Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor.
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Gender-specific methylation differences in relation to prenatal exposure to cigarette smokeAn 11p15 imprinting centre region 2 deletion in a family with Beckwith Wiedemann syndrome provides insights into imprinting control at CDKN1C.CRISPR Cas9-guided chromatin immunoprecipitation identifies miR483 as an epigenetic modulator of IGF2 imprinting in tumors.Longitudinal epigenetic drift in mice perinatally exposed to lead.Addition of H19 'loss of methylation testing' for Beckwith-Wiedemann syndrome (BWS) increases the diagnostic yield.Epigenetic heredity of human height.Upregulation of imprinted genes in mice: an insight into the intensity of gene expression and the evolution of genomic imprinting.Lentivirus-mediated RNA interference targeting the H19 gene inhibits cell proliferation and apoptosis in human choriocarcinoma cell line JARWilms tumor suppressor, WT1, suppresses epigenetic silencing of the β-catenin gene.Microarray analysis reveals higher gestational folic Acid alters expression of genes in the cerebellum of mice offspring-a pilot study.A novel large deletion of the ICR1 region including H19 and putative enhancer elementsAssociation of genomic instability, and the methylation status of imprinted genes and mismatch-repair genes, with neural tube defects.(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndromeEpigenetic signatures may explain the relationship between socioeconomic position and risk of mental illness: preliminary findings from an urban community-based sample.Evidence for anticipation in Beckwith-Wiedemann syndrome.(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome: a paradigm for genomic medicine.Fetal growth patterns in Beckwith-Wiedemann syndrome.Altered methylations of H19, Snrpn, Mest and Peg3 are reversible by developmental reprogramming in kidney tissue of ICSI-derived mice.Beckwith-Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques.Prevalence of beckwith-wiedemann syndrome in North West of Italy
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P2860
Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 27 February 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Inherited and Sporadic Epimuta ...... ann syndrome and Wilms' tumor.
@en
Inherited and Sporadic Epimuta ...... ann syndrome and Wilms' tumor.
@nl
type
label
Inherited and Sporadic Epimuta ...... ann syndrome and Wilms' tumor.
@en
Inherited and Sporadic Epimuta ...... ann syndrome and Wilms' tumor.
@nl
prefLabel
Inherited and Sporadic Epimuta ...... ann syndrome and Wilms' tumor.
@en
Inherited and Sporadic Epimuta ...... ann syndrome and Wilms' tumor.
@nl
P2093
P356
P1476
Inherited and Sporadic Epimuta ...... ann syndrome and Wilms' tumor.
@en
P2093
Agostina De Crescenzo
Andrea Riccio
Angela Sparago
Flavia Cerrato
Gaetano Verde
Giovanni Battista Ferrero
Lidia Larizza
Maria Vittoria Cubellis
Silvia Russo
Valentina Citro
P356
10.1159/000207461
P577
2009-02-27T00:00:00Z