Chemotherapy and terminal skeletal muscle differentiation in WT1- mutant Wilms tumors-Reference-Cited by-同舟云学术

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Chemotherapy and terminal skeletal muscle differentiation in WT1- mutant Wilms tumors

Published:2018-03-15 Issue:4 Volume:7 Page:1359-1368
ISSN:2045-7634
Container-title:Cancer Medicine
language:en
Short-container-title:Cancer Med

Author:

Royer-Pokora Brigitte¹^ORCID,Beier Manfred¹,Brandt Artur¹,Duhme Constanze¹,Busch Maike¹,de Torres Carmen²,Royer Hans-Dieter¹,Mora Jaume²

Affiliation:

1. Institute of Human Genetics; Heinrich-Heine University; Düsseldorf D-40225 Germany

2. Department of Oncology; Hospital Sant Joan de Deu; Barcelona 08950 Spain

Funder

Deutsche Forschungsgemeinschaft

“Band of parents” grant in support of the developmental tumor biology laboratory, Hospital Sant Joan de Déu, Barcelona

Publisher

Wiley

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology

Reference29 articles.

1. Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology;Schumacher;Proc. Natl Acad. Sci. USA,1997

2. Frequent association of beta-catenin and WT1 mutations in Wilms tumors;Maiti;Cancer Res.,2000

3. 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;Royer-Pokora;Cancer,2008

4. Risk stratification for Wilms tumor: current approach and future directions;Dome;Am. Soc. Clin. Oncol. Educ. Book,2014

5. Advances in Wilms Tumor treatment and biology: progress through international collaboration;Dome;J. Clin. Oncol.,2015

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