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Menin Induces Apoptosis in Murine Embryonic Fibroblasts

Multiple endocrine neoplasia type I (MEN1) is a hereditary tumor syndrome characterized by multiple endocrine and occasionally non-endocrine tumors. The tumor suppressor gene Men1, which is frequently mutated in MEN1 patients, encodes the nuclear protein menin. Although many tumor suppressor genes a...

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Autors principals: Schnepp, Robert W., Mao, Hua, Sykes, Stephen M., Zong, Wei-Xing, Silva, Albert, La, Ping, Hua, Xianxin
Format: Artigo
Idioma:Inglês
Publicat: 2003
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2858560/
https://ncbi.nlm.nih.gov/pubmed/14688275
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M308073200
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