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Published in 2017 at "Oncotarget"
DOI: 10.18632/oncotarget.18963
Abstract: Hyperactivation of mammalian target of rapamycin complex 1 (mTORC1), caused by loss-of-function mutations in either the TSC1 or TSC2 gene, leads to the development of tuberous sclerosis complex (TSC), a benign tumor syndrome with multiple…
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Keywords:
akt;
tuberous sclerosis;
sclerosis complex;
foxo3a pdgfr ... See more keywords