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TSC1/TSC2 Signaling in the CNS
Over the past several years, the study of a hereditary tumor syndrome, tuberous sclerosis complex (TSC), has shed light on the regulation of cellular proliferation and growth. TSC is an autosomal dominant disorder that is due to inactivating mutations in TSC1 or TSC2 and characterized by benign tumo...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
2011
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| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3070766/ https://ncbi.nlm.nih.gov/pubmed/21329690 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.febslet.2011.02.001 |
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