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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… 
National Institutes of Health

Papers overview

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2015
2015
Objective— Altering endothelial biology through epigenetic modifiers is an attractive novel concept, which is, however, just in… 
2008
2008
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
INTRODUCTION Non-specific mental retardation is defined by the absence of somatic, neurological, biochemical or behavioural… 
Highly Cited
1994
Highly Cited
1994
Overlapping cDNA clones for a novel human X-linked gene, XE169, have been isolated and characterized. The composite cDNA sequence… 
Highly Cited
1992
Highly Cited
1992
The role of the noradrenergic (NE) system in recovery of motor function after sensorimotor cortex (SMCX) injury was investigated… 
1992
1992
Gene localization was determined by linkage analysis in 5 families with non-specific X-linked mental retardation (MRX) and were… 
Review
1991
Review
1991
Non-specific X linked mental retardation (MRX) is mental retardation in persons of normal physical appearance who have no…