Skip to search formSkip to main contentSkip to account menu

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… 
National Institutes of Health

Related topics

Related topics

6 relations

Broader (1)

KDM5C gene
Oxidation-ReductionPost-Translational Protein ProcessingTranscriptional RegulationXp11.22-p11.21

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Histone demethylase JARID1C inactivation triggers genomic instability in sporadic renal cancer.
2015
2015
Aging induced cortical drive alterations during sleep in rats
2014
2014
REM sleep diversity following the pedunculopontine tegmental nucleus lesion in rat
2010
2010
The JmjN Domain of Jhd 2 Is Important for Its Protein Stability , and the Plant Homeodomain ( PHD ) Finger Mediates Its Chromatin Association Independent of H 3 K 4 Methylation *
Histone lysine methylation is a dynamic process that plays an important role in regulating chromatin structure and gene… 
2009
2009
Exon-level gene expression analyses of primary neuroblastoma improves risk prediction and identifies JARID1C as a candidate target
Neuroblastoma (NB), the most common solid tumor of childhood, is characterized by a remarkable heterogeneity of patients' courses… 
2008
2008
Backbone and sidechain 1H, 13C and 15N resonance assignments of the Bright/ARID domain from the human JARID1C (SMCX) protein
We have assigned 1H, 15N and 13C resonances of the Bright/ARID DNA-binding domain from the human JARID1C protein, a newly… 
Review
2006
Review
2006
[Non-specific X-linked mental retardation].
INTRODUCTION Non-specific mental retardation is defined by the absence of somatic, neurological, biochemical or behavioural… 
2005
2005
JARID1C, a novel gene involved in X-linked mental retardation, is frequently mutated
2004
2004
Expression pattern of X-linked genes in sex chromosome aneuploid bovine cells
Expression of the X-inactive specific transcript (XIST) gene is a prerequisite step for dosage compensation in mammals… 
Highly Cited
1994
Highly Cited
1994
Isolation and characterization of XE169, a novel human gene that escapes X-inactivation.
Overlapping cDNA clones for a novel human X-linked gene, XE169, have been isolated and characterized. The composite cDNA sequence… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)