Two well-differentiated pancreatic neuroendocrine tumor mouse models

Multiple endocrine neoplasia type 1 (MEN1) is a genetic syndrome in which patients develop neuroendocrine tumors (NETs), including pancreatic neuroendocrine tumors (PanNETs). The prolonged latency of tumor development in MEN1 patients suggests a likelihood that other mutations cooperate with Men1 to...

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Publicat a:Cell Death Differ
Autors principals: Wong, Chung, Tang, Laura H., Davidson, Christian, Vosburgh, Evan, Chen, Wenjin, Foran, David J., Notterman, Daniel A., Levine, Arnold J., Xu, Eugenia Y.
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group UK 2019
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7206057/
https://ncbi.nlm.nih.gov/pubmed/31160716
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41418-019-0355-0
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