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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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2012
2012
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
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
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
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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1995
1995
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
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 keratosis (EPPK) cosegregates with breast and ovarian cancers in a large French pedigree, raising the… Expand
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1994
1994
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
SummaryEpidermolytic palmoplantar keratoderma (EPPK) (Vörner-Unna-Thost) is an autosomal dominantly inherited skin disease of… Expand
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