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KRT9 gene

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

Related topics

Related topics

5 relations
KRT1 wt AlleleKRT8 geneKeratin-9Keratoderma, Palmoplantar, Diffuse
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Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2006
2006
Mutation S233L in the 1B domain of keratin 1 causes epidermolytic palmoplantar keratoderma with "tonotubular" keratin.
Epidermolytic palmoplantar keratoderma (EPPK) is an autosomal dominant genodermatosis characterized by epidermolytic… Expand
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2004
2004
Keratin 9 gene mutational heterogeneity in patients with epidermolytic palmoplantar keratoderma
Mutations in the human keratin 9 gene have recently been shown to be involved in the etiology of palmoplantar keratoderma (PPK… Expand
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Highly Cited
2001
Highly Cited
2001
Mesoscale Modeling of Katabatic Winds over Greenland with the Polar MM5
Abstract Verification of two months, April and May 1997, of 48-h mesoscale model simulations of the atmospheric state around… Expand
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Highly Cited
1998
Highly Cited
1998
Gene for arrhythmogenic right ventricular cardiomyopathy with diffuse nonepidermolytic palmoplantar keratoderma and woolly hair (Naxos disease) maps to 17q21.
BACKGROUND Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disease of unknown etiology that causes… Expand
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1997
1997
A novel mutation of a leucine residue in coil 1A of keratin 9 in epidermolytic palmoplantar keratoderma.
Keratin 9 mutation was examined in a Japanese kindred of epidermolytic palmoplantar keratoderma (EPPK), which is a dominantly… Expand
1996
1996
Keratin 9 point mutation in the pedigree of epidermolytic hereditary palmoplantar keratoderma perturbs keratin intermediate filament network formation
Keratins form an intracellular keratin filament network in keratinocytes. Point mutations in the epidermal keratins could lead to… Expand
Highly Cited
1995
Highly Cited
1995
Mutations in the 1A domain of keratin 9 in patients with epidermolytic palmoplantar keratoderma.
Epidermolytic palmoplantar keratoderma is an autosomal dominant skin disorder characterized by hyperkeratosis of the palms and… Expand
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1995
1995
Ultrastructural changes resulting from keratin-9 gene mutations in two families with epidermolytic palmoplantar keratoderma.
Palmoplantar keratoderma of Voerner type (or epidermolytic palmoplantar keratoderma) is an autosomal dominant inherited disorder… Expand
Highly Cited
1994
Highly Cited
1994
Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK)
We have isolated the gene for human type I keratin 9 (KRT9) and localised it to chromosome 17q21. Patients with epidermolytic… Expand
1994
1994
The gene for diffuse palmoplantar keratoderma of the type found in northern Sweden is localized to chromosome 12q11-q13.
Hereditary palmoplantar keratoderma is characterized by hyperkeratosis of the skin of palms and soles. An autosomal dominant form… Expand
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