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Control of mTORC1 signaling by the Opitz syndrome protein MID1
Mutations in the MID1 gene are causally linked to X-linked Opitz BBB/G syndrome (OS), a congenital disorder that primarily affects the formation of diverse ventral midline structures. The MID1 protein has been shown to function as an E3 ligase targeting the catalytic subunit of protein phosphatase 2...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3102420/ https://ncbi.nlm.nih.gov/pubmed/21555591 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1100131108 |
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