Sequential WT1 and CTNNB1 mutations and alterations of -catenin localisation in intralobar nephrogenic rests and associated Wilms tumours: two case studies-Reference-Cited by-同舟云学术

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

Published:2006-11-14 Issue:9 Volume:60 Page:1013-1016
ISSN:0021-9746
Container-title:Journal of Clinical Pathology
language:en
Short-container-title:Journal of Clinical Pathology

Author:

Fukuzawa R.,Heathcott R. W,More H. E,Reeve A. E

Publisher

BMJ

Subject

General Medicine,Pathology and Forensic Medicine

Cited by 56 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. In utero tumor development and identification of CTNNB1 mutation in a newborn case of ossifying renal tumor of infancy;Pediatric Blood & Cancer;2024-01-12

2. Genetic and epigenetic features of bilateral Wilms tumor predisposition in patients from the Children’s Oncology Group AREN18B5-Q;Nature Communications;2023-12-18

3. The Genetic and Epigenetic Features of Bilateral Wilms Tumor Predisposition: A Report from the Children's Oncology Group AREN18B5-Q Study;2023-03-16

4. WT1 regulates expression of DNA repair gene Neil3 during nephrogenesis;American Journal of Physiology-Renal Physiology;2023-03-01

5. Somatic, Genetic and Epigenetic Changes in Nephrogenic Rests and Their Role in the Transformation to Wilms Tumors, a Systematic Review;Cancers;2023-02-21

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