FAQ

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

Related topics

Related topics

5 relations
KRT1 wt AlleleKRT8 geneKeratin-9Keratoderma, Palmoplantar, Diffuse
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Related mentions per year

Related mentions per year

1949-2018
19401960198020002020
KRT9 gene
KRT8 gene
Keratoderma, Palmoplantar, Diffuse
Keratoderma, Palmoplantar, Epidermolytic
KRT1 wt Allele
Keratin-9

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Polycomb repressive complex 2 and H3K27me3 cooperate with H3K9 methylation to maintain heterochromatin protein 1α at chromatin.
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
Aurora1 phosphorylation activity on histone H3 and its cross-talk with other post-translational histone modifications in Arabidopsis.
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
H3 trimethyl K9 and H3 acetyl K9 chromatin modifications are associated with class switch recombination.
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
Locus-specific control of DNA methylation by the Arabidopsis SUVH5 histone methyltransferase.
In Arabidopsis thaliana, heterochromatin formation is guided by double-stranded RNA (dsRNA), which triggers methylation of… (More)
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2006
2006
Down-regulation of the cytoglobin gene, located on 17q25, in tylosis with oesophageal cancer (TOC): evidence for trans-allele repression.
Tylosis (focal non-epidermolytic palmoplantar keratoderma) is an autosomal dominant skin disorder that is associated with the… (More)
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2005
2005
K4, K9 and K18 in human histone H3 are targets for biotinylation by biotinidase.
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
Formation of facultative heterochromatin in the absence of HP1.
Facultative heterochromatin is a cytological manifestation of epigenetic mechanisms that regulate gene expression. Constitutive… (More)
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1999
1999
Regulation of keratin 9 in nonpalmoplantar keratinocytes by palmoplantar fibroblasts through epithelial-mesenchymal interactions.
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
Novel mutations in keratin 16 gene underly focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two families.
Keratins K6 and K16 are expressed in suprabasal interfollicular epidermis in wound healing and other pathological conditions… (More)
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1994
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… (More)
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