PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 23955302-6 2013 These data identify a role for the TSC in responding to ROS at the peroxisome, and identify the peroxisome as a signalling organelle involved in regulation of mTORC1. Reactive Oxygen Species 56-59 TSC complex subunit 1 Homo sapiens 35-38 33860865-5 2021 The study also reveals that treatment of TSC mutant cells with the drug candidate Proxison combined with reduced concentration of rapamycin can increase production of reactive oxygen species (ROS), can modify miRNA expression pattern associated with p53 regulation and can reduce cell viability. Reactive Oxygen Species 167-190 TSC complex subunit 1 Homo sapiens 41-44 33860865-5 2021 The study also reveals that treatment of TSC mutant cells with the drug candidate Proxison combined with reduced concentration of rapamycin can increase production of reactive oxygen species (ROS), can modify miRNA expression pattern associated with p53 regulation and can reduce cell viability. Reactive Oxygen Species 192-195 TSC complex subunit 1 Homo sapiens 41-44 29484365-8 2018 LicA can activate the ULK1/Atg13 complex which is upstream of autophagy, additionally, LicA also can promote ROS generation, ROS trigger the expression level of TSC1/2 complex, PRAS40, CTMP, PP2A, PDK1 and Rubicon change, these molecules are upstream of autophagy. Reactive Oxygen Species 125-128 TSC complex subunit 1 Homo sapiens 161-167 23955302-2 2013 We report that the tuberous sclerosis complex (TSC) signalling node, TSC1, TSC2 and Rheb, localizes to peroxisomes, where it regulates mTORC1 in response to reactive oxygen species (ROS). Reactive Oxygen Species 157-180 TSC complex subunit 1 Homo sapiens 47-50 23955302-2 2013 We report that the tuberous sclerosis complex (TSC) signalling node, TSC1, TSC2 and Rheb, localizes to peroxisomes, where it regulates mTORC1 in response to reactive oxygen species (ROS). Reactive Oxygen Species 157-180 TSC complex subunit 1 Homo sapiens 69-73 23955302-2 2013 We report that the tuberous sclerosis complex (TSC) signalling node, TSC1, TSC2 and Rheb, localizes to peroxisomes, where it regulates mTORC1 in response to reactive oxygen species (ROS). Reactive Oxygen Species 182-185 TSC complex subunit 1 Homo sapiens 47-50 23955302-2 2013 We report that the tuberous sclerosis complex (TSC) signalling node, TSC1, TSC2 and Rheb, localizes to peroxisomes, where it regulates mTORC1 in response to reactive oxygen species (ROS). Reactive Oxygen Species 182-185 TSC complex subunit 1 Homo sapiens 69-73 29522719-5 2018 We further showed that conditional knockout of Tsc1 led to enhanced proliferation and increased reactive oxygen species (ROS) production and phagocytosis in AMs. Reactive Oxygen Species 96-119 TSC complex subunit 1 Homo sapiens 47-51 29522719-5 2018 We further showed that conditional knockout of Tsc1 led to enhanced proliferation and increased reactive oxygen species (ROS) production and phagocytosis in AMs. Reactive Oxygen Species 121-124 TSC complex subunit 1 Homo sapiens 47-51 23257465-4 2012 Many signaling molecules such as FoxOs, ATM, mTOR, TSC1, Bmi1 and AKT play a significant role in ROS-induced HSC senescence. Reactive Oxygen Species 97-100 TSC complex subunit 1 Homo sapiens 51-55 22362037-5 2012 Furthermore, TSC1 is critical for mast cell survival through multiple pathways of apoptosis including the down-regulation of p53, miR-34a, reactive oxygen species, and the up-regulation of Bcl-2. Reactive Oxygen Species 139-162 TSC complex subunit 1 Homo sapiens 13-17 18809716-3 2008 We demonstrate that Tsc1 deletion in the HSCs drives them from quiescence into rapid cycling, with increased mitochondrial biogenesis and elevated levels of reactive oxygen species (ROS). Reactive Oxygen Species 157-180 TSC complex subunit 1 Homo sapiens 20-24 18809716-3 2008 We demonstrate that Tsc1 deletion in the HSCs drives them from quiescence into rapid cycling, with increased mitochondrial biogenesis and elevated levels of reactive oxygen species (ROS). Reactive Oxygen Species 182-185 TSC complex subunit 1 Homo sapiens 20-24