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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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Bibliografske podrobnosti
Main Authors: Han, Juliette M., Sahin, Mustafa
Format: Artigo
Jezik:Inglês
Izdano: 2011
Teme:
Online dostop: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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