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Altered PTEN, ATRX, CHGA, CHGB, and TP53 Expression Are Associated with Aggressive VHL-Associated Pancreatic Neuroendocrine Tumors

Von Hippel-Lindau (VHL) syndrome is an inherited cancer syndrome in which 8–17 % of germline mutation carriers develop pancreatic neuroendocrine tumors (PNETs). There is limited data on prognostic markers for PNETs other than Ki-67, which is included in the World Health Organization classification s...

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Detalhes bibliográficos
Main Authors: Weisbrod, Allison B., Zhang, Lisa, Jain, Meenu, Barak, Stephanie, Quezado, Martha M., Kebebew, Electron
Formato: Artigo
Idioma:Inglês
Publicado em: Springer-Verlag 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3644020/
https://ncbi.nlm.nih.gov/pubmed/23361940
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12672-013-0134-1
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