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ICR1 gene
Known as:
H19 ICR
, ICR1
, H19/IGF2-IMPRINTING CONTROL REGION
Â
(More)
Â
National Institutes of Health
Topic mentions per year
Topic mentions per year
2006-2017
0
1
2
3
2006
2017
Related topics
Related topics
3 relations
Congenital ichthyosis
ICR3 gene
Narrower (1)
ICR4 gene
Related mentions per year
Related mentions per year
1936-2018
1940
1960
1980
2000
2020
ICR1 gene
Congenital ichthyosis
ICR3 gene
ICR4 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver-Russell Syndrome.
Walid Abi Habib
,
Frédéric Brioude
,
+8 authors
Irène Netchine
Human mutation
2017
The 11p15 region harbors the IGF2/H19 imprinted domain, implicated in fetal and postnatal growth. Silver-Russell syndrome (SRS…Â
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2017
2017
Fate of methylated/unmethylated H19 imprinting control region after paternal and maternal pronuclear injection
Asami Oji
,
Tomojiro Amano
,
+4 authors
Tomoko M. Nakanishi
Experimental animals
2017
The paternal-allele-specific methylation of the Igf2/H19 imprinting control region (ICR) is established during gametogenesis and…Â
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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.
Tianyi Gao
,
B. He
,
+5 authors
Shu-Kui Wang
Molecular carcinogenesis
2015
Long non-coding RNAs (lncRNAs) have been recently recognized as a major class of regulators in mammalian systems. 91H, a novel…Â
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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
Matshane L. Masemola
,
Lize van der Merwe
,
Zané Lombard
,
Denis Viljoen
,
Michéle Ramsay
Front. Genet.
2015
Fetal alcohol syndrome (FAS) is a devastating developmental disorder resulting from alcohol exposure during fetal development. It…Â
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2014
2014
Bimodal regulation of ICR1 levels generates self-organizing auxin distribution.
Ora Hazak
,
Uri Obolski
,
Tomáš Prát
,
Jiřà Friml
,
Lilach Hadany
,
Shaul Yalovsky
Proceedings of the National Academy of Sciences…
2014
Auxin polar transport, local maxima, and gradients have become an important model system for studying self-organization. Auxin…Â
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2010
2010
MBD3 mutations are not responsible for ICR1 hypomethylation in Silver-Russell syndrome.
Nadine Bachmann
,
Sabrina Spengler
,
G. Binder
,
Thomas Eggermann
European journal of medical genetics
2010
Silver-Russell syndrome (SRS) is a sporadic and heterogeneous disease that is mainly associated with intrauterine and postnatal…Â
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Review
2010
Review
2010
Genetic and epigenetic findings in Silver-Russell syndrome.
Thomas Eggermann
,
Matthias Begemann
,
Sabrina Spengler
,
Carmen M Schröder
,
Ulrike Kordass
,
G. Binder
Pediatric endocrinology reviews : PER
2010
Silver-Russell syndrome (SRS) is a genetically and clinically heterogeneous disease which is mainly characterized by pre- and…Â
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2008
2008
ICR1 epimutations in llp15 are restricted to patients with Silver-Russell syndrome features.
Thomas Eggermann
,
Esther Meyer
,
Ahmet Okay Çağlayan
,
Munis Dundar
,
Nadine Schoenherr
Journal of pediatric endocrinology & metabolism…
2008
(Epi)mutations affecting chromosome llp15 are well known to be associated with growth disturbances. The finding of llp15…Â
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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.
Nadine Schoenherr
,
Esther Meyer
,
G. Binder
,
Hartmut A. Wollmann
,
Thomas Eggermann
Journal of pediatric endocrinology & metabolism…
2007
Silver-Russell syndrome (SRS) is mainly characterised by intrauterine and postnatal growth retardation (IUGR and PNGR), asymmetry…Â
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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.
G. Binder
,
A-K Seidel
,
+4 authors
Thomas Eggermann
The Journal of clinical endocrinology and…
2006
CONTEXT Epigenetic mutations of 11p15 encompassing IGF2 are present in short children with Silver-Russell syndrome (SRS) with…Â
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