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153 related items for PubMed ID: 7782307

  • 1. Gluconeogenesis and intrahepatic triose phosphate flux in response to fasting or substrate loads. Application of the mass isotopomer distribution analysis technique with testing of assumptions and potential problems.
    Neese RA, Schwarz JM, Faix D, Turner S, Letscher A, Vu D, Hellerstein MK.
    J Biol Chem; 1995 Jun 16; 270(24):14452-66. PubMed ID: 7782307
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  • 2. The effect of fasting and fructose and glucose infusion on gluconeogenesis and triose phosphate flux in rats in vivo.
    Wolf G.
    Nutr Rev; 1995 Oct 16; 53(10):299-301. PubMed ID: 8584289
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  • 3. Limitations of the mass isotopomer distribution analysis of glucose to study gluconeogenesis. Substrate cycling between glycerol and triose phosphates in liver.
    Previs SF, Fernandez CA, Yang D, Soloviev MV, David F, Brunengraber H.
    J Biol Chem; 1995 Aug 25; 270(34):19806-15. PubMed ID: 7649990
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  • 4. Sources of plasma glucose and liver glycogen in fasted ob/ob mice.
    Turner SM, Linfoot PA, Neese RA, Hellerstein MK.
    Acta Diabetol; 2005 Dec 25; 42(4):187-93. PubMed ID: 16382307
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  • 5. Measuring glycerol turnover, gluconeogenesis from glycerol, and total gluconeogenesis with [2-13C] glycerol: role of the infusion-sampling mode.
    Peroni O, Large V, Odeon M, Beylot M.
    Metabolism; 1996 Jul 25; 45(7):897-901. PubMed ID: 8692028
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  • 8. Isotopomer studies of gluconeogenesis and the Krebs cycle with 13C-labeled lactate.
    Katz J, Wals P, Lee WN.
    J Biol Chem; 1993 Dec 05; 268(34):25509-21. PubMed ID: 7902352
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  • 9. Altered fluxes responsible for reduced hepatic glucose production and gluconeogenesis by exogenous glucose in rats.
    Hellerstein MK, Neese RA, Schwarz JM, Turner S, Faix D, Wu K.
    Am J Physiol; 1997 Jan 05; 272(1 Pt 1):E163-72. PubMed ID: 9038866
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  • 10. Measuring gluconeogenesis with [2-13C]glycerol and mass isotopomer distribution analysis of glucose.
    Peroni O, Large V, Beylot M.
    Am J Physiol; 1995 Sep 05; 269(3 Pt 1):E516-23. PubMed ID: 7573429
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  • 13. Measurement of hepatic Ra UDP-glucose in vivo in rats: relation to glycogen deposition and labeling patterns.
    Hellerstein MK, Letscher A, Schwarz JM, César D, Shackleton CH, Turner S, Neese R, Wu K, Bock S, Kaempfer S.
    Am J Physiol; 1997 Jan 05; 272(1 Pt 1):E155-62. PubMed ID: 9038865
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  • 14. Glycerol not lactate is the major net carbon source for gluconeogenesis in mice during both short and prolonged fasting.
    Wang Y, Kwon H, Su X, Wondisford FE.
    Mol Metab; 2020 Jan 05; 31():36-44. PubMed ID: 31918920
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  • 15. A limitation in the use of mass isotopomer distributions to measure gluconeogenesis in fasting humans.
    Landau BR, Fernandez CA, Previs SF, Ekberg K, Chandramouli V, Wahren J, Kalhan SC, Brunengraber H.
    Am J Physiol; 1995 Jul 05; 269(1 Pt 1):E18-26. PubMed ID: 7631774
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  • 16. Effects of fasting and glucocorticoids on hepatic gluconeogenesis assessed using two independent methods in vivo.
    Goldstein RE, Rossetti L, Palmer BA, Liu R, Massillon D, Scott M, Neal D, Williams P, Peeler B, Cherrington AD.
    Am J Physiol Endocrinol Metab; 2002 Nov 05; 283(5):E946-57. PubMed ID: 12376321
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  • 18. Gluconeogenesis and hepatic glycogenolysis during exercise at the lactate threshold.
    Emhoff CA, Messonnier LA, Horning MA, Fattor JA, Carlson TJ, Brooks GA.
    J Appl Physiol (1985); 2013 Feb 05; 114(3):297-306. PubMed ID: 23239870
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  • 20. The inhibition of gluconeogenesis following alcohol in humans.
    Siler SQ, Neese RA, Christiansen MP, Hellerstein MK.
    Am J Physiol; 1998 Nov 05; 275(5):E897-907. PubMed ID: 9815011
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