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FERMT1 gene

Known as: C20ORF42, kindlin-1, CHROMOSOME 20 OPEN READING FRAME 42 
National Institutes of Health

Papers overview

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2017
2017
Kindlin-2 (K2), a 4.1R-ezrin-radixin-moesin (FERM) domain adaptor protein, mediates numerous cellular responses, including… 
2014
2014
Kindler syndrome (KS) in humans is a severe skin blistering disease associated with inflammation and increased risk of epidermal… 
2013
2013
Kindlin-1 binds to integrins and regulates integrin activation at cell adhesions. Here we report a new function of Kindlin-1 in… 
2012
2012
Kindlin-1 is an adaptor protein that is expressed by most epithelial cells and has been implicated in integrin bidirectional… 
Review
2009
Review
2009
ZusammenfassungDas Kindler-Syndrom ist eine neue Form der Epidermolysis bullosa hereditaria und die erste Genodermatose, die… 
Review
2004
Review
2004
Kindler syndrome is a rare, autosomal recessive skin fragility disorder characterized by blistering in infancy, followed by… 
1994
1994
The nucleotide sequence of a 12·5 kb fragment localized to the right arm of chromosome II of Saccharomyces cerevisiae has been…