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KRT14 gene

Known as: KRT14, Keratin 14 Gene, KERATIN 14, TYPE I 
This gene is involved in the regulation of cell shape.
National Institutes of Health

Related topics

Related topics

9 relations
Cell MovementCytokinesisCytoskeletal ModelingKRT1 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Digenic inheritance of KRT5 and KRT14 mutations in a family with epidermolysis bullosa simplex
2011; 241: 180–205. 4. Podojil JR, Miller SD. Potential targeting of B7–H4 for the treatment of cancer. Immunol. Rev. 2017; 276… 
2020
2020
A nonsense variant in the KRT14 gene in a domestic shorthair cat with epidermolysis bullosa simplex.
Epidermolysis bullosa simplex (EBS) is a hereditary blistering disease affecting the skin and mucous membranes. It has been… 
2016
2016
Genotypic Heterogeneity and the Mode of Inheritance in Epidermolysis Bullosa.
Epidermolysis bullosa (EB) comprises a clinically heterogeneousgroupofdisorderscharacterizedbyfragilityof skin, leading to… 
2014
2014
SYNTHESIS, CHARACTERIZATION AND STUDY OF SOME N -SUBSTITUTED ARYL-2- ({4- [(SUBSTITUTED ARYL CARBAMOYL) METHYL] -5- (PYRIDIN-4-YL) -4 H -1, 2, 4-TRIAZOL-3-YL} SULFANYL) ACETAMIDE
Pathogenic infections and inflammation are very common ailments humans suffer. Upsurge of resistant pathogens has impeded the… 
2009
2009
A novel mutation (p.Thr198Ser) in the 1A helix of keratin 5 causes the localized variant of Epidermolysis Bullosa Simplex
Abstract:  A novel missense mutation (p.Thr198Ser) in the 1A helix of keratin 5 (K5) has been identified in a four‐generation… 
Review
2003
Review
2003
Mutation analysis of the entire keratin 5 and 14 genes in patients with epidermolysis bullosa simplex and identification of novel mutations
Epidermolysis bullosa simplex is a group of blistering skin disorders caused by defects in one of the keratin genes, KRT5 and… 
2003
2003
Functional testing of keratin 14 mutant proteins associated with the three major subtypes of epidermolysis bullosa simplex
Abstract: Epidermolysis bullosa simplex (EBS) is a group of autosomal dominantly inherited skin disorders characterized by the… 
2002
2002
A Novel Nonsense Mutation at E106 of the 2B Rod Domain of Keratin 14 Causes Dominant Epidermolysis Bullosa Simplex
Epidermolysis bullosa simplex (EBS) is classified into three main types and is caused, in most cases, by missense mutations in… 
1978
1978
Cockade-like vitiligo and linear vitiligo
SummaryThe authors report 2 cases of atypical vitiligo in which they observed 1) “cockade-like” lesions resembling those of… 
1977
1977
Disturbance of DNA-synthesis in early psoriasis
SummaryIn earlier studies we have shown that there is a significant prolongation of DNA-synthesis time (ts) in the epidermal… 
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