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KRT9 gene

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

Papers overview

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2006
2006
Epidermolytic palmoplantar keratoderma (EPPK) is an autosomal dominant genodermatosis characterized by epidermolytic… Expand
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2004
2004
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
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
BACKGROUND Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disease of unknown etiology that causes… Expand
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1997
1997
Keratin 9 mutation was examined in a Japanese kindred of epidermolytic palmoplantar keratoderma (EPPK), which is a dominantly… Expand
1996
1996
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
Epidermolytic palmoplantar keratoderma is an autosomal dominant skin disorder characterized by hyperkeratosis of the palms and… Expand
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1995
1995
Palmoplantar keratoderma of Voerner type (or epidermolytic palmoplantar keratoderma) is an autosomal dominant inherited disorder… Expand
Highly Cited
1994
Highly Cited
1994
We have isolated the gene for human type I keratin 9 (KRT9) and localised it to chromosome 17q21. Patients with epidermolytic… Expand
1994
1994
Hereditary palmoplantar keratoderma is characterized by hyperkeratosis of the skin of palms and soles. An autosomal dominant form… Expand