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Kesinger, Nicholas G
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Acrolein
Kesinger NG
,
Langsdorf BL
,
Yokochi AF
,
Miranda CL
,
Stevens JF
. 2010.
Formation of a vitamin C conjugate of acrolein and its paraoxonase-mediated conversion into 5,6,7,8-tetrahydroxy-4-oxooctanal.
.
Chem Res Toxicol. 23(4):836-44.
Aryldialkylphosphatase
Kesinger NG
,
Langsdorf BL
,
Yokochi AF
,
Miranda CL
,
Stevens JF
. 2010.
Formation of a vitamin C conjugate of acrolein and its paraoxonase-mediated conversion into 5,6,7,8-tetrahydroxy-4-oxooctanal.
.
Chem Res Toxicol. 23(4):836-44.
Ascorbic Acid
Kesinger NG
,
Stevens JF
. 2009.
Covalent interaction of ascorbic acid with natural products.
.
Phytochemistry. 70(17-18):1930-9.
Kesinger NG
,
Langsdorf BL
,
Yokochi AF
,
Miranda CL
,
Stevens JF
. 2010.
Formation of a vitamin C conjugate of acrolein and its paraoxonase-mediated conversion into 5,6,7,8-tetrahydroxy-4-oxooctanal.
.
Chem Res Toxicol. 23(4):836-44.
Cell Line
Kesinger NG
,
Langsdorf BL
,
Yokochi AF
,
Miranda CL
,
Stevens JF
. 2010.
Formation of a vitamin C conjugate of acrolein and its paraoxonase-mediated conversion into 5,6,7,8-tetrahydroxy-4-oxooctanal.
.
Chem Res Toxicol. 23(4):836-44.
Chromatography, High Pressure Liquid
Kesinger NG
,
Langsdorf BL
,
Yokochi AF
,
Miranda CL
,
Stevens JF
. 2010.
Formation of a vitamin C conjugate of acrolein and its paraoxonase-mediated conversion into 5,6,7,8-tetrahydroxy-4-oxooctanal.
.
Chem Res Toxicol. 23(4):836-44.
Eukaryota
Kesinger NG
,
Stevens JF
. 2009.
Covalent interaction of ascorbic acid with natural products.
.
Phytochemistry. 70(17-18):1930-9.
Flavonoids
Kesinger NG
,
Stevens JF
. 2009.
Covalent interaction of ascorbic acid with natural products.
.
Phytochemistry. 70(17-18):1930-9.
Humans
Kesinger NG
,
Langsdorf BL
,
Yokochi AF
,
Miranda CL
,
Stevens JF
. 2010.
Formation of a vitamin C conjugate of acrolein and its paraoxonase-mediated conversion into 5,6,7,8-tetrahydroxy-4-oxooctanal.
.
Chem Res Toxicol. 23(4):836-44.
Isotope Labeling
Kesinger NG
,
Langsdorf BL
,
Yokochi AF
,
Miranda CL
,
Stevens JF
. 2010.
Formation of a vitamin C conjugate of acrolein and its paraoxonase-mediated conversion into 5,6,7,8-tetrahydroxy-4-oxooctanal.
.
Chem Res Toxicol. 23(4):836-44.
Molecular Structure
Kesinger NG
,
Stevens JF
. 2009.
Covalent interaction of ascorbic acid with natural products.
.
Phytochemistry. 70(17-18):1930-9.
Monosaccharides
Kesinger NG
,
Langsdorf BL
,
Yokochi AF
,
Miranda CL
,
Stevens JF
. 2010.
Formation of a vitamin C conjugate of acrolein and its paraoxonase-mediated conversion into 5,6,7,8-tetrahydroxy-4-oxooctanal.
.
Chem Res Toxicol. 23(4):836-44.
Phenols
Kesinger NG
,
Stevens JF
. 2009.
Covalent interaction of ascorbic acid with natural products.
.
Phytochemistry. 70(17-18):1930-9.
Plant Extracts
Kesinger NG
,
Stevens JF
. 2009.
Covalent interaction of ascorbic acid with natural products.
.
Phytochemistry. 70(17-18):1930-9.
Polyphenols
Kesinger NG
,
Stevens JF
. 2009.
Covalent interaction of ascorbic acid with natural products.
.
Phytochemistry. 70(17-18):1930-9.
Recombinant Proteins
Kesinger NG
,
Langsdorf BL
,
Yokochi AF
,
Miranda CL
,
Stevens JF
. 2010.
Formation of a vitamin C conjugate of acrolein and its paraoxonase-mediated conversion into 5,6,7,8-tetrahydroxy-4-oxooctanal.
.
Chem Res Toxicol. 23(4):836-44.
Spectrometry, Mass, Electrospray Ionization
Kesinger NG
,
Langsdorf BL
,
Yokochi AF
,
Miranda CL
,
Stevens JF
. 2010.
Formation of a vitamin C conjugate of acrolein and its paraoxonase-mediated conversion into 5,6,7,8-tetrahydroxy-4-oxooctanal.
.
Chem Res Toxicol. 23(4):836-44.
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