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KRT1 gene

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

Related topics

Related topics

15 relations
Cell MovementCytokeratinCytokeratin test systemCytokinesis

Narrower (1)

KRT1 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2015
Highly Cited
2015
Frequent somatic reversion of KRT1 mutations in ichthyosis with confetti.
Widespread reversion of genetic disease is rare; however, such events are particularly evident in some skin disorders in which… 
Highly Cited
2002
Highly Cited
2002
Factor XII interacts with the multiprotein assembly of urokinase plasminogen activator receptor, gC1qR, and cytokeratin 1 on endothelial cell membranes.
Investigations were performed to define the factor XII (FXII) binding site(s) on cultured endothelial cells (HUVECs). Biotin- or… 
Review
2002
Review
2002
The plasma kallikrein-kinin system counterbalances the renin-angiotensin system.
  • A. Schmaier
  • 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… 
Review
2002
Review
2002
Assembly and activation of the plasma kallikrein/kinin system: a new interpretation.
Highly Cited
2002
Highly Cited
2002
Frameshift mutation in the V2 domain of human keratin 1 results in striate palmoplantar keratoderma.
The striate form of palmoplantar keratoderma is a rare autosomal dominant disorder affecting palm and sole skin. Genetic… 
Highly Cited
2001
Highly Cited
2001
Expression and colocalization of cytokeratin 1 and urokinase plasminogen activator receptor on endothelial cells.
The cellular localization of human cytokeratin 1 (CK1), urokinase plasminogen activator receptor (uPAR), and gC1qR, high… 
Highly Cited
2001
Highly Cited
2001
Endothelial oxidative stress activates the lectin complement pathway: role of cytokeratin 1.
Highly Cited
1994
Highly Cited
1994
Mutations in the H1 and 1A domains in the keratin 1 gene in epidermolytic hyperkeratosis.
In the autosomal dominant disorder epidermolytic hyperkeratosis, the structural integrity of the keratin intermediate filaments… 
Highly Cited
1993
Highly Cited
1993
Identification of control elements 3' to the human keratin 1 gene that regulate cell type and differentiation-specific expression.
Highly Cited
1992
Highly Cited
1992
A leucine→proline mutation in the H1 subdomain of keratin 1 causes epidermolytic hyperkeratosis
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