Duplication of paternalIGF2 or loss of maternalIGF2 imprinting occurs in half of Wilms tumors with various structuralWT1 abnormalities-Reference-Cited by-同舟云学术

Duplication of paternalIGF2 or loss of maternalIGF2 imprinting occurs in half of Wilms tumors with various structuralWT1 abnormalities

Published:2008 Issue:8 Volume:47 Page:712-727
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosom. Cancer

Author:

Haruta Masayuki,Arai Yasuhito,Sugawara Waka,Watanabe Naoki,Honda Shohei,Ohshima Junjiro,Soejima Hidenobu,Nakadate Hisaya,Okita Hajime,Hata Jun-ichi,Fukuzawa Masahiro,Kaneko Yasuhiko

Publisher

Wiley

Subject

Cancer Research,Genetics

Reference42 articles.

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

2. Molecular subtypes and phenotypic expression of Beckwith–Wiedemann syndrome

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

4. Treatment of Wilms' tumor. Results of the third national Wilms' tumor study

5. 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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