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Translational Diagnostics and Therapeutics in Pancreatic Neuroendocrine Tumors

Pancreatic neuroendocrine tumors (PNETs) are rare tumors, but have been increasing in incidence. Although typically thought of as indolent, more than half of patients present with metastatic disease. For many years, the only mutations commonly known in these tumors were those in the MEN1 gene. Recen...

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Dettagli Bibliografici
Pubblicato in:Clin Cancer Res
Autori principali: Maxwell, Jessica E., Sherman, Scott K., Howe, James R.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2016
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5082425/
https://ncbi.nlm.nih.gov/pubmed/27742788
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1158/1078-0432.CCR-16-0435
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