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- Data for: Role of astrocytes-derived D-serine in PFOS-induced neurotoxicity through NMDARs in the rat primary hippocampal neuronsThe uoload data included the data in MTT, APOPTOSIS, GENE, PROTEIN, CALCIUM and D-serine.
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- (Toxicology) Identifying Environmental Chemicals as Agonists of the Androgen Receptor by Applying a Quantitative High-throughput Screening PlatformThe paper has data generated by NIH and the EPA coauthors provided input into the preparation of the manuscript
- Dataset
- Crystal structure of sarin surrogate NIMP inhibited recombinant human bile salt activated lipase
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- Crystal structure of ethyl-paraoxon inhibited recombinant human bile salt activated lipase (aged form)
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- Crystal structure of VX surrogate NEMP inhibited recombinant human bile salt activated lipase
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- Crystal structure of native recombinant human bile salt activated lipase
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- Crystal structure of tabun surrogate NEDPA inhibited recombinant human bile salt activated lipase
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- H20 disinfection_Science Hub_2022Dataset used to generate tables/figures demonstrating the effects of water disinfection on allergic hypersensitivity and dermal irritation.
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- The Dynamicity of Acute Ozone-Induced Systemic Leukocyte Trafficking and Adrenal-Derived Stress HormonesOzone exposure induces neuroendocrine stress response, which causes lymphopenia. We hypothesized that ozone-induced increases in stress hormones will temporally follow changes in circulating granulocytes, monocytes and lymphocyte subpopulations. The goal of this study was to chronicle the changes in circulating stress hormones, cytokines, and leukocyte trafficking during 4-hour exposure to ozone. Male Wistar Kyoto rats were exposed to air or ozone (0.4 or 0.8 ppm) for 0.5, 1, 2, or 4 hours. After each time point, we assessed, circulating stress hormones and cytokines, lung gene expression, and live and apoptotic granulocytes, monocytes (classical and non-classical), and lymphocytes (B, Th and Tc) in blood, thymus and spleen using flow cytometry.
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- PFESABP2v01Data for individual animals used to create the information demonstrated in Table 1 of the manuscript, including PFESA BP2 serum and liver concentrations and serum clinical chemistry values
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