Duplication of paternal IGF2 or loss of maternal IGF2 imprinting occurs in half of Wilms tumors with various structural WT1 abnormalities (Q81235455)

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7 January 2020

title

Duplication of paternal IGF2 or loss of maternal IGF2 imprinting occurs in half of Wilms tumors with various structural WT1 abnormalities (English)

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2

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Hidenobu Soejima

7

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author name string

Masayuki Haruta

1

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Waka Sugawara

3

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Naoki Watanabe

4

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Shohei Honda

5

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Junjiro Ohshima

6

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Hisaya Nakadate

8

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Hajime Okita

9

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Jun-ichi Hata

10

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Masahiro Fukuzawa

11

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Yasuhiko Kaneko

12

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publication date

1 August 2008

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Genes, Chromosomes and Cancer

7 January 2020

published in

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volume

47

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page(s)

712-727

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issue

8

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Histopathology and prognosis of Wilms tumorResults from the first national wilms' tumor study

7 January 2020

cites work

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7 January 2021

Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome

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7 January 2021

Genomic imprinting at the WT1 gene involves a novel coding transcript (AWT1) that shows deregulation in Wilms' tumours.

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7 January 2021

Treatment of Wilms' tumor. Results of the Third National Wilms' Tumor Study

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7 January 2021

Development of an siRNA-based method for repressing specific genes in renal organ culture and its use to show that the Wt1 tumour suppressor is required for nephron differentiation.

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7 January 2021

Repression of the insulin-like growth factor II gene by the Wilms tumor suppressor WT1

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7 January 2021

Insulin-like growth factor ligands, receptors, and binding proteins in cancer.

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7 January 2021

Sequential WT1 and CTNNB1 mutations and alterations of beta-catenin localisation in intralobar nephrogenic rests and associated Wilms tumours: two case studies

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7 January 2021

Altered expression of members of the IGF-axis in hepatoblastomas

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7 January 2021

A CTCF-binding silencer regulates the imprinted genes AWT1 and WT1-AS and exhibits sequential epigenetic defects during Wilms' tumourigenesis

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7 January 2021

The many facets of the Wilms' tumour gene, WT1

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7 January 2021

WT-1 is required for early kidney development

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7 January 2021

CTNNB1 mutations and overexpression of Wnt/beta-catenin target genes in WT1-mutant Wilms' tumors

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7 January 2021

A clinical overview of WT1 gene mutations

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7 January 2021

Correlation of chromosome abnormalities with presence or absence of WT1 deletions/mutations in Wilms tumor.

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7 January 2021

Mutations/deletions of the WT1 gene, loss of heterozygosity on chromosome arms 11p and 11q, chromosome ploidy and histology in Wilms' tumors in Japan

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7 January 2021

A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

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7 January 2021

WT1 mutations in patients with Denys-Drash syndrome: a novel mutation in exon 8 and paternal allele origin

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7 January 2021

Germline mutations of the POU6F2 gene in Wilms tumors with loss of heterozygosity on chromosome 7p14.

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7 January 2021

Loss of Imprinting of Insulin-Like Growth Factor-II (IGF2) Gene in Distinguishing Specific Biologic Subtypes of Wilms Tumor

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7 January 2021

Wilms' tumour: connecting tumorigenesis and organ development in the kidney

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7 January 2021

An X chromosome gene, WTX, is commonly inactivated in Wilms tumor

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7 January 2021

Twenty-four new cases of WT1 germline mutations and review of the literature: genotype/phenotype correlations for Wilms tumor development

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7 January 2021

Genome-wide loss of heterozygosity analysis of WT1-wild-type and WT1-mutant Wilms tumors

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7 January 2021

Significant reduction of WT1 gene expression, possibly due to epigenetic alteration in Wilms' tumor.

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7 January 2021

Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours

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7 January 2021

WT1 proteins: functions in growth and differentiation

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7 January 2021

Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology

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7 January 2021

Molecular characterization of a 7p15-21 homozygous deletion in a Wilms tumor

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7 January 2021

Promoter hypermethylation of the RASSF1A gene predicts the poor outcome of patients with hepatoblastoma

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7 January 2021

Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancer

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7 January 2021

Duplication of the paternal IGF2 allele in trisomy 11 and elevated expression levels of IGF2 mRNA in congenital mesoblastic nephroma of the cellular or mixed type

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7 January 2021

Association of 11q loss, trisomy 12, and possible 16q loss with loss of imprinting of insulin-like growth factor-II in Wilms tumor

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7 January 2021

Genomic profiling maps loss of heterozygosity and defines the timing and stage dependence of epigenetic and genetic events in Wilms' tumors.

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7 January 2021

Activation of an imprinted allele of the insulin-like growth factor II gene implicated in rhabdomyosarcoma

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7 January 2021

Identifiers

DOI

10.1002/GCC.20572

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7 January 2020

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