PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 30296463-0 2018 Bacopa monnieri alleviates paraquat induced toxicity in Drosophila by inhibiting jnk mediated apoptosis through improved mitochondrial function and redox stabilization. Paraquat 27-35 basket Drosophila melanogaster 81-84 35204105-7 2022 Calycosin-fed PQ-exposed flies exhibit significant resistance against PQ-induced mortality and locomotor deficits in terms of reduced oxidative stress, loss of DA neurons, the depletion of dopamine content, and phosphorylated JNK-caspase-3 levels. Paraquat 14-16 basket Drosophila melanogaster 226-229 31481676-6 2019 We found that PQ exposure leads to the activation of the NF-kappaB transcription factor, Relish, and the stress signaling factor JNK, encoded by the gene basket in Drosophila. Paraquat 14-16 basket Drosophila melanogaster 129-132 18538428-6 2008 Moreover, Drosophila fed with (1-200 microM) SP600125, a specific inhibitor of the stress responsive Jun-N-terminal kinase (JNK) signaling, and 20 mM PQ increased survival percentage and movement function (i.e., climbing capability) when compared to flies only treated with PQ. Paraquat 150-152 basket Drosophila melanogaster 101-122 24819147-5 2014 Exposed mth(1) flies exhibit significant resistance against PQ-induced Parkinson"s phenotypes and behavior in terms of oxidative stress, dopaminergic neuronal degeneration, locomotor performance, dopamine content, phosphorylated JNK, pFOXO, Hid, and cleaved caspase-3 levels. Paraquat 60-62 basket Drosophila melanogaster 229-232 24819147-7 2014 The study suggests that lesser activation of JNK-mediated apoptosis in dopaminergic neurons of exposed mth(1) flies protects the organism from PQ-induced damage, which may be causally linked to a common mechanism for PQ-induced neurodegeneration. Paraquat 143-145 basket Drosophila melanogaster 45-48 24819147-7 2014 The study suggests that lesser activation of JNK-mediated apoptosis in dopaminergic neurons of exposed mth(1) flies protects the organism from PQ-induced damage, which may be causally linked to a common mechanism for PQ-induced neurodegeneration. Paraquat 217-219 basket Drosophila melanogaster 45-48 25474322-7 2014 By genetic manipulations, we demonstrate that dMRP4 is required for JNK (c-Jun NH2-terminal kinase) activation during paraquat challenge and for basal transcription of some JNK target genes under normal condition. Paraquat 118-126 basket Drosophila melanogaster 68-71 25474322-7 2014 By genetic manipulations, we demonstrate that dMRP4 is required for JNK (c-Jun NH2-terminal kinase) activation during paraquat challenge and for basal transcription of some JNK target genes under normal condition. Paraquat 118-126 basket Drosophila melanogaster 73-98 24887138-0 2014 Heat shock protein-70 (Hsp-70) suppresses paraquat-induced neurodegeneration by inhibiting JNK and caspase-3 activation in Drosophila model of Parkinson"s disease. Paraquat 42-50 basket Drosophila melanogaster 91-94 19720829-6 2009 Neuronal expression of Jafrac1 also significantly reduced ROS levels, restored mitochondrial function, and attenuated JNK activation caused by paraquat. Paraquat 143-151 basket Drosophila melanogaster 118-121 18538428-6 2008 Moreover, Drosophila fed with (1-200 microM) SP600125, a specific inhibitor of the stress responsive Jun-N-terminal kinase (JNK) signaling, and 20 mM PQ increased survival percentage and movement function (i.e., climbing capability) when compared to flies only treated with PQ. Paraquat 150-152 basket Drosophila melanogaster 124-127