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KIAA2022 gene

Known as: KIAA2022, MRX98, XPN 
 
National Institutes of Health

Papers overview

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2016
2016
Background Mutations in the KIAA2022 gene have been reported in male patients with X-linked intellectual disability, and related… Expand
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2016
2016
Abstract Our previous work showed that loss of the KIAA2022 gene protein results in intellectual disability with language… Expand
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2015
2015
Next-generation sequencing has enabled the screening for a causative mutation in X-linked intellectual disability (XLID). We… Expand
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2014
2014
Numerical simulations are conducted to study the current-matching effect and operation mechanisms in and to design the optimized… Expand
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2013
2013
Existence of a discrete new X-linked intellectual disability (XLID) syndrome due to KIAA2022 deficiency was questioned by… Expand
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2012
2012
Abstract. Peroxynitrates are responsible for global scale transport of reactive nitrogen. Recent laboratory observations suggest… Expand
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Highly Cited
2011
Highly Cited
2011
BackgroundSimultaneous measurement of gene expression on a genomic scale can be accomplished using microarray technology or by… Expand
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2010
2010
Background Inferring Gene Regulatory Networks (GRNs) from time course microarray data suffers from the dimensionality problem… Expand
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2004
2004
We introduce crowded-field integral field (3D) spectrophotometry as a useful technique for the study of resolved stellar… Expand
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2004
2004
Background: Mental retardation (MR) affects 2–3% of the human population and some of these cases are genetically determined… Expand
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