ライフサイエンスコーパス: metabolizable

1 Materno-fetal clearance of non-metabolizable [(3) H]methyl-d-glucose and placental SLC2

2 We conclude that metabolizable amino acids regulate AMPK in the beta-cell

3 Oocytes were injected with the non-metabolizable analog 3-deaza-cADPR, and cytosolic [Ca(2+

4 ked reversibly by arachidonic acid and a non-metabolizable analog of arachidonic acid, 5,8,11,14-eico

5 In contrast, 2-bromopalmitate, a non-metabolizable analog of palmitate, did not alter the pho

6 as pharmacologically inhibited by the poorly metabolizable analog, betagamma-methylene ATP.

7 Two poorly metabolizable analogs of Ins(1,4,5)P(3), Ins(2,4,5)P(3),

8 However, the non-metabolizable analogue of AA, 5,8,11,14-eicosatetraynoic

9 on plates containing 2-deoxygalactose, a non-metabolizable analogue of galactose.

10 K+ (using 86Rb), taurine, D-aspartate (a non metabolizable analogue of glutamate) and Na+ fluxes duri

11 The results show that high concentrations of metabolizable and nonmetabolizable hexoses activate sign

12 By using both metabolizable and nonmetabolizable sugar substrates of t

13 Both metabolizable and nonmetabolizable sugars induced Incw1-

14 The non-metabolizable C12 analogue 2-bromododecanoic acid was eq

15 al niche that is rich in chitin and/or other metabolizable carbohydrates.

16 ity (as measured fluorometrically by using a metabolizable dye) when stimulated by lipopolysaccharide

17 iciency of use of alcohol for maintenance of metabolizable energy being the same as that for carbohyd

18 ncing explanation for why almonds have a low metabolizable energy content and an attenuated impact on

19 The metabolizable energy content of the almonds was determin

20 The metabolizable energy content of the diets (with suppleme

21 contents, which were corrected for standard metabolizable energy conversion factors.

22 f determining energy needs by using measured metabolizable energy intake (MEI) and TEE.

23 Metabolizable energy intake and changes in total-body en

24 In addition, studies that measured the metabolizable energy of proteins, fats, and carbohydrate

25 in diet (n=16, 17 vs. 8.7 g crude protein/MJ metabolizable energy) from d 0 to 65 gestation (term, ap

26 by olestra to achieve a diet containing 25% metabolizable fat).

27 nsible for triggering Ca2+ entry since a non-metabolizable form of dodecanoic acid (2-bromododecanoic

28 nose, and 2-deoxyglucose, but not by the non-metabolizable glucose analog, 3-O-methylglucose.

29 mentation with 2-deoxy-D-glucose (2DG) a non-metabolizable glucose analog.

30 D-glucose and was unresponsive to KCl or non-metabolizable glucose analogs in MIN6 beta-cells.

31 cetyl-D-glucosamine, and mimicked by the non-metabolizable glucose analogue 2-deoxyglucose, but not b

32 primary cultures are also excited by the non-metabolizable glucose analogue alpha-methylglucopyranosi

33 In turn, 2-deoxyglucose, a non-metabolizable glucose analogue, elicited larger response

34 , in cells starved of sugars or fed with non-metabolizable glucose analogues, all 14-3-3 binding was

35 und that RyaA synthesis was induced by a non-metabolizable glucose phosphate analogue and was necessa

36 Accumulation of non-metabolizable glucose-phosphate in Escherichia coli is g

37 mine or by 6-diazo-5-oxo-l-norleucine, a non-metabolizable glutamine analogue.

38 as observed when cells were grown on readily metabolizable hexoses.

39 -inositol 4,5-bisphosphate (gPIP2), a poorly metabolizable IP3 analog, led to less well localized rel

40 ncreased by conversion of sucrose into a non-metabolizable isomer.

41 tuitous induction of the lac operon with non-metabolizable lactose analogues generates an all-or-noth

42 Therefore, bioaccumulation factors for metabolizable lipophilic contaminants may be higher in A

43 are regulated by the availability of rapidly metabolizable nitrogen sources, but not by any mechanism

44 consists of stable droplets (<250 nm) of the metabolizable oil squalene and two surfactants, polyoxye

45 partly by the absence of renal excretion of metabolizable organic anions, leaving only the nonmetabo

46 in Pi-starved pdr2 by phosphite (Phi), a non-metabolizable Pi analog, and divided-root experiments su

47 ed circulating progesterone and suggests non-metabolizable progestogen might represent an alternative

48 etary methionine (1.89 Met vs. 2.43 Met % of metabolizable protein) from calving until embryo flushin

49 ted by high concentrations of any of several metabolizable PTS sugars.

50 by the lac repressor and induced by the non-metabolizable substrate IPTG.

51 Moreover, when given a choice between metabolizable sugar (sucrose or D-glucose) and nonmetabo

52 s conditional and depends on the presence of metabolizable sugar in the growth medium.

53 In combination with low nitrogen supply, metabolizable sugars (glucose, fructose, or sucrose) ind

54 SgrS is expressed when non-metabolizable sugars accumulate intracellularly (glucose

55 e FR fluence rate and on the availability of metabolizable sugars in the growth medium.

56 uction of expression of H(+)-ATPase genes by metabolizable sugars may be part of a generalized cellul

57 When glucose or other rapidly metabolizable sugars were present in the medium, the sta

58 However, only the metabolizable sugars, sucrose and D-glucose, were associ

59 starved Gr5a; Gr64a double mutants preferred metabolizable sugars.