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KRT1 gene

Known as: keratin 1, KRT1, K1 
This gene is involved in skin development.
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2004
Highly Cited
2004
ABSTRACT In resting cells, the NFAT1 transcription factor is kept inactive in the cytoplasm by phosphorylation on multiple serine… Expand
Review
2002
Review
2002
Understanding the importance and physiologic activity of the plasma kallikrein/kinin system (KKS) has been thwarted by the… Expand
Highly Cited
2002
Highly Cited
2002
Investigations were performed to define the factor XII (FXII) binding site(s) on cultured endothelial cells (HUVECs). Biotin- or… Expand
Highly Cited
2002
Highly Cited
2002
The striate form of palmoplantar keratoderma is a rare autosomal dominant disorder affecting palm and sole skin. Genetic… Expand
Review
2002
Review
2002
  • A. Schmaier
  • The Journal of clinical investigation
  • 2002
  • Corpus ID: 15045466
The plasma kallikrein-kinin system (KKS), first recognized over 40 years ago, was originally believed to contribute to… Expand
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Highly Cited
2001
Highly Cited
2001
Oxidative stress increases endothelial mannose-binding lectin (MBL) binding and activates the lectin complement pathway (LCP… Expand
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Highly Cited
2001
Highly Cited
2001
The cellular localization of human cytokeratin 1 (CK1), urokinase plasminogen activator receptor (uPAR), and gC1qR, high… Expand
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Highly Cited
1994
Highly Cited
1994
In the autosomal dominant disorder epidermolytic hyperkeratosis, the structural integrity of the keratin intermediate filaments… Expand
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Highly Cited
1993
Highly Cited
1993
To define DNA regulatory elements that mediate the response of the keratin 1 (K1) gene to Ca(2+)-induced differentiation, regions… Expand
Highly Cited
1992
Highly Cited
1992
Epidermolytic hyperkeratosis is an autosomal dominant disorder affecting the structural integrity of the suprabasal layers of… Expand