Genomic imprinting and cancer; new paradigms in the genetics of neoplasia. (Q34232354)

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6 November 2019

review article

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title

Genomic imprinting and cancer; new paradigms in the genetics of neoplasia (English)

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6 November 2019

P N Schofield

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6 November 2019

J A Joyce

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6 November 2019

W K Lam

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6 November 2019

V Grandjean

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6 November 2019

E R Maher

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6 November 2019

publication date

1 March 2001

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6 November 2019

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6 November 2019

volume

120

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6 November 2019

issue

1-3

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6 November 2019

page(s)

151-160

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Analysis of CDKN1C in Beckwith Wiedemann syndrome.

6 November 2019

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Paternal origin of 11p15 duplications in the Beckwith-Wiedemann syndrome. A new case and review of the literature

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Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway

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Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome

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Deletion of a silencer element in Igf2 results in loss of imprinting independent of H19.

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Loss of imprinting in normal tissue of colorectal cancer patients with microsatellite instability

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Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms' tumorigenesis and methylation hyper-dependence of H19 imprinting

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Mtr1, a novel biallelically expressed gene in the center of the mouse distal chromosome 7 imprinting cluster, is a member of the Trp gene family

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Methylation sequencing analysis refines the region of H19 epimutation in Wilms tumor

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7 January 2021

Increased IGF-II protein affects p57kip2 expression in vivo and in vitro: implications for Beckwith-Wiedemann syndrome

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7 January 2021

Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors

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Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma

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Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome

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Isolated hemihyperplasia (hemihypertrophy): Report of a prospective multicenter study of the incidence of neoplasia and review

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Switch from monoallelic to biallelic human IGF2 promoter methylation during aging and carcinogenesis

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7 January 2021

Cancer epigenetics comes of age

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7 January 2021

Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome

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7 January 2021

Genomic imprinting and cancer

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7 January 2021

Biallelic expression of the H19 and IGF2 genes in hepatocellular carcinoma

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7 January 2021

Low Frequency of p57KIP2 Mutation in Beckwith-Wiedemann Syndrome

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7 January 2021

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

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7 January 2021

The imprinted antisense RNA at the Igf2r locus overlaps but does not imprint Mas1

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7 January 2021

Beckwith-Wiedemann syndrome: imprinting in clusters revisited

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7 January 2021

Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15

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7 January 2021

LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids

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7 January 2021

Somatic overgrowth associated with overexpression of insulin-like growth factor II.

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7 January 2021

Epigenetic lesions at the H19 locus in Wilms' tumour patients

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7 January 2021

Genomic imprinting of IGF2 and H19 in human meningiomas

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7 January 2021

Insulin-like Growth Factor II Is Focally Up-regulated and Functionally Involved as a Second Signal for Oncogene-induced Tumorigenesis

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7 January 2021

Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

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7 January 2021

Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors

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Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse

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7 January 2021

Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Gain of imprinting at chromosome 11p15: A pathogenetic mechanism identified in human hepatocarcinomas

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7 January 2021

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

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7 January 2021

Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes

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7 January 2021

Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

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7 January 2021

Hypermethylation of the death-associated protein (DAP) kinase promoter and aggressiveness in stage I non-small-cell lung cancer

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7 January 2021

Human p57(KIP2) defines a new imprinted domain on chromosome 11p but is not a tumour suppressor gene in Wilms tumour

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7 January 2021

Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor

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7 January 2021

Altered transcriptional regulation of the insulin-like growth factor 2 gene in human hepatocellular carcinoma

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7 January 2021

Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome

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7 January 2021

Gene expression profiles in normal and cancer cells

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7 January 2021

10.1016/S0378-4274(01)00294-6

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11323172%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11323172%20AND%20SRC:MED&resulttype=core&format=json