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ICR1 gene

Known as: H19 ICR, ICR1, H19/IGF2-IMPRINTING CONTROL REGION 
 
National Institutes of Health

Papers overview

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2015
2015
Long non‐coding RNAs (lncRNAs) have been recently recognized as a major class of regulators in mammalian systems. 91H, a novel… Expand
Highly Cited
2014
Highly Cited
2014
Isolated gain of methylation (GOM) at the IGF2/H19 imprinting control region 1 (ICR1) accounts for about 10% of patients with BWS… Expand
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2014
2014
The Beckwith-Wiedemann syndrome is caused by disturbed imprinting of genes at 11p15.5. Routine diagnostic testing for Beckwith… Expand
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Highly Cited
2013
Highly Cited
2013
Background: Beckwith-Wiedemann syndrome (BWS) is an overgrowth syndrome associated with an increased risk of pediatric tumors… Expand
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2012
2012
BackgroundLoss of methylation (LOM) at imprinting control region (ICR) 1 or LOM at ICR 2 on chromosome 11p15 in leucocyte DNA is… Expand
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Highly Cited
2010
Highly Cited
2010
UNLABELLED Many genes exhibiting genomic imprinting, parent-of-origin differences in gene expression, are involved in regulating… Expand
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2008
2008
(Epi)mutations affecting chromosome llp15 are well known to be associated with growth disturbances. The finding of llp15… Expand
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2008
2008
ROPs/RACs are the only known signaling Ras superfamily small GTPases in plants. As such they have been suggested to function as… Expand
Highly Cited
2006
Highly Cited
2006
Introduction: Silver-Russell syndrome (SRS; also know as Russell-Silver syndrome) is a heterogeneous syndrome which is… Expand
Highly Cited
2006
Highly Cited
2006
CONTEXT Epigenetic mutations of 11p15 encompassing IGF2 are present in short children with Silver-Russell syndrome (SRS) with… Expand