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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… Expand
National Institutes of Health

Papers overview

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Highly Cited
2014
Highly Cited
2014
VHL is mutated in the majority of patients with clear cell renal cell carcinoma (ccRCC), with conflicting clinical relevance… Expand
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Review
2009
Review
2009
Alterations in RNA levels are frequently reported in brain of subjects diagnosed with autism, schizophrenia, depression, and… Expand
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Highly Cited
2008
Highly Cited
2008
Jarid1c, an X-linked gene coding for a histone demethylase, plays an important role in brain development and function. Notably… Expand
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Highly Cited
2007
Highly Cited
2007
Histone methylation regulates chromatin structure and transcription. The recently identified histone demethylase lysine-specific… Expand
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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… Expand
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Highly Cited
2006
Highly Cited
2006
X‐linked mental retardation (XLMR) is a heterogeneous disorder that affects approximately 2 in 1000 males. JARID1C/SMCX is… Expand
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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… Expand
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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… Expand
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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… Expand
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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… Expand
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