Mutational status of VHL gene and its clinical importance in renal clear cell carcinoma-Reference-Cited by-同舟云学术

Mutational status of VHL gene and its clinical importance in renal clear cell carcinoma

Published:2014-07-16 Issue:3 Volume:465 Page:321-330
ISSN:0945-6317
Container-title:Virchows Archiv
language:en
Short-container-title:Virchows Arch

Author:

Alves Mariana Rezende,Carneiro Felipe Cavalcanti,Lavorato-Rocha André Mourão,da Costa Walter Henriques,da Cunha Isabela Werneck,de Cássio Zequi Stênio,Guimaraes Gustavo Cardoso,Soares Fernando Augusto,Carraro Dirce Maria,Rocha Rafael Malagoli

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology,General Medicine,Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00428-014-1629-z.pdf

Reference32 articles.

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2. Kaelin WG Jr (2002) Molecular basis of the VHL hereditary cancer syndrome. Nat Rev Cancer 2(9):673–682. doi: 10.1038/nrc885

3. Latif F, Tory K, Gnarra J et al (1993) Identification of the von Hippel-Lindau disease tumor suppressor gene. Science 260(5112):1317–1320

4. Kamura T, Koepp DM, Conrad MN et al (1999) Rbx1, a component of the VHL tumor suppressor complex and SCF ubiquitin ligase. Science 284(5414):657–661

5. Carew JS, Esquivel JA, Espitia CM et al (2012) ELR510444 inhibits tumor growth and angiogenesis by abrogating HIF activity and disrupting microtubules inrenal cell carcinoma. PLoS One 7(1):e31120. doi: 10.1371/journal.pone.0031120

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