PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 29903185-8 2017 07), the TGF-beta +DPI group is( 0. 3-aminodiphenyleneiodium 19-22 transforming growth factor beta 1 Homo sapiens 9-17 29903185-15 2017 6), the TGF-beta + DPI group is( 1. 3-aminodiphenyleneiodium 19-22 transforming growth factor beta 1 Homo sapiens 8-16 29903185-21 2017 1), the TGF-beta + DPI group is( 3. 3-aminodiphenyleneiodium 19-22 transforming growth factor beta 1 Homo sapiens 8-16 29903185-27 2017 Then TGF-beta + DPI group compared with the TGF-beta group, the scratch healing rate is decreased( F = 33. 3-aminodiphenyleneiodium 16-19 transforming growth factor beta 1 Homo sapiens 5-13 29903185-31 2017 CONCLUSION: After the NOX4 was inhibited by DPI, TGF-beta-induced migration of A549 cells was inhibited. 3-aminodiphenyleneiodium 44-47 transforming growth factor beta 1 Homo sapiens 49-57 25175743-8 2014 Using a NOX inhibitor (DPI) and cells expressing a shRNA for NOX4, we demonstrated that TGF-beta1 promotes an oxidative environment that favors myofibroblastic differentiation. 3-aminodiphenyleneiodium 23-26 transforming growth factor beta 1 Homo sapiens 88-97 20204677-6 2010 Our results shows that TGF-beta1 stimulation of uPA and MMP-9 expression involve NOXs-dependent ROS and NFkappaB, activation, demonstrated by using DPI, NOXs inhibitor, ROS scavenger N-acetylcysteine and SN50, an NFkb inhibitor. 3-aminodiphenyleneiodium 148-151 transforming growth factor beta 1 Homo sapiens 23-32 32736702-5 2020 TGF-beta1 treatment increased reactive oxygen species (ROS) via NOX4 upregulation, which acts downstream of ERK and mTORC1, as the ROS scavenger N-acetylcysteine and a pan-NADPH oxidase (NOX) inhibitor DPI dissipated excess ROS generation. 3-aminodiphenyleneiodium 202-205 transforming growth factor beta 1 Homo sapiens 0-9 16159901-6 2005 TGF-beta stimulation of ROS was mediated by the NAPDH oxidase homolog Nox4 as DPI, an inhibitor of NADPH oxidase, and dominant-negative Nox4 adenovirus blocked ROS production. 3-aminodiphenyleneiodium 78-81 transforming growth factor beta 1 Homo sapiens 0-8 11494050-5 2001 We also observed that TGF-beta-induced p38 activation was inhibited by PDTC, pyrrolidinedithiocarbamate, a known antioxidant, and DPI, diphenylene iodonium chloride, one of the known NADPH oxidase inhibitors. 3-aminodiphenyleneiodium 130-133 transforming growth factor beta 1 Homo sapiens 22-30 11494050-9 2001 DPI, an inhibitor of NADPH oxidase, inhibited TGF-beta-induced ROS production. 3-aminodiphenyleneiodium 0-3 transforming growth factor beta 1 Homo sapiens 46-54 11494050-12 2001 Pretreatment with DPI dramatically reduced TGF-beta-induced NADPH oxidase activity. 3-aminodiphenyleneiodium 18-21 transforming growth factor beta 1 Homo sapiens 43-51 32736702-6 2020 TGF-beta1-induced oxidative stress resulted in EMT and fibrotic changes, as NAC and DPI prevented alpha-SMA, Col4alpha3 expression and cell migration. 3-aminodiphenyleneiodium 84-87 transforming growth factor beta 1 Homo sapiens 0-9