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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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| Autores principales: | , , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2003
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| Materias: | |
| Acceso en línea: | 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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