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8. mTORC2 is required for proliferation and survival of TSC2-null cells. Goncharova EA, Goncharov DA, Li H, Pimtong W, Lu S, Khavin I, Krymskaya VP. Mol Cell Biol; 2011 Jun 15; 31(12):2484-98. PubMed ID: 21482669 [Abstract] [Full Text] [Related]
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11. Tsc2 gene inactivation causes a more severe epilepsy phenotype than Tsc1 inactivation in a mouse model of tuberous sclerosis complex. Zeng LH, Rensing NR, Zhang B, Gutmann DH, Gambello MJ, Wong M. Hum Mol Genet; 2011 Feb 01; 20(3):445-54. PubMed ID: 21062901 [Abstract] [Full Text] [Related]
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14. Tumor suppressors TSC1 and TSC2 differentially modulate actin cytoskeleton and motility of mouse embryonic fibroblasts. Goncharova EA, James ML, Kudryashova TV, Goncharov DA, Krymskaya VP. PLoS One; 2014 Nov 05; 9(10):e111476. PubMed ID: 25360538 [Abstract] [Full Text] [Related]
15. Ablation of the mTORC2 component rictor in brain or Purkinje cells affects size and neuron morphology. Thomanetz V, Angliker N, Cloëtta D, Lustenberger RM, Schweighauser M, Oliveri F, Suzuki N, Rüegg MA. J Cell Biol; 2013 Apr 15; 201(2):293-308. PubMed ID: 23569215 [Abstract] [Full Text] [Related]
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19. Complex Neurological Phenotype in Mutant Mice Lacking Tsc2 in Excitatory Neurons of the Developing Forebrain(123). Crowell B, Lee GH, Nikolaeva I, Dal Pozzo V, D'Arcangelo G. eNeuro; 2015 Nov 12; 2(6):. PubMed ID: 26693177 [Abstract] [Full Text] [Related]
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