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KDM5C wt Allele
Known as:
XE169
, MRXSCJ
, JARID1C
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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…
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National Institutes of Health
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Related topics
Related topics
6 relations
Broader (1)
KDM5C gene
Oxidation-Reduction
Post-Translational Protein Processing
Transcriptional Regulation
Xp11.22-p11.21
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Epigenetic Regulation of Angiogenesis by JARID1B-Induced Repression of HOXA5
Christian Fork
,
Lunda Gu
,
+12 authors
R. Brandes
Arteriosclerosis, Thrombosis and Vascular Biology
2015
Corpus ID: 19555403
Objective— Altering endothelial biology through epigenetic modifiers is an attractive novel concept, which is, however, just in…
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2015
2015
Aging induced cortical drive alterations during sleep in rats
J. Ciric
,
K. Lazić
,
J. Petrović
,
Aleksandar Kalauzi
,
J. Saponjic
Mechanisms of Ageing and Development
2015
Corpus ID: 41124329
2014
2014
REM sleep diversity following the pedunculopontine tegmental nucleus lesion in rat
J. Petrović
,
K. Lazić
,
Aleksandar Kalauzi
,
J. Saponjic
Behavioural Brain Research
2014
Corpus ID: 22124210
2008
2008
Repression of Smad3 activity by histone demethylase SMCX/JARID1C.
Tae-Dong Kim
,
Sook Shin
,
R. Janknecht
Biochemical and Biophysical Research…
2008
Corpus ID: 19709233
2008
2008
Backbone and sidechain 1H, 13C and 15N resonance assignments of the Bright/ARID domain from the human JARID1C (SMCX) protein
C. Koehler
,
S. Bishop
,
+4 authors
Linda J. Ball
Biomolecular NMR Assignments
2008
Corpus ID: 36228372
We have assigned 1H, 15N and 13C resonances of the Bright/ARID DNA-binding domain from the human JARID1C protein, a newly…
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Review
2006
Review
2006
[Non-specific X-linked mental retardation].
F. Martínez-Castellano
Revista de neurología (Ed. impresa)
2006
Corpus ID: 7304007
INTRODUCTION Non-specific mental retardation is defined by the absence of somatic, neurological, biochemical or behavioural…
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Highly Cited
1994
Highly Cited
1994
Isolation and characterization of XE169, a novel human gene that escapes X-inactivation.
J. Wu
,
J. Ellison
,
E. Salido
,
P. Yen
,
T. Mohandas
,
L. Shapiro
Human Molecular Genetics
1994
Corpus ID: 32581579
Overlapping cDNA clones for a novel human X-linked gene, XE169, have been isolated and characterized. The composite cDNA sequence…
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Highly Cited
1992
Highly Cited
1992
Biochemical and behavioral effects of a sensorimotor cortex injury in rats pretreated with the noradrenergic neurotoxin DSP-4.
M. Boyeson
,
T. R. Callister
,
J. Cavazos
Behavioral Neuroscience
1992
Corpus ID: 19675247
The role of the noradrenergic (NE) system in recovery of motor function after sensorimotor cortex (SMCX) injury was investigated…
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1992
1992
Localization of non-specific X-linked mental retardation genes.
B. Kerr
,
A. Gedeon
,
J. Mulley
,
G. Turner
American journal of medical genetics
1992
Corpus ID: 40264168
Gene localization was determined by linkage analysis in 5 families with non-specific X-linked mental retardation (MRX) and were…
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Review
1991
Review
1991
Non-specific X linked mental retardation.
B. Kerr
,
G. Turner
,
J. Mulley
,
A. Gedeon
,
M. Partington
Journal of Medical Genetics
1991
Corpus ID: 35878549
Non-specific X linked mental retardation (MRX) is mental retardation in persons of normal physical appearance who have no…
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