Ion solvation by channel carbonyls characterized by 17O solid-state NMR at 21 T. Hu J, Chekmenev EY, Gan Z, Gor'kov PL, Saha S, Brey WW, Cross TA (2005) J Am Chem Soc 127: 11922-3 Ion-binding study by 17O solid-state NMR spectroscopy in the model peptide Gly-Gly-Gly at 19.6 T. Chekmenev EY, Waddell KW, Hu J, Gan Z, Wittebort RJ, Cross TA (2006) J Am Chem Soc 128: 9849-55 Isolation and characterization of natural allene oxides: unstable intermediates in the metabolism of lipid hydroperoxides. Brash AR, Baertschi SW, Ingram CD, Harris TM (1988) Proc Natl Acad Sci U S A 85: 3382-6 Voxelwise Relationships Between Distribution Volume Ratio and Cerebral Blood Flow: Implications for Analysis of β-Amyloid Images. Sojkova J, Goh J, Bilgel M, Landman B, Yang X, Zhou Y, An Y, Beason-Held LL, Kraut MA, Wong DF, Resnick SM (2015) J Nucl Med 56: 1042-7 Untargeted analysis of mass spectrometry data for elucidation of metabolites and function of enzymes. Sanchez-Ponce R, Guengerich FP (2007) Anal Chem 79: 3355-62 Reassignment of organic peroxyl radical adducts. Dikalov SI, Mason RP (1999) Free Radic Biol Med 27: 864-72 On non-cyclooxygenase prostaglandin synthesis in the sea whip coral, Plexaura homomalla: an 8(R)-lipoxygenase pathway leads to formation of an alpha-ketol and a Racemic prostanoid. Brash AR, Baertschi SW, Ingram CD, Harris TM (1987) J Biol Chem 262: 15829-39 31P and 13C NMR studies of oxygen transfer during catalysis by 3-deoxy-D-manno-octulosonate cytidylyltransferase from Escherichia coli. Kohlbrenner WE, Nuss MM, Fesik SW (1987) J Biol Chem 262: 4534-7 Unraveling curcumin degradation: autoxidation proceeds through spiroepoxide and vinylether intermediates en route to the main bicyclopentadione. Gordon ON, Luis PB, Sintim HO, Schneider C (2015) J Biol Chem 290: 4817-4828 Dysfunctional role of parietal lobe during self-face recognition in schizophrenia. Yun JY, Hur JW, Jung WH, Jang JH, Youn T, Kang DH, Park S, Kwon JS (2014) Schizophr Res 152: 81-8 Doubly labeled water is a validated and verified reference standard in nutrition research. Buchowski MS (2014) J Nutr 144: 573-4 Cholesterol synthesis and absorption by 2H2O and 18O-cholesterol and hypocholesterolemic effect of soy protein. Wong WW, Hachey DL, Clarke LL, Zhang S (1995) J Nutr 125: 612S-618S Degradation pathway of bisphenol A: does ipso substitution apply to phenols containing a quaternary alpha-carbon structure in the para position? Kolvenbach B, Schlaich N, Raoui Z, Prell J, Zühlke S, Schäffer A, Guengerich FP, Corvini PF (2007) Appl Environ Microbiol 73: 4776-84 Flow-through lipid nanotube arrays for structure-function studies of membrane proteins by solid-state NMR spectroscopy. Chekmenev EY, Gor'kov PL, Cross TA, Alaouie AM, Smirnov AI (2006) Biophys J 91: 3076-84 7-HETE, 10-HETE, and 13-HETE are major products of NADPH-dependent arachidonic acid metabolism in rat liver microsomes: analysis of their stereochemistry, and the stereochemistry of their acid-catalyzed rearrangement. Brash AR, Boeglin WE, Capdevila JH, Yeola S, Blair IA (1995) Arch Biochem Biophys 321: 485-92 The role of aldehyde oxidase and xanthine oxidase in the biotransformation of a novel negative allosteric modulator of metabotropic glutamate receptor subtype 5. Morrison RD, Blobaum AL, Byers FW, Santomango TS, Bridges TM, Stec D, Brewer KA, Sanchez-Ponce R, Corlew MM, Rush R, Felts AS, Manka J, Bates BS, Venable DF, Rodriguez AL, Jones CK, Niswender CM, Conn PJ, Lindsley CW, Emmitte KA, Daniels JS (2012) Drug Metab Dispos 40: 1834-45 Quantification of the major urinary metabolite of 15-F2t-isoprostane (8-iso-PGF2alpha) by a stable isotope dilution mass spectrometric assay. Morrow JD, Zackert WE, Yang JP, Kurhts EH, Callewaert D, Dworski R, Kanai K, Taber D, Moore K, Oates JA, Roberts LJ (1999) Anal Biochem 269: 326-31 Mapping hypoxia-induced bioenergetic rearrangements and metabolic signaling by 18O-assisted 31P NMR and 1H NMR spectroscopy. Pucar D, Dzeja PP, Bast P, Gumina RJ, Drahl C, Lim L, Juranic N, Macura S, Terzic A (2004) Mol Cell Biochem 256-257: 281-9
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