Absence of oncogenic canonical pathway mutations in aggressive pediatric rhabdoid tumors-Reference-Cited by-同舟云学术

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Absence of oncogenic canonical pathway mutations in aggressive pediatric rhabdoid tumors

Published:2012-09-19 Issue:7 Volume:59 Page:1155-1157
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr. Blood Cancer

Author:

Kieran Mark W.,Roberts Charles W.M.,Chi Susan N.,Ligon Keith L.,Rich Benjamin E.,MacConaill Laura E.,Garraway Levi A.,Biegel Jaclyn A.

Funder

National Brain Tumor Society

Cure ATRT Foundation

NIH

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pbc.24315/fullpdf

Reference25 articles.

1. The role of SMARCB1/INI1 in development of rhabdoid tumor;Roberts;Cancer Biol Ther,2009

2. INI1-deficient tumors: Diagnostic features and molecular genetics;Hollmann;Am J Surg Pathol,2011

3. Intensive multimodality treatment for children with newly diagnosed CNS atypical teratoid rhabdoid tumor;Chi;J Clin Oncol,2009

4. Malignant rhabdoid tumours of the kidney (MRTKs), registered on recent SIOP protocols from 1993 to 2005: A report of the SIOP renal tumour study group;van den Heuvel-Eibrink;Pediatr Blood Cancer,2011

5. hSNF5/INI1-deficient tumours and rhabdoid tumours are convergent but not fully overlapping entities;Bourdeaut;J Pathol,2007

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