KRT10 gene

Known as: cytokeratin 10, epidermolytic hyperkeratosis, KERATIN 10, TYPE I 
This gene plays a role in intermediate filament structure.
National Institutes of Health

Topic mentions per year

Topic mentions per year

1961-2018
05101519612018

Papers overview

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2010
2010
Somatic loss of wild-type alleles can produce disease traits such as neoplasia. Conversely, somatic loss of disease-causing… (More)
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Highly Cited
2008
Highly Cited
2008
BACKGROUND Staphylococcus aureus permanently colonizes the vestibulum nasi of one-fifth of the human population, which is a risk… (More)
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2008
2008
A number of clubroot resistant (CR) Chinese cabbage cultivars have been developed in Japan using resistant genes from CR European… (More)
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2007
2007
OBJECTIVE The K10 and K6 are short rating scales designed to detect individuals at risk for depressive disorder, with or without… (More)
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2004
2004
The primary habitat of Staphylococcus aureus in humans is the moist squamous epithelium of the anterior nares. We showed… (More)
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1999
1999
The epidermis forms a vital barrier composed of stratified keratinocytes and their differentiated products. One of these products… (More)
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1996
1996
Lesional psoriatic epidermis displays a number of phenotypic changes that are distinct from the differentiation program found in… (More)
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Highly Cited
1995
Highly Cited
1995
The human endogenous retrovirus K10 (HERV-K10) has been identified in the human genome by its homology to retroviruses of other… (More)
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1995
1995
The establishment of dorsoventral polarity in the Drosophila oocyte and future embryo is dependent on the efficient transport of… (More)
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1992
1992
Epidermolytic hyperkeratosis (EH; previously called bullous congenital ichthyosiform erythroderma) is an autosomal dominant skin… (More)
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