About: Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor

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About: Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor Goto Sponge NotDistinct Permalink

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scientific article published on 27 February 2009

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2009 (ast) наукова стаття, опублікована в лютому 2009 (uk) scientific article published on 27 February 2009 (en) مقالة علمية نشرت في 27 فبراير 2009 (ar)
publication date	wds:Q37416973-E0509393-E266-4494-BF68-192479E4245C
publication date	2009-02-27 00:00:00Z (xsd:dateTime)
author name string	wds:Q37416973-07AC6C9D-1B19-4AAD-BF1F-DCED469FBDDD wds:Q37416973-0E68478D-6B5B-4201-A115-8CBC1CBB9EAB wds:Q37416973-2B3D455A-C5D0-472B-8B47-EF018A901FED wds:Q37416973-2F2D5E85-B819-472A-B2E9-3D4712CE73C1 wds:Q37416973-35DF5F04-41EC-426D-9AE9-AD0A87335725 wds:Q37416973-7618DF1C-9072-4C80-9AAE-552F19983848 wds:Q37416973-895DA371-8D25-49E9-9AC6-6AE51BF18165 wds:Q37416973-C9D8AA18-F915-4601-8EBB-814F777CCCD3 wds:Q37416973-D1ED1C25-CFE0-4509-9E12-BDB153E499D1 wds:Q37416973-F552AB2A-DA11-4832-9F68-27F84D51E846
author name string	Agostina De Crescenzo Andrea Riccio Silvia Russo Lidia Larizza Angela Sparago Flavia Cerrato Maria Vittoria Cubellis Valentina Citro Giovanni Battista Ferrero Gaetano Verde
rdfs:label	Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor (en) Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor (nl) Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor (ast)
skos:prefLabel	Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor (en) Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor (nl) Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor (ast)
name	Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor (en) Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor (nl) Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor (ast)
author	wds:Q37416973-873E5E62-5AF3-4D68-A48A-5C240C228910
author	Margherita Cirillo Silengo
title	wds:Q37416973-0BA7CB47-286A-4A89-9CC1-D6390675F717
title	Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor (en)
page(s)	wds:Q37416973-60C3EC9D-3B52-42A0-B8C3-A7C4CA92C198
page(s)	1-9
instance of	wds:Q37416973-362CF110-4E16-4B59-AAE1-7DA6E494CE06 wds:Q37416973-7706198a-d8b5-4c8e-bd10-7b49b7b50d58
instance of	review article scholarly article
main subject	wds:Q37416973-247AE5BD-4B06-4432-A1E6-5FD7C050C723
main subject	Beckwith-Wiedemann syndrome
PubMed ID	wds:Q37416973-385B9B86-A6F7-4CE4-B904-DAC4AC7D62C8
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/19293570
PubMed ID	19293570
published in	wds:Q37416973-028C6E3D-179D-4496-ADC6-4BCA4AC5B18B
published in	Endocrine development
volume	wds:Q37416973-47E2ED31-A1CA-4E65-8437-37E28FE5ACB1
volume	14
DOI	wds:Q37416973-EBCEB573-9AE0-4890-BA82-967144893906
DOI	http://dx.doi.org/10.1159/000207461
DOI	10.1159/000207461
ResearchGate publication ID	wds:Q37416973-53A6EA39-8C47-4008-8F36-D0FA531255A5
ResearchGate publication ID	24207690
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37416973
is cites work of	Epigenetic heredity of human height (Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome Longitudinal epigenetic drift in mice perinatally exposed to lead. CRISPR Cas9-guided chromatin immunoprecipitation identifies miR483 as an epigenetic modulator of IGF2 imprinting in tumors Gender-specific methylation differences in relation to prenatal exposure to cigarette smoke Evidence for anticipation in Beckwith-Wiedemann syndrome Wilms tumor suppressor, WT1, suppresses epigenetic silencing of the β-catenin gene An 11p15 imprinting centre region 2 deletion in a family with Beckwith Wiedemann syndrome provides insights into imprinting control at CDKN1C. Beckwith-Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques Fetal growth patterns in Beckwith-Wiedemann syndrome. A novel large deletion of the ICR1 region including H19 and putative enhancer elements (Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome: a paradigm for genomic medicine. Prevalence of beckwith-wiedemann syndrome in North West of Italy α-Fetoprotein assay on dried blood spot for hepatoblastoma screening in children with overgrowth-cancer predisposition syndromes Association of genomic instability, and the methylation status of imprinted genes and mismatch-repair genes, with neural tube defects Therapeutic Targeting of the IGF Axis Altered methylations of H19, Snrpn, Mest and Peg3 are reversible by developmental reprogramming in kidney tissue of ICSI-derived mice Microarray analysis reveals higher gestational folic Acid alters expression of genes in the cerebellum of mice offspring-a pilot study Lentivirus-mediated RNA interference targeting the H19 gene inhibits cell proliferation and apoptosis in human choriocarcinoma cell line JAR Upregulation of imprinted genes in mice: an insight into the intensity of gene expression and the evolution of genomic imprinting Epigenetic signatures may explain the relationship between socioeconomic position and risk of mental illness: preliminary findings from an urban community-based sample. Addition of H19 'loss of methylation testing' for Beckwith-Wiedemann syndrome (BWS) increases the diagnostic yield. Beckwith-Weidemann syndrome with IC2 (KvDMR1) hypomethylation defect: a novel mutation.
is cites work of	wds:Q37317003-268CDD8E-765C-4F85-9643-0E6E9E64C470 wds:Q85204433-5796C0F2-D14D-447D-A01B-A526DE7E896F wds:Q33798311-F2E0AB88-17F8-438E-9E35-58300801BF93 wds:Q41696623-709E07D0-711F-4250-8B82-397BBD8EDCFC

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