Search Results - "Yurawecz, Martin P"

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    Mammary lipogenic enzyme activity, trans fatty acids and conjugated linoleic acids are altered in lactating dairy cows fed a milk fat-depressing diet by Piperova, L S, Teter, B B, Bruckental, I, Sampugna, J, Mills, S E, Yurawecz, M P, Fritsche, J, Ku, K, Erdman, R A

    Published in The Journal of nutrition (01-10-2000)
    “…The objectives of the present study were to examine the effect of a milk fat-depressing (MFD) diet on: 1) the activity of mammary acetyl-CoA carboxylase (ACC)…”
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    Identification and Characterization of Conjugated Fatty Acid Methyl Esters of Mixed Double Bond Geometry by Acetonitrile Chemical Ionization Tandem Mass Spectrometry by Michaud, Anthony L, Yurawecz, Martin P, Delmonte, Pierluigi, Corl, Benjamin A, Bauman, Dale E, Brenna, J. Thomas

    Published in Analytical chemistry (Washington) (15-09-2003)
    “…Fatty acids with conjugated double bonds have attracted great interest because of their reported potent bioactivities. However, there are currently no rapid…”
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    Silver-ion high-performance liquid chromatographic separation and identification of conjugated linoleic acid isomers by Sehat, N, Yurawecz, M.P, Roach, J.A.G, Mossoba, M.M, Kramer, J.K.G, Ku, Y

    Published in Lipids (01-02-1998)
    “…This is the first report of the application of silverion impregnated high‐performance liquid chromatography (Ag+‐HPLC) to the separation of complex mixtures of…”
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    Distributions of conjugated linoleic acid (CLA) isomers in tissue lipid classes of pigs fed a commercial CLA mixture determined by gas chromatography and silver ion-high-performance liquid chromatography by Kramer, J.K.C, Sehat, N, Dugan, M.E.R, Mossoba, M.M, Yurawecz, M.P, Roach, J.A.G, Eulitz, K, Aalhus, J.L, Schafer, A.L, Ku, Y

    Published in Lipids (01-06-1998)
    “…Pigs were fed a commercial conjugated linoleic acid (CLA) mixture, prepared by alkali isomerization of sunflower oil, at 2% of the basal diet, from 61.5 to 106…”
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    Trans, saturated, and unsaturated fat in foods in the United States prior to mandatory trans-fat labeling by Satchithanandam, S, Oles, C.J, Spease, C.J, Brandt, M.M, Yurawecz, M.P, Rader, J.I

    Published in Lipids (2004)
    “…On July 11, 2003, the U.S. Food and Drug Administration published a final rule amending its food‐labeling regulations to require that trans FA be declared in…”
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    Improved separation of conjugated fatty acid methyl esters by silver ion-high-performance liquid chromatography by Sehat, N, Rickert, R, Mossoba, M.M, Kramer, J.K.G, Yurawecz, M.P, Roach, J.A.G, Adlof, R.O, Morehouse, K.M, Fritsche, J, Eulitz, K.D

    Published in Lipids (01-04-1999)
    “…Operating from one to six silver ion‐high‐performance liquid chromatography (Ag+‐HPLC) columns in series progressively improved the resolution of the methyl…”
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    A new conjugated linoleic acid isomer, 7 trans, 9 cis-octadecadienoic acid, in cow milk, cheese, beef and human milk and adipose tissue by Yurawecz, M.P. (U.S. Food and Drug Administration, Washington, DC.), Roach, J.A.G, Sehat, N, Mossoba, M.M, Kramer, J.K.G, Fritsche, J, Steinhart, H, Ku, Y

    Published in Lipids (01-08-1998)
    “…The identity of a previously unrecognized conjugated linoleic acid (CLA) isomer, 7 trans, 9 cis‐octadecadienoic acid (18∶2) was confirmed in milk, cheese,…”
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    Overview of infrared methodologies for trans fat determination by Mossoba, M.M, Yurawecz, M.P, Delmonte, P, Kramer, J.K.G

    Published in Journal of AOAC International (01-03-2004)
    “…trans Fatty acids are present in a variety of foods like dairy products, but the major sources are products that contain commercially hydrogenated fats. Some…”
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    Improved identification of conjugated linoleic acid isomers using silver-ion HPLC separations by Delmonte, P, Yurawecz, M.P, Mossoba, M.M, Cruz-Hernandez, C, Kramer, J.K.G

    Published in Journal of AOAC International (01-03-2004)
    “…Silver-ion high-performance liquid chromatography (Ag(+)-HPLC) has been shown to be effective in the resolution of most of the isomers of conjugated…”
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    Lipase-catalyzed fractionation of conjugated linoleic acid isomers by Haas, M.J, Kramer, J.K.G, McNeill, G, Scott, K, Foglia, T.A, Sehat, N, Fritsche, J, Mossoba, M.M, Yurawecz, M.P

    Published in Lipids (01-09-1999)
    “…The abilities of lipases produced by the fungus Geotrichum candidum to selectively fractionate mixtures of conjugated linoleic acid (CLA) isomers during…”
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    Evaluating acid and base catalysts in the methylation of milk and rumen fatty acids with special emphasis on conjugated dienes and total trans fatty acids by Kramer, J.K.G, Fellner, V, Dugan, M.E.R, Sauer, F.D, Mossoba, M.M, Yurawecz, M.P

    Published in Lipids (01-11-1997)
    “…Milk analysis is receiving increased attention. Milk contains conjugated octadecadienoic acids (18∶2) purported to be anticarcinogenic, low levels of essential…”
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    Relative retention order of all isomers of cis/trans conjugated linoleic acid FAME from the 6,8‐ to 13,15‐positions using silver ion HPLC with two elution systems by Delmonte, Pierluigi, Kataoka, Ai, Corl, B. A., Bauman, D. E., Yurawecz, Martin P.

    Published in Lipids (01-05-2005)
    “…CLA, defined as one or more octadecadienoic acids (18∶2) with conjugated double bonds, has been reported to be active in a number of bological systems. GC and…”
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    Effects of Conjugated Linoleic Acid (CLA) Isomers on Oxygen Diffusion−Concentration Products in Liposomes and Phospholipid Solutions by Yin, Jun-Jie, Kramer, John K. G, Yurawecz, Martin P, Eynard, A. R, Mossoba, Magdi M, Yu, Liangli (Lucy)

    Published in Journal of agricultural and food chemistry (20-09-2006)
    “…Conjugated linoleic acids (CLAs) are a group of octadecadienoic acids (18:2) that are naturally present in food products and may have beneficial health…”
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    Preparation, separation, and confirmation of the eight geometrical cis/trans conjugated linoleic acid isomers 8,10- through 11,13-18:2 by Eulitz, K, Yurawecz, M.P, Sehat, N, Fritsche, J, Roach, J.A.G, Mossoba, M.M, Kramer, J.K.G, Adlof, R.O, Ku, Y

    Published in Lipids (01-08-1999)
    “…Conjugated linoleic acid (CLA) mixtures were isomerized with p‐toluenesulfinic acid or I2 catalyst. The resultant mixtures of the eight cis/trans geometric…”
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