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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 free glutamic and aspartic acid, and choline glycerophosphate.
8 b) ascorbic acid (50 micrograms/ml) and beta-glycerophosphate (10 mM); or c) ascorbic acid, beta-glyc
9  P/L) or the same formula with added calcium glycerophosphate (1800 mg Ca and 1390 mg P/L) for 9 mo.
10  P/L) or the same formula with added calcium glycerophosphate (1800 mg Ca and 1390 mg P/L) for 9 mo.
11  as well as the site which may bind the poly(glycerophosphate) acceptor moiety of membrane-associated
12                        The topography of rat glycerophosphate acyltransferase (GAT) in the transverse
13 3-phosphate (GP), which is then converted by glycerophosphate acyltransferase (GPAT) to 1-acyl-GP.
14 or ERRa-regulated NAFLD/NASH development and glycerophosphate acyltransferase 4 was identified as a n
15 polymyxin B-agarose stimulated mitochondrial glycerophosphate acyltransferase activity approximately
16 ented that four gene families, including the glycerophosphate acyltransferases (GPATs), acylglyceroph
17     Lysophosphatidic acid (LPA), plasmalogen-glycerophosphate (alkenyl-GP) and, cyclic-phosphatidic a
18 sphatase to a similar magnitude as does beta-glycerophosphate alone.
19 e dihydroxyacetone phosphate (DHAP) to alpha-glycerophosphate (alpha-GP) ratio significantly increase
20 ere cultured in medium containing 10 mM beta-glycerophosphate and 50 mug/ml ascorbic acid to induce m
21 hen cells were grown in the presence of beta-glycerophosphate and ascorbic acid.
22 phosphate (10 mM); or c) ascorbic acid, beta-glycerophosphate and DEX (100 nM) for 30 days.
23 uscle extract that generates pulses of alpha-glycerophosphate and pyruvate and induces oscillations i
24 from ePTFE membranes were cultured with beta-glycerophosphate and the test agents for 2 to 5 weeks, a
25 SG), glycolytic intermediates, malate, alpha-glycerophosphate, and adenine nucleotides were assayed i
26 scal cells cultured with ascorbic acid, beta-glycerophosphate, and dexamethasone supplementation to s
27 te, glutamate, malate, dihydroorotate, alpha-glycerophosphate, and N,N,N',N'-tetramethyl-p-phenylened
28 nce of L-Trp with NaCl and/or disodium alpha-glycerophosphate are more difficult to interpret in term
29                                          The glycerophosphate backbone for triglyceride synthesis is
30 ntermediate in the biosynthesis of the major glycerophosphate-based phospholipids of prokaryotes and
31 bic acid (Asc), dexamethasone (Dex) and beta-glycerophosphate (beta-Gly) are commonly used to promote
32 ddition of the organic phosphate donor, beta-glycerophosphate (betaGP).
33 onformation in the absence of disodium alpha-glycerophosphate but was able to form a closed conformat
34 nner ear drug delivery system using chitosan glycerophosphate (CGP) hydrogel loaded with drugs common
35                                        alpha-glycerophosphate complex and the rate constant for reduc
36  Cyclic phosphatidic acid (1-acyl-2,3-cyclic-glycerophosphate, CPA), one of nature's simplest phospho
37 sion of dihydroxyacetone phosphate (DHAP) by glycerophosphate dehