Genomic imbalances pinpoint potential oncogenes and tumor suppressors in Wilms tumors-Reference-Cited by-同舟云学术

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Genomic imbalances pinpoint potential oncogenes and tumor suppressors in Wilms tumors

Published:2016-02-24 Issue:1 Volume:9 Page:
ISSN:1755-8166
Container-title:Molecular Cytogenetics
language:en
Short-container-title:Mol Cytogenet

Author:

Krepischi A. C. V.,Maschietto M.,Ferreira E. N.,Silva A. G.,Costa S. S.,da Cunha I. W.,Barros B. D. F.,Grundy P. E.,Rosenberg C.,Carraro D. M.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Fundação de Amparo à Pesquisa do Estado de São Paulo (BR)

Fundação de Amparo à Pesquisa do Estado de São Paulo

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry, medical,Genetics(clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Link

http://link.springer.com/content/pdf/10.1186/s13039-016-0227-y

Reference47 articles.

1. Stiller CA, Parkin DM. International variations in the incidence of childhood renal tumours. Br J Cancer. 1990;62:1026–30.

2. Wilms’ tumor: status report, 1990. By the National Wilms’ Tumor Study Committee. J Clin Oncol. 1991;9:877–87

3. Mierau GW, Beckwith JB, Weeks DA. Ultrastructure and histogenesis of the renal tumors of childhood: an overview. Ultrastruct Pathol. 1987;11:313–33.

4. Beckwith JB. Histopathological aspects of renal tumors in children. Prog Clin Biol Res. 1982;100:1–14.

5. Maschietto M, De Camargo B, Brentani H, Grundy P, Sredni ST, Torres C, Mota LD, Cunha IW, Patrão DFC, Costa CML, Soares FA, Brentani RR, Carraro DM. Molecular profiling of isolated histological components of Wilms tumor implicates a common role for the Wnt signaling pathway in kidney and tumor development. Oncology. 2008;75:81–91.

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