KRT9 gene

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

Topic mentions per year

Topic mentions per year

1959-2017
051019592017

Papers overview

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2014
2014
Methylation of histone H3 on lysine 9 or 27 is crucial for heterochromatin formation. Previously considered hallmarks of… (More)
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2009
2009
The enzymological properties of AtAurora1, a kinase responsible for the cell cycle-dependent phosphorylation of histone H3 at S10… (More)
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2009
2009
Class switch recombination (CSR) involves a DNA rearrangement in the Ig heavy chain (IgH) gene that allows the same variable (V… (More)
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Highly Cited
2006
Highly Cited
2006
In Arabidopsis thaliana, heterochromatin formation is guided by double-stranded RNA (dsRNA), which triggers methylation of… (More)
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2006
2006
Tylosis (focal non-epidermolytic palmoplantar keratoderma) is an autosomal dominant skin disorder that is associated with the… (More)
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2005
2005
Histones are modified post-translationally, e.g. by methylation of lysine and arginine residues, and by phosphorylation of serine… (More)
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2003
2003
Facultative heterochromatin is a cytological manifestation of epigenetic mechanisms that regulate gene expression. Constitutive… (More)
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1999
1999
Palms and soles differ from other body sites in terms of clinical and histologic appearance, response to mechanical stress, and… (More)
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1995
1995
Keratins K6 and K16 are expressed in suprabasal interfollicular epidermis in wound healing and other pathological conditions… (More)
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1994
1994
We have isolated the gene for human type I keratin 9 (KRT9) and localised it to chromosome 17q21. Patients with epidermolytic… (More)
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