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10 in total

1. Hormonal control of ketogenesis. Rapid activation of hepatic ketogenic capacity in fed rats by anti-insulin serum and glucagon.

Authors: J McGarry; P H Wright; D W Foster
Journal: J Clin Invest Date: 1975-06 Impact factor: 14.808

2. 3-Thia fatty acid treatment, in contrast to eicosapentaenoic acid and starvation, induces gene expression of carnitine palmitoyltransferase-II in rat liver.

Authors: L Madsen; R K Berge
Journal: Lipids Date: 1999-05 Impact factor: 1.880

3. Lipids Reprogram Metabolism to Become a Major Carbon Source for Histone Acetylation.

Authors: Eoin McDonnell; Scott B Crown; Douglas B Fox; Betül Kitir; Olga R Ilkayeva; Christian A Olsen; Paul A Grimsrud; Matthew D Hirschey
Journal: Cell Rep Date: 2016-11-01 Impact factor: 9.423

4. Glucose plus insulin regulate fat oxidation by controlling the rate of fatty acid entry into the mitochondria.

Authors: L S Sidossis; C A Stuart; G I Shulman; G D Lopaschuk; R R Wolfe
Journal: J Clin Invest Date: 1996-11-15 Impact factor: 14.808

5. The effect of glucagon treatment and starvation of virgin and lactating rats on the rates of oxidation of octanoyl-L-carnitine and octanoate by isolated liver mitochondria.

Authors: V A Zammit
Journal: Biochem J Date: 1980-08-15 Impact factor: 3.857

6. Metabolic fate of non-esterified fatty acids in isolated hepatocytes from newborn and young pigs. Evidence for a limited capacity for oxidation and increased capacity for esterification.

Authors: J P Pégorier; P H Duée; J Girard; J Peret
Journal: Biochem J Date: 1983-04-15 Impact factor: 3.857

The metabolism of (minus)-octanoylcarnitine in perfused livers from fed and fasted rats. Evidence for a possible regulatory role of carnitine acyltransferase in the control of ketogenesis.

1. Hormonal control of ketogenesis. Rapid activation of hepatic ketogenic capacity in fed rats by anti-insulin serum and glucagon.

2. 3-Thia fatty acid treatment, in contrast to eicosapentaenoic acid and starvation, induces gene expression of carnitine palmitoyltransferase-II in rat liver.

3. Lipids Reprogram Metabolism to Become a Major Carbon Source for Histone Acetylation.

4. Glucose plus insulin regulate fat oxidation by controlling the rate of fatty acid entry into the mitochondria.

5. The effect of glucagon treatment and starvation of virgin and lactating rats on the rates of oxidation of octanoyl-L-carnitine and octanoate by isolated liver mitochondria.

6. Metabolic fate of non-esterified fatty acids in isolated hepatocytes from newborn and young pigs. Evidence for a limited capacity for oxidation and increased capacity for esterification.

7. Glucagon inhibits triacylglycerol synthesis in isolated hepatocytes by lowering their glycerol 3-phosphate content.

8. Effect of nutritional status on the fatty acid composition of rat liver and cultured hepatocytes.

9. Role of carnitine in hepatic ketogenesis.

10. Antiketogenic and hypoglycemic effects of aminocarnitine and acylaminocarnitines.