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Menin induces endodermal differentiation in aggregated P19 stem cells by modulating the retinoic acid receptors
Menin, a ubiquitously expressed protein, is the product of the multiple endocrine neoplasia type I (Men1) gene, mutations of which cause tumors primarily of the parathyroid, endocrine pancreas, and anterior pituitary. Menin-null mice display early embryonic lethality, and thus imply a critical role...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3412628/ https://ncbi.nlm.nih.gov/pubmed/21833538 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11010-011-1003-2 |
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