Chromosome 17p13 deletion is associated with an aggressive tumor phenotype in clear cell renal cell carcinoma

BACKGROUND: Deletions of 17p13 recurrently occur in renal cell carcinoma (RCC) but their prognostic role seems to be uncertain. METHODS: To determine prevalence, relationship with tumor phenotype, and patient prognosis, a tissue microarray containing samples from 1809 RCCs was evaluated using dual l...

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Detalles Bibliográficos
Autores principales: Eichenauer, Till, Shadanpour, Navid, Kluth, Martina, Göbel, Cosima, Weidemann, Sören, Fraune, Christoph, Büscheck, Franziska, Hube-Magg, Claudia, Möller-Koop, Christina, Dahlem, Roland, Fisch, Margit, Rink, Michael, Riechardt, Silke, Burandt, Eike, Bernreuther, Christian, Minner, Sarah, Simon, Ronald, Sauter, Guido, Wilczak, Waldemar, Clauditz, Till
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293794/
https://www.ncbi.nlm.nih.gov/pubmed/32534597
http://dx.doi.org/10.1186/s12957-020-01902-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293794/
https://www.ncbi.nlm.nih.gov/pubmed/32534597
http://dx.doi.org/10.1186/s12957-020-01902-y

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