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Direct Binding of DNA by Tumor Suppressor Menin
Menin is a tumor suppressor that is mutated in patients with multiple endocrine neoplasia type I (MEN1), an inherited tumor-prone syndrome. Since there is no obvious conserved structural domain in menin that suggests a function, little is known as to how menin suppresses tumorigenisis. Although meni...
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| Autori principali: | , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2004
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2858586/ https://ncbi.nlm.nih.gov/pubmed/15331604 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M409358200 |
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