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KRT6A gene

Known as: CK6C, K6A, CK6D 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Introduction Pachyonychia Congenital is a rare, but well-characterized autosomal dominant disorder of keratinization… 
Review
2016
Review
2016
Pachyonychia congenita (PC) is a rare autosomal dominant genodermatosis with an estimated incidence of only 5,000 to 10,000… 
2006
2006
CaN19, a member of the S100 family of calcium-binding proteins, Is known to be “underexpressed― in cultured breast carcinoma… 
2003
2003
Pachyonychia congenita (PC) is a rare genodermatosis affecting the nails and other ectodermal tissues. It is mainly characterized… 
2001
2001
![Graphic][1] ARNO (green) activates cell movement. Stationary cells sometimes undergo a dramatic morphological change and… 
2001
2001
![Graphic][1] Platelets (green) produce IL-1β (red) during a clotting reaction. Platelets get no respect. Traditionally, these… 
1972
1972
To determine the molecular basis of transformation defects in Haemophilus influenzae, the fate of genetically marked, 32P-labeled… 
1967
1967
Cell-free extracts of Streptococcus faecalis N83 and Streptococcus faecium K6A were shown to possess comparable enzyme systems… 
1966
1966
Tucker, Fayne L. (University of Southern California, Los Angeles), John W. Thomas, Milo D. Appleman, Stewart H. Goodman, and…