ライフサイエンスコーパス: glycerophosphate

1 nformation in the presence of disodium alpha-glycerophosphate.

2 c ligands sodium chloride and disodium alpha-glycerophosphate.

3 SQC signal in the presence of disodium alpha-glycerophosphate.

4 m in the energy-yielding metabolism of alpha-glycerophosphate.

5 ely high concentrations of pyruvate or alpha-glycerophosphate.

6 ich was cultured with ascorbic acid and beta-glycerophosphate.

7 b) ascorbic acid (50 micrograms/ml) and beta-glycerophosphate (10 mM); or c) ascorbic acid, beta-glyc

8 P/L) or the same formula with added calcium glycerophosphate (1800 mg Ca and 1390 mg P/L) for 9 mo.

9 P/L) or the same formula with added calcium glycerophosphate (1800 mg Ca and 1390 mg P/L) for 9 mo.

10 as well as the site which may bind the poly(glycerophosphate) acceptor moiety of membrane-associated

11 The topography of rat glycerophosphate acyltransferase (GAT) in the transverse

12 3-phosphate (GP), which is then converted by glycerophosphate acyltransferase (GPAT) to 1-acyl-GP.

13 polymyxin B-agarose stimulated mitochondrial glycerophosphate acyltransferase activity approximately

14 Lysophosphatidic acid (LPA), plasmalogen-glycerophosphate (alkenyl-GP) and, cyclic-phosphatidic a

15 sphatase to a similar magnitude as does beta-glycerophosphate alone.

16 e dihydroxyacetone phosphate (DHAP) to alpha-glycerophosphate (alpha-GP) ratio significantly increase

17 ere cultured in medium containing 10 mM beta-glycerophosphate and 50 mug/ml ascorbic acid to induce m

18 hen cells were grown in the presence of beta-glycerophosphate and ascorbic acid.

19 phosphate (10 mM); or c) ascorbic acid, beta-glycerophosphate and DEX (100 nM) for 30 days.

20 uscle extract that generates pulses of alpha-glycerophosphate and pyruvate and induces oscillations i

21 from ePTFE membranes were cultured with beta-glycerophosphate and the test agents for 2 to 5 weeks, a

22 SG), glycolytic intermediates, malate, alpha-glycerophosphate, and adenine nucleotides were assayed i

23 scal cells cultured with ascorbic acid, beta-glycerophosphate, and dexamethasone supplementation to s

24 te, glutamate, malate, dihydroorotate, alpha-glycerophosphate, and N,N,N',N'-tetramethyl-p-phenylened

25 nce of L-Trp with NaCl and/or disodium alpha-glycerophosphate are more difficult to interpret in term

26 The glycerophosphate backbone for triglyceride synthesis is

27 ntermediate in the biosynthesis of the major glycerophosphate-based phospholipids of prokaryotes and

28 ddition of the organic phosphate donor, beta-glycerophosphate (betaGP).

29 onformation in the absence of disodium alpha-glycerophosphate but was able to form a closed conformat

30 nner ear drug delivery system using chitosan glycerophosphate (CGP) hydrogel loaded with drugs common

31 alpha-glycerophosphate complex and the rate constant for reduc

32 Cyclic phosphatidic acid (1-acyl-2,3-cyclic-glycerophosphate, CPA), one of nature's simplest phospho

33 sion of dihydroxyacetone phosphate (DHAP) by glycerophosphate dehydrogenase (GPD) to sn-glycerol 3-ph

34 yme histochemistry for menadione-dependent a-glycerophosphate dehydrogenase (M-a-GPDH) (to label angi

35 Enzyme histochemistry showed high alpha glycerophosphate dehydrogenase activity in poorly differ

36 d to exhibit adipocyte morphology, to induce glycerophosphate dehydrogenase activity, and to induce d

37 cal to that of the membrane-associated alpha-glycerophosphate dehydrogenase from Bacillus subtilis; o

38 ucleotide knockdown of hepatic mitochondrial glycerophosphate dehydrogenase in rats resulted in a phe

39 were replicated in whole-body mitochondrial glycerophosphate dehydrogenase knockout mice.

