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In Search of Tumor Suppressing Functions of Menin
Human hereditary tumor syndromes serve as an ideal model for studying molecular pathways regulating tumorigenesis. Multiple endocrine neoplasia type 1 (MEN1), a human familial tumor syndrome, results from mutations in the Men1 gene. Men1 encodes a novel tumor suppressor, menin, of unknown biochemica...
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| Main Authors: | , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2007
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1919399/ https://ncbi.nlm.nih.gov/pubmed/17222504 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mce.2006.12.032 |
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