain of keratin 5), epidermolysis bullosa simplex with migratory circinate erythema (frameshift mutation c1649delG in the V2 domain of keratin 5), striate palmoplantar keratoderma (PPK), and ichthyosis hystrix Curth-Macklin (different frameshift mutations in the V2 domain of keratin 1 (K1)). "
11/01/2013 - "Studies of the polymorphisms of the Keratin 1 (KRT1) gene have been driven mostly by interest in its role in skin diseases. "
09/01/2006 - "Epidermolytic hyperkeratosis (EHK) (OMIM 113800) is a generalized skin disease with mostly autosomal dominant inheritance, caused by mutations in keratin 1 or keratin 10. "
|3.||Keratin-5 (Keratin 5)
|4.||Keratin-13 (Keratin 13)
|10.||Keratin-2 (Keratin 2)