|1.||Wang, Qingshan: 2 articles (05/2015 - 12/2014)|
|2.||Chu, Chun-Hsien: 2 articles (05/2015 - 12/2014)|
|3.||Oyarzabal, Esteban: 2 articles (05/2015 - 12/2014)|
|4.||Hong, Jau-Shyong: 2 articles (05/2015 - 12/2014)|
|5.||Chen, Shih-Heng: 2 articles (05/2015 - 12/2014)|
|6.||Qian, Li: 2 articles (05/2015 - 12/2014)|
|7.||Wilson, Belinda: 2 articles (05/2015 - 12/2014)|
|8.||Kim, Seok Hyun: 2 articles (02/2015 - 10/2010)|
|9.||You, Hye Jin: 2 articles (02/2015 - 10/2010)|
|10.||Paek, A Rome: 2 articles (02/2015 - 10/2010)|
|1.||Dehydration (Water Stress)
06/15/2015 - "Diphenyleneiodonium chloride (DPI), a specific inhibitor of NADPH oxidase, was effective in inhibiting the accumulation of hydrogen peroxide as well as of jasmonates upon dehydration. "
12/01/2002 - "Pretreatment with some ROS scavengers, such as Tiron and dimethylthiourea (DMTU), and an inhibitor of NAD(P)H oxidase, diphenyleneiodonium (DPI), almost completely arrested the increase in ROS and the activities of these antioxidant enzymes induced by water stress or ABA treatment. "
|2.||Hypertension (High Blood Pressure)
09/01/2008 - "WST-1/1-methoxy-phenazine methosulphate reduction was unaffected by anoxia and relatively insensitive to diphenyleneiodonium. "
01/01/1999 - "5. Diphenylene iodonium (DPI; 1 microM) suppressed outward K+ current by approximately 42%, and DPI + hypoxia had no additional effect on the K+ current. "
09/01/1997 - "To investigate mechanisms of inhibition of hypoxic pulmonary vasoconstriction (HPV), we studied pulmonary artery smooth muscle cell (PASMC) responses to hypoxia, utilizing diphenyleneiodonium (DPI), which blocks HPV. "
09/01/1997 - "Pulmonary artery smooth muscle cell [Ca2+]i and contraction: responses to diphenyleneiodonium and hypoxia."
11/15/1995 - "In each case, the response to hypoxia was specifically inhibited by low doses of diphenylene iodonium (Ph1I+). "
09/01/2014 - "Furthermore, inhibition of NOX-mediated ROS production with apocynin, diphenylene iodonium (DPI) or NOX2 docking sequence (Nox2ds)-tat peptide during these first 4h of PE stimulation significantly inhibited PE-induced hypertrophy of H9c2 cells, both after 24 and 48h of PE stimulation. "
06/01/2007 - "In this study, we demonstrate that TGF-beta1 is a potent inducer of expression of the nonphagocyte NAD(P)H oxidase catalytic homolog Nox4, diphenylene iodonium-inhibitable reactive oxygen species production, proliferation, and hypertrophy in cultured human airway smooth muscle cells. "
|5.||Colonic Neoplasms (Colon Cancer)
04/01/2013 - "We found that diphenyleneiodonium (DPI), di-2-thienyliodonium (DTI), and iodonium diphenyl inhibited the growth of Caco2, HT-29, and LS-174T colon cancer cells at concentrations (10-250nM for DPI, 0.5-2.5μM for DTI, and 155nM to 10μM for iodonium diphenyl) substantially lower than needed for DU145 human prostate cancer cells, which do not possess functional NADPH oxidase activity. "
10/31/2010 - "In the present study, we observed that IGF-1 was able to induce ZNF143 expression in HCT116 human colon cancer cells and that wortmannin, an inhibitor of phosphatidylinositide 3- kinase (PI3-kinase), inhibited this induction, as did diphenyleneiodonium (DPI), an NADPH oxidase inhibitor, and monodansylcardavarine (MDC), a receptor internalization inhibitor. "
|1.||NADPH Oxidase (NAD(P)H oxidase)
|2.||Hydrogen Peroxide (Hydroperoxide)
|3.||Protein Kinase C
|5.||3- benzyl- 7- (2- benzoxazolyl)thio- 1,2,3- triazolo(4,5- d)pyrimidine
|6.||6,8-diallyl 5,7-dihydroxy 2-(2-allyl 3-hydroxy 4-methoxyphenyl)1-H benzo(b)pyran-4-one
|7.||Reactive Oxygen Species (Oxygen Radicals)