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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

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2012
2012
Proteomic analysis of the cerebrospinal fluid in multiple sclerosis and neuromyelitis optica patients.
The present study aimed to compare the 2-dimensional (2D) electrophoresis pattern of the cerebrospinal fluid (CSF) in multiple… Expand
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2005
2005
One-loop weak corrections to hadronic production of Z bosons at large transverse momenta
To match the precision of present and future measurements of Z-boson production at hadron colliders, electroweak radiative… Expand
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2005
2005
Mating-type Distribution and Fertility Status in Magnaporthe grisea Populations from Argentina
Isolates of Magnaporthe grisea causing gray leaf spot on rice were collected in Argentina and analyzed for mating distribution… 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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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
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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
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1994
1994
Epidermolytic palmoplantar keratoderma cosegregates with a keratin 9 mutation in a pedigree with breast and ovarian cancer
Epidermolytic palmoplantar keratosis (EPPK) cosegregates with breast and ovarian cancers in a large French pedigree, raising the… Expand
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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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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… Expand
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