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Chandra Dodia

Researcher at University of Pennsylvania

Publications -  81
Citations -  3890

Chandra Dodia is an academic researcher from University of Pennsylvania. The author has contributed to research in topics: Phospholipase A2 & Phospholipid. The author has an hindex of 35, co-authored 80 publications receiving 3635 citations. Previous affiliations of Chandra Dodia include University of Delaware.

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Journal ArticleDOI

1-Cys peroxiredoxin, a bifunctional enzyme with glutathione peroxidase and phospholipase A2 activities.

TL;DR: The results suggest that Ser32 in the GDSWG consensus sequence provides the catalytic nucleophile for the hydrolase activity of aiPLA2, while Cys47 in the PVCTTE consensus sequence is at the active site for peroxidase activity.
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Phospholipid hydroperoxides are substrates for non-selenium glutathione peroxidase.

TL;DR: This study investigated phospholipid hydroperoxides as substrates for non-selenium GSH peroxidase (NSGPx), an enzyme also called 1-Cys peroxiredoxin, which is an important component of cellular antioxidant defense systems.
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Endothelial NADPH Oxidase as the Source of Oxidants in Lungs Exposed to Ischemia or High K

TL;DR: It is demonstrated that ROS production in lungs exposed to ischemia or high K+ results from assembly and activation of a membrane-associated NAPDH oxidase of the pulmonary endothelium, and the increased dichlorofluorescein fluorescence in these models of ROS generation was localized primarily to the pulmonary artery endothelial cells.
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Simulated Ischemia in Flow-Adapted Endothelial Cells Leads to Generation of Reactive Oxygen Species and Cell Signaling

TL;DR: It is concluded that flow-adapted endothelial cells generate ROS with ischemia that results in activation of NF-kappaB and AP-1 and an increase of DNA synthesis and this effect is not mediated by hypoxia, implicating a role for mechanotransduction in ischemIA-mediated cell signaling.
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ABCA3 Is Critical for Lamellar Body Biogenesis in Vivo

TL;DR: It is suggested that ABCA3 is necessary for lamellar body biogenesis, surfactant protein-B processing, and lung development late in gestation, since the fraction of near term Abca3/– embryos was significantly lower than expected from Mendelian inheritance.