TP53 alterations in Wilms tumour represent progression events with strong intratumour heterogeneity that are closely linked but not limited to anaplasia-Reference-Cited by-同舟云学术

TP53 alterations in Wilms tumour represent progression events with strong intratumour heterogeneity that are closely linked but not limited to anaplasia

Published:2017-08-14 Issue:4 Volume:3 Page:234-248
ISSN:2056-4538
Container-title:The Journal of Pathology: Clinical Research
language:en
Short-container-title:J Path: Clin Res

Author:

Wegert Jenny¹,Vokuhl Christian²,Ziegler Barbara¹,Ernestus Karen³,Leuschner Ivo²,Furtwängler Rhoikos⁴,Graf Norbert⁴,Gessler Manfred¹⁵^ORCID

Affiliation:

1. Theodor-Boveri-Institute/Biocenter, Developmental Biochemistry; Wuerzburg University; Wuerzburg Germany

2. Department of Pathology, Kiel Paediatric Cancer Registry; Christian Albrechts University; Kiel Germany

3. Institute for Pathology; Wuerzburg University; Wuerzburg Germany

4. Department of Pediatric Oncology and Hematology; Saarland University Hospital; Homburg Germany

5. Comprehensive Cancer Center Mainfranken; Wuerzburg University; Wuerzburg Germany

Funder

Deutsche Forschungsgemeinschaft

Deutsche Krebshilfe

Publisher

Wiley

Subject

Pathology and Forensic Medicine

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4. Survival in nephroblastoma treated according to the trial and study SIOP-9/GPOH with respect to relapse and morbidity;Weirich;Ann Oncol,2004

5. Results of the SIOP 93-01/GPOH trial and study for the treatment of patients with unilateral nonmetastatic Wilms tumor;Reinhard;Klin Padiatr,2004

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