A Children's Oncology Group and TARGET initiative exploring the genetic landscape of Wilms tumor-Reference-Cited by-同舟云学术

A Children's Oncology Group and TARGET initiative exploring the genetic landscape of Wilms tumor

Published:2017-08-21 Issue:10 Volume:49 Page:1487-1494
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Gadd Samantha,Huff Vicki,Walz Amy L,Ooms Ariadne H A G,Armstrong Amy E,Gerhard Daniela S,Smith Malcolm A^ORCID,Auvil Jaime M Guidry,Meerzaman Daoud,Chen Qing-Rong,Hsu Chih Hao,Yan Chunhua,Nguyen Cu,Hu Ying,Hermida Leandro C,Davidsen Tanja,Gesuwan Patee,Ma Yussanne,Zong Zusheng,Mungall Andrew J^ORCID,Moore Richard A,Marra Marco A,Dome Jeffrey S,Mullighan Charles G^ORCID,Ma Jing,Wheeler David A,Hampton Oliver A,Ross Nicole,Gastier-Foster Julie M,Arold Stefan T,Perlman Elizabeth J^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.3940.pdf

Reference79 articles.

1. Gadd, S. et al. Clinically relevant subsets identified by gene expression patterns support a revised ontogenic model of Wilms tumor: a Children's Oncology Group Study. Neoplasia 14, 742–756 (2012).

2. Torrezan, G.T. et al. Recurrent somatic mutation in DROSHA induces microRNA profile changes in Wilms tumour. Nat. Commun. 5, 4039 (2014).

3. Wegert, J. et al. Mutations in the SIX1/2 pathway and the DROSHA/DGCR8 miRNA microprocessor complex underlie high-risk blastemal type Wilms tumors. Cancer Cell 27, 298–311 (2015).

4. Rakheja, D. et al. Somatic mutations in DROSHA and DICER1 impair microRNA biogenesis through distinct mechanisms in Wilms tumours. Nat. Commun. 2, 4802 (2014).

5. Beckwith, J.B. & Palmer, N.F. Histopathology and prognosis of Wilms tumors: results from the First National Wilms' Tumor Study. Cancer 41, 1937–1948 (1978).

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