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

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作者： Masayuki,Haruta ^[1] ; Yasuhito,Arai ; Waka,Sugawara ; Naoki,Watanabe ; Shohei,Honda ; Junjiro,Ohshima ; Hidenobu,Soejima ; Hisaya,Nakadate ; Hajime,Okita ; Jun-ichi,Hata ; Masahiro,Fukuzawa ; Yasuhiko,Kaneko

作者单位： Department of Cancer Diagnosis, Research Institute for Clinical Oncology, Saitama Cancer Center, Ina, Saitama, Japan. ^[1]

主题词 DNA甲基化(DNA Methylation);女(雌)性(Female);基因组印迹(Genomic Imprinting);人类(Humans);胰岛素样生长因子Ⅱ(Insulin-Like Growth Factor II);男(雄)性(Male);突变(Mutation);WT1蛋白质类(WT1 Proteins);Wilms瘤(Wilms Tumor);β连环素(beta Catenin)

DOI 10.1002/gcc.20572

PMID 18464243

发布时间 2008-06-09

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准确一般字义偏差语意偏离译文作用小提交

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Genes, chromosomes & cancer

2008年47卷8期

712-27页

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

Genes, chromosomes & cancer

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Genes, chromosomes & cancer

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

Genes, chromosomes & cancer

相似文献

Genes, chromosomes & cancer

相关期刊

检索历史清除