40 ibits the redox shuttle enzyme mitochondrial glycerophosphate dehydrogenase, resulting in an altered

41 ce is 30-43% identical to those of the alpha-glycerophosphate dehydrogenases (GlpDs) from mitochondri

42 is completely absent in the homologous alpha-glycerophosphate dehydrogenases.

43 ted for 10 days with osteogenic media (+beta-glycerophosphate) exhibited similar osteoinductivity to

44 inorganic phosphate, but not by UTP or beta-glycerophosphate, fully in line with the respective inva

45 We conclude that glycerophosphate generation may be as important as NADPH

46 ecies measured were glycerophosphoinositols, glycerophosphates, glycerolphosphoglycerols, glycerophos

47 ethasone (Dex), ascorbic acid (AA), and beta-glycerophosphate (GP), they underwent sequential differe

48 e a network of eight hydrogen bonds with the glycerophosphate head group of its LPA antigen.

49 doses of dexamethasone, ascorbic acid, beta-glycerophosphate, heparin, retinoic acid and vitamin D a

50 in the presence or absence of disodium alpha-glycerophosphate, indicating the preference for a closed

51 uated the inhibitory effect of IGF-I on beta-glycerophosphate-induced mineralization (p < 0.05) and a

52 /ml) significantly protected VSMCs from beta-glycerophosphate-induced osteogenic differentiation (p <

53 1 to 1.7:1, suggesting that glycogen-derived glycerophosphate is important in triacylglycerides synth

54 mineralization is accelerated, although beta-glycerophosphate is still required for this effect.

55 ed transfer of oleic acid from oleoyl-CoA to glycerophosphate, lysophosphatidic acid, or diacylglycer

56 consistent with a pyridinium molecule with a glycerophosphate moiety.

57 7 of LPA(1-3) predicted to interact with the glycerophosphate motif of LPA C18:1.

58 eracea L.) enzyme was stabilized by DL-alpha-glycerophosphate or ethanol and destabilized by D-ribulo

59 The addition of the TrpA ligands, alpha-glycerophosphate or indoleglycerol phosphate, during cat

60 MVs, whereas phosphomonoesters such as beta-glycerophosphate or phosphoethanolamine had no effect.

61 e whether changes in Ca2+ and possibly alpha-glycerophosphate or pyruvate supply could underlie obser

62 glutamate, isocitrate, dihydroorotate, alpha-glycerophosphate, or endogenous substrates.

63 The FAD-dependent alpha-glycerophosphate oxidase (GlpO) from Enterococcus cassel

64 ne previously uncharacterized protein, alpha-glycerophosphate oxidase (GlpO), was cytotoxic for human

65 The soluble flavoprotein alpha-glycerophosphate oxidase from Enterococcus casseliflavus

66 The recombinant alpha-glycerophosphate oxidase is fully active and stabilizes

67 Surprisingly, the alpha-glycerophosphate oxidase sequence is 43% identical to th

68 reported previously, the flavoprotein alpha-glycerophosphate oxidases (GlpOs) from a number of enter

69 mbinations of squalene (SQ) and phosphatidyl glycerophosphate (PGP) which act synergistically.

70 The addition of disodium alpha-glycerophosphate produced a signal twice as intense, sug

71 erol is not acting as a cosubstrate since no glycerophosphate product was detectable.

72 n lactate), and a 9.2-fold increase in alpha-glycerophosphate suggest diabetes-induced inhibition of

73 o period we cannot conclude that the calcium glycerophosphate supplement prevented lead absorption in

74 ntified, perhaps a unique substituent, alpha-glycerophosphate, which is attached to Ser93 by a phosph

75 he mitochondrial and microsomal acylation of glycerophosphate with palmitoyl-CoA-agarose was 80-100%