Pancreatic Neuroendocrine Tumors: Molecular Mechanisms and Therapeutic Targets

SIMPLE SUMMARY: Pancreatic neuroendocrine tumors (pNETs) are rare, indolent cancers whose causation is only partly understood. An increasing number of studies have uncovered molecular changes associated with pNETs, helping to identify common disease mechanisms. This knowledge has guided current pNET...

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Detalles Bibliográficos
Autores principales: Maharjan, Chandra K., Ear, Po Hien, Tran, Catherine G., Howe, James R., Chandrasekharan, Chandrikha, Quelle, Dawn E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533967/
https://www.ncbi.nlm.nih.gov/pubmed/34680266
http://dx.doi.org/10.3390/cancers13205117

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533967/
https://www.ncbi.nlm.nih.gov/pubmed/34680266
http://dx.doi.org/10.3390/cancers13205117

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