KDM5C wt Allele

Known as: XE169, MRXSCJ, JARID1C 
Human KDM5C wild-type allele is located within Xp11.22-p11.21 and is approximately 34 kb in length. This allele, which encodes lysine-specific… (More)
National Institutes of Health

Papers overview

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Highly Cited
2009
Highly Cited
2009
The identification of histone methyltransferases and demethylases has uncovered a dynamic methylation system needed to modulate… (More)
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2009
2009
Extensive interspecific genetic introgression is often reported, and appraising its genomic impact can serve to determine whether… (More)
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Highly Cited
2008
Highly Cited
2008
We describe a nondysmorphic patient with developmental delay and autism spectrum disorder who has a missense mutation in the… (More)
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Highly Cited
2007
Highly Cited
2007
Gene transcription is critically influenced by chromatin structure and the modification status of histone tails. Methylation of… (More)
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Highly Cited
2007
Highly Cited
2007
Histone methylation regulates chromatin structure and transcription. The recently identified histone demethylase lysine-specific… (More)
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Highly Cited
2005
Highly Cited
2005
Escape from X inactivation results in expression of genes embedded within inactive chromatin, suggesting the existence of… (More)
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Highly Cited
2005
Highly Cited
2005
In families with nonsyndromic X-linked mental retardation (NS-XLMR), >30% of mutations seem to cluster on proximal Xp and in the… (More)
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Highly Cited
2002
Highly Cited
2002
A major question is whether genes encoded on the sex chromosomes act directly in non-gonadal tissues to cause sex differences in… (More)
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Highly Cited
1999
Highly Cited
1999
Cytogenetic and molecular deletion analyses of azoospermic and oligozoospermic males have suggested the existence of AZoospermia… (More)
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Highly Cited
1994
Highly Cited
1994
A new gene, designated Smcx, was cloned from the mouse X chromosome by its homology to the Y located gene Smcy. Using direct in… (More)
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