Genetic Deletion of Menin in Mouse Mesenchymal Stem Cells: An Experimental and Computational Analysis
ABSTRACT Loss‐of‐function mutations in the MEN1 tumor‐suppressor gene cause the multiple endocrine neoplasia type 1 syndrome. Menin, the MEN1 gene product, is expressed in many tissues, including bone, where its function remains elusive. We conditionally inactivated menin in mesenchymal stem cells (...
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| Principais autores: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Oxford University Press
2022-05-01
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| Series: | JBMR Plus |
| Assuntos: | |
| Acceso en liña: | https://doi.org/10.1002/jbm4.10622 |
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