Establishment of a Conditionally Immortalized Wilms Tumor Cell Line with a Homozygous WT1 Deletion within a Heterozygous 11p13 Deletion and UPD Limited to 11p15-Reference-Cited by-同舟云学术

Establishment of a Conditionally Immortalized Wilms Tumor Cell Line with a Homozygous WT1 Deletion within a Heterozygous 11p13 Deletion and UPD Limited to 11p15

Published:2016-05-23 Issue:5 Volume:11 Page:e0155561
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Brandt Artur,Löhers Katharina,Beier Manfred,Leube Barbara,de Torres Carmen,Mora Jaume,Arora Parineeta,Jat Parmjit S.,Royer-Pokora Brigitte

Funder

Deutsche Forschungsgemeinschaft

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference39 articles.

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3. Two molecular subgroups of Wilms' tumors with or without WT1 mutations;V Schumacher;Clin Cancer Res,2003

4. Frequency and heritability of WT1 mutations in nonsyndromic Wilms’ tumor patients: A UK Children’s Cancer Study Group Study;SE Little;J Clin Oncol,2004

5. Clinical relevance of mutations in the Wilms tumor suppressor 1 gene WT1 and the cadherin-associated protein beta1 gene CTNNB1 for patients with Wilms tumors: results of long-term surveillance of 71 patients from International Society of Pediatric Oncology Study 9/Society for Pediatric Oncology;B Royer-Pokora;Cancer,2008

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