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Molecular Pathogenesis of Pancreatic Neuroendocrine Tumors

Pancreatic neuroendocrine tumors (PNETs) are rare primary neoplasms of the pancreas and arise sporadically or in the context of genetically determined syndromes. Depending on hormone production and sensing, PNETs clinically manifest due to a hormone-related syndrome (functional PNET) or by symptoms...

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Bibliografske podrobnosti
Main Authors: Ehehalt, Florian, Franke, Ellen, Pilarsky, Christian, Grützmann, Robert
Format: Artigo
Jezik:Inglês
Izdano: MDPI 2010
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC3840460/
https://ncbi.nlm.nih.gov/pubmed/24281208
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cancers2041901
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