Rand A.A., Rajamani A., Kodani S.D., Harris T.R., Schlatt L., Barnych B., Passerini A.G. and Hammock B.D. Epoxyeicosatrienoic acid (EET)-stimulated angiogenesis is mediated by epoxy hydroxyeicosatrienoic acids (EHETs) formed from COX-2. Journal of Lipid Research. 2019. pp.jlr-M094219.
Harris T.R., Kodani S., Rand A.A., Yang J., Imai D.M., Hwang S-H., Hammock B.D. Celecoxib does not protect against fibrosis and inflammation in a carbon tetrachloride-induced model of liver injury. Molecular Pharmacology. 2018, mol-118.
Bever C., Rand A.A., Nording M., Taft D., Kalanetra K.M., Mills D.A., Breck M.A., Smilowitz J.T., German B., Hammock B.D. Effects of triclosan in breast milk on the infant fecal microbiome. Chemosphere. 2018, 203, 467-473
Rand A.A., Helmer P.O., Inceoglu B., Hammock B.D., Morisseau C. LC-MS/MS analysis of the epoxides and diols derived from the endocannabinoid arachidonoyl ethanolamide. Clinical Metabolomics. Humana Press, New York, NY, 2018. 123-133.
Vasylieva N., Barnych B., Rand A.A., Inceoglu B., Gee S., Hammock B.D. Sensitive immunoassay for detection and quantification of the neurotoxin, tetramethylenedisulfotetramine (TETS). Analytical Chemistry. 2017, 89, 5612-5619
Goswami S.K., Rand A.A., Wan D, Yang J, Inceoglu B, Thomas M, Morisseau C, Yang G-Y, Hammock B. D. Pharmacological inhibition of soluble epoxide hydrolase or genetic deletion reduces diclofenac-induced gastric ulcers. Life Sciences. 2017, 180, 114-122
Rand A.A., Barnych B., Morisseau C., Cajka T., Lee K.S.S., Hammock B.D. Cyclooxygenase derived proangiogenic metabolites of epoxyeicosatrienoic acids. Proceedings of the National Academy of Sciences. 2017, 114, 4370-4375
Barnych B., Rand A.A., Cajka T., Lee K.S.S., Hammock B.D. Synthesis of cyclooxygenase metabolites of 8,9-epoxyeicosatrienoic acid (EETs): 11- and 15-hydroxy 8,9-EETs. Organic and Biomolecular Chemistry. 2017, 15, 4308-4313
Rand A.A., Mabury S.A. Is there a human health risk associated with indirect exposure to perfluorinated carboxylates (PFCAs)? Toxicology. 2017, 375, 28-36
Hwang V.J., Kim J., Rand A.A., Yang C., Sturdivant S., Hammock B., Bell P.D., Guay-Woodford L., Weiss R.H. The cpk model of recessive PKD shows glutamine-dependence associated with the production of the oncometabolite 2-hydroxyglutarate. American Journal of Physiology – Renal Physiology. 2015, 309, F492-F498
Rand A.A., Mabury S.A. Protein binding associated with exposure to fluorotelomer alcohols (FTOHs) and polyfluoroalkyl phosphate esters (PAPs) in rats. Environmental Science and Technology. 2014, 48, 2421-2429
Rand A.A., Rooney J.P., Butt C.M., Meyer J.N., Mabury S.A. Cellular toxicity associated with exposure to perfluorinated carboxylates (PFCAs) and their metabolic precursors. Chemical Research in Toxicology. 2013, 27, 24-50
Rand A.A., Mabury S.A. Covalent binding of fluorotelomer unsaturated aldehydes (FTUALs) and carboxylic acids (FTUCAs) to proteins. Environmental Science and Technology. 2013, 47, 1655–1663
Rand A.A., Mabury S.A. In vitro interactions of biological nucleophiles with fluorotelomer unsaturated acids and aldehydes: fate and consequences. Environmental Science and Technology. 2012, 46, 4398-7406
Rand A.A., Mabury S.A. Assessing the structure–activity relationships of fluorotelomer unsaturated acids and aldehydes with glutathione. Cell Biology and Toxicology. 2012, 28, 115–124
Rand A.A., Mabury, S.A. Perfluorinated carboxylic acids in directly fluorinated high density polyethylene material. Environmental Science and Technology. 2011, 45, 8053-8059.
Rand A.A., Barclay L.R.C. Photo-oxidations initiated by UV radiation of urocanic acid and its methyl ester in solution, micelles, and lipid bilayers: TYPE I (free radical) or TYPE II (singlet oxygen) mechanisms depend on the medium. Journal of Photochemistry and Photobiology A. 2009, 208, 79-90
Chepelev L.L., Beshara C.S., MacLean P.D., Hatfield G.L., Rand A.A., Thompson A., Wright J.S., Barclay L.R.C. Polypyrroles as antioxidants: kinetic studies on reactions of bilirubin and biliverdin dimethyl esters and synthetic model compounds with peroxyl radicals in solution. Chemical calculations on selected typical structures. Journal of Organic Chemistry. 2006, 71(1), 22-30