ライフサイエンスコーパス: glycogenolytic

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1 EPI markedly decreased (60-80%) its overall glycogenolytic action on the liver.

2 ct rapidly with bGP and readily inhibits its glycogenolytic activity (kinact = 1.4 x 10(5) m(-1) s(-1

3 ons and neurodegeneration, impairment of the glycogenolytic activity of bGP by DTCs such as thiram ma

4 esponse to insulin, whereas, conversely, the glycogenolytic agent isoproterenol increased cytosolic e

5 ubation of pretreated 3T3-L1 adipocytes with glycogenolytic agents reversed the desensitization event

6 Furthermore, glycogenolytic agents such as forskolin or glucagon are

7 ng, leading to reduced expression of hepatic glycogenolytic and gluconeogenic genes.

8 ation, a downregulation of expression of the glycogenolytic and glycolytic enzymes in muscle that med

9 exercise induces decreases in expression of glycogenolytic and glycolytic enzymes in rat skeletal mu

10 of contributions of the 13 reactions of the glycogenolytic and glycolytic network to total proton lo

11 These data support the observation that glycogenolytic and glycolytic rates are elevated in vivo

12 Skeletal muscle glycogenolytic ATP production, measured during the first

13 take by the liver, and from a redirection of glycogenolytic carbon to lactate rather than glucose.

14 4%, respectively, of the EGP (NS); absolute glycogenolytic contribution to the EGP was 15 +/- 2, 11

15 ional suppression of key gluconeogenetic and glycogenolytic enzymes, phosphoenolpyruvate carboxykinas

16 lag and subsequent efflux of glycolytic and glycogenolytic enzymes.

17 sked by the hormone's effects on net hepatic glycogenolytic flux and the resulting changes in glycoly

18 unted in the KO mice because of a diminished glycogenolytic flux.

19 patocytes respond to physiological levels of glycogenolytic hormones with well-characterized intracel

20 in EGP results entirely from a reduction of glycogenolytic input into blood glucose, and the duratio

21 tribution from both oxidative and glycolytic/glycogenolytic metabolism.

22 terminal step in both the gluconeogenic and glycogenolytic pathways and is opposed by the glycolytic

23 data indicate that appropriate activation of glycogenolytic pathways is obligatory for normal metabor

24 ate, the final step in the gluconeogenic and glycogenolytic pathways.

25 s the terminal step in the gluconeogenic and glycogenolytic pathways.

26 s the terminal step in the gluconeogenic and glycogenolytic pathways.

27 yzes the final step in the gluconeogenic and glycogenolytic pathways.

28 The net hepatic glycogenolytic rate decreased from 1.72 +/- 0.20 to -0.2

29 Maximal in vivo glycogenolytic rates of 207 +/- 48 mM ATP min-1 were obt

30 Both [13C]glycolytic and [13C]glycogenolytic rates were significantly lower during tot

31 /R(Gl)-overexpressing cells exhibit a strong glycogenolytic response to forskolin, whereas PTG-overex

32 exhibited impairment in one or both of these glycogenolytic signaling pathways.

33 of glycogenic potency and responsiveness to glycogenolytic signals that allows it to be used to lowe

34 gen metabolism in response to glycogenic and glycogenolytic signals.

35 roducts distinguished the gluconeogenic from glycogenolytic state in these functioning livers.

36 y distinguish livers in a gluconeogenic from glycogenolytic state.

37 ned to establish either a gluconeogenic or a glycogenolytic state.

38 support the use of CP-91149 in investigating glycogenolytic versus gluconeogenic flux in hepatic gluc

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