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Menin Interacts with IQGAP1 to Enhance Intercellular Adhesion of β Cells
Multiple endocrine neoplasia type 1 (MEN1) is a dominantly inherited tumor syndrome that results from the mutation of the MEN1 gene that encodes protein menin. Stable overexpression of MEN1 has been shown to partially suppress the RAS-mediated morphological changes of NH3 fibroblast cells. Little is...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2645484/ https://ncbi.nlm.nih.gov/pubmed/19079338 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/onc.2008.435 |
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