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KRT6C gene

Known as: KERATIN 6H, KERATIN 6C, TYPE II, K6C 
National Institutes of Health

Related topics

Related topics

3 relations
KRT6A geneKRT72 geneKRT8 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
The histopathological features of the nail plate in pachyonychia congenita
Pachyonychia congenita (PC) is a rare autosomal dominant disorder of keratinization mediated by genetic mutations in KRT6A, KRT6B… 
Review
2019
Review
2019
A KRT16 mutation in the first Chinese pedigree with Pachyonychia congenita and review of the literatures
Pachyonychia congenita (PC), a rare autosomal dominant disorder, is featured by significant hypertrophic nail, palmoplantar… 
2018
2018
Novel weak form quadrature elements for non-classical higher order beam and plate theories
Based on Lagrange and Hermite interpolation two novel versions of weak form quadrature element are proposed for a non-classical… 
2017
2017
NANOCOMPOSITE, ITS TOXICITY REDUCTION, AND SUSTAINED RELEASE
Objectives: Polyoxometalates (POMs) are proved to be important for applications in medicine and in material science. Here, we… 
2016
2016
Focal PPK secondary to a novel KRT6C mutation (Pachyonychia congenita‐K6c)
1 Willemze R, Jaffe ES, Burg G et al. WHO-EORTC classification for cutaneous lymphomas. Blood 2005; 105 3768–3785. 2 Sugaya M… 
2013
2013
Collapse of the keratin filament network through the expression of mutant keratin 6c observed in a case of focal plantar keratoderma
Focal palmoplantar keratoderma (PPK) with severe pain is a hallmark of pachyonychia congenita, a rare autosomal dominant disorder… 
2011
2011
Diffuse and focal palmoplantar keratoderma can be caused by a keratin 6c mutation
The palmoplantar keratodermas (PPKs) are a large group of genodermatoses comprising nearly 60 genetically distinct diseases. They… 
2009
2009
The dipole moment of the electron carrier adrenodoxin is not critical for redox partner interaction and electron transfer.
Highly Cited
1997
Highly Cited
1997
Phosphorylation of Human Keratin 8 in Vivo at Conserved Head Domain Serine 23 and at Epidermal Growth Factor-stimulated Tail Domain Serine 431*
Dynamic phosphorylation is one mechanism that regulates the more than 20 keratin type I and II intermediate filament proteins in… 
1993
1993
Analysis of a genetic mutation in an electrophoretic variant of the human lactate dehydrogenase-B(H) subunit
An electrophoretic variant of the lactate dehydrogenase (LDH)-B(H) subunit was discovered in a patient with diabetes mellitus… 
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