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 Here we report a metabolizable binary supracluster (BSC(gal)) that combin

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

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

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

18 o four treatments: (1) basal diet that meets metabolizable energy (ME) and protein (MP) requirements

19 to consider effects of different amounts of metabolizable energy and protein on mammary gland develo

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

21 as the within-participant difference in host metabolizable energy between experimental conditions [Co

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

23 The metabolizable energy content of the almonds was determin

24 The metabolizable energy content of the diets (with suppleme

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

26 0.0001) lost in feces daily and thus, lower metabolizable energy for the host (89.5 +/- 0.73%; range

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

28 Metabolizable energy intake and changes in total-body en

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

30 e substantial interindividual variability in metabolizable energy on the MBD is explained in part by

31 vidual variation in body mass and associated metabolizable energy reserves, although other drivers (e

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

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

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

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

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

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

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

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

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

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

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

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

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

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

46 n the other hand, were found to be much less metabolizable in terms of the number (n = 2) and yields

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

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

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

50 Step changes in concentration of non-metabolizable ligand cause temporary recruitment of stat

51 For metabolizable ligand, the combined effect of sensing and

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

53 Yeast was treated with the non-metabolizable lysophosphatidylcholine analog edelfosine,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

70 starved Gr5a; Gr64a double mutants preferred metabolizable sugars.