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KRT9 gene

Known as: KERATIN 9, TYPE I, type I cytoskeletal 9, KA9 
National Institutes of Health

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KRT1 wt AlleleKRT8 geneKeratin-9Keratoderma, Palmoplantar, Diffuse

Papers overview

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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… 
2011
2011
A novel mutation within the 2B rod domain of keratin 9 in a Chinese pedigree with epidermolytic palmoplantar keratoderma combined with knuckle pads and camptodactyly.
Knuckle pads and camptodactyly are overlapping symptoms associated with many genetic and environmental factors. To the best of… 
2010
2010
A novel mutation of the keratin 9 gene in a Chinese family with epidermolytic palmoplantar keratoderma
women aged <55 years is associated with coronary artery disease according to angiographic studies, but did not study lipid levels… 
2009
2009
Knuckle pads, in an epidermal palmoplantar keratoderma patient with Keratin 9 R163W transgrediens expression.
Epidermolytic PalmoPlantar keratoderma (EPPK) Vörner-type is an autosomal dominantly inherited skin disease, characterized by… 
2009
2009
Prenatal diagnosis of epidermolytic palmoplantar keratoderma caused by c.T470C (p.M157T) of the keratin 9 gene in a Chinese kindred
X.-L. Chen1†, C.-M. Xu2†, S.-R. Cai3†, C.-Y. Chen1 and X.-N. Zhang1* 1Institute of Cell Biology and Department of Biochemistry… 
2003
2003
A novel mutation of keratin 9 in epidermolytic palmoplantar keratoderma combined with knuckle pads
Epidermolytic palmoplantar keratoderma (EPPK) is an autosomal dominantly inherited disease. We studied a family from Shandong… 
1999
1999
Keratin 9 Mutations in the Coil 1A Region in Epidermolytic Palmoplantar Keratoderma
Abstract: The palmoplantar keratodermas (PPK) are a heterogeneous group of conditions, most frequently inherited in autosomal… 
1999
1999
A case of spontaneous mutation in the keratin 9 gene associated with epidermolytic palmoplantar keratoderma
Epidermolytic palmoplantar keratoderma appears to be due to defects in keratin 9, the palmoplantar specific type 1 keratin. We… 
1998
1998
Mutations in the 1A rod domain segment of the keratin 9 gene in epidermolytic palmoplantar keratoderma.
Palmoplantar keratodermas (PPK) constitute a heterogeneous group of diseases marked by the thickening of palms and soles of… 
1992
1992
Mapping of a gene for epidermolytic palmoplantar keratoderma to the region of the acidic keratin gene cluster at 17q12–q21
SummaryEpidermolytic palmoplantar keratoderma (EPPK) (Vörner-Unna-Thost) is an autosomal dominantly inherited skin disease of… 
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