FAQ

ICR1 gene

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

Topic mentions per year

Topic mentions per year

2006-2017
012320062017

Related topics

Related topics

3 relations
Congenital ichthyosisICR3 gene

Narrower (1)

ICR4 gene

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
ICR1 gene
Congenital ichthyosis
ICR3 gene
ICR4 gene

Papers overview

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2017
2017
11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver-Russell Syndrome.
The 11p15 region harbors the IGF2/H19 imprinted domain, implicated in fetal and postnatal growth. Silver-Russell syndrome (SRS… (More)
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2017
2017
Fate of methylated/unmethylated H19 imprinting control region after paternal and maternal pronuclear injection
The paternal-allele-specific methylation of the Igf2/H19 imprinting control region (ICR) is established during gametogenesis and… (More)
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2015
2015
Long non-coding RNA 91H contributes to the occurrence and progression of esophageal squamous cell carcinoma by inhibiting IGF2 expression.
Long non-coding RNAs (lncRNAs) have been recently recognized as a major class of regulators in mammalian systems. 91H, a novel… (More)
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2015
2015
Reduced DNA methylation at the PEG3 DMR and KvDMR1 loci in children exposed to alcohol in utero: a South African Fetal Alcohol Syndrome cohort study
Fetal alcohol syndrome (FAS) is a devastating developmental disorder resulting from alcohol exposure during fetal development. It… (More)
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2014
2014
Bimodal regulation of ICR1 levels generates self-organizing auxin distribution.
Auxin polar transport, local maxima, and gradients have become an important model system for studying self-organization. Auxin… (More)
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2010
2010
MBD3 mutations are not responsible for ICR1 hypomethylation in Silver-Russell syndrome.
Silver-Russell syndrome (SRS) is a sporadic and heterogeneous disease that is mainly associated with intrauterine and postnatal… (More)
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Review
2010
Review
2010
Genetic and epigenetic findings in Silver-Russell syndrome.
Silver-Russell syndrome (SRS) is a genetically and clinically heterogeneous disease which is mainly characterized by pre- and… (More)
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2008
2008
ICR1 epimutations in llp15 are restricted to patients with Silver-Russell syndrome features.
(Epi)mutations affecting chromosome llp15 are well known to be associated with growth disturbances. The finding of llp15… (More)
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2007
2007
No evidence for additional imprinting defects in Silver-Russell syndrome patients with maternal uniparental disomy 7 or 11p15 epimutation.
Silver-Russell syndrome (SRS) is mainly characterised by intrauterine and postnatal growth retardation (IUGR and PNGR), asymmetry… (More)
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2006
2006
IGF-II serum levels are normal in children with Silver-Russell syndrome who frequently carry epimutations at the IGF2 locus.
CONTEXT Epigenetic mutations of 11p15 encompassing IGF2 are present in short children with Silver-Russell syndrome (SRS) with… (More)
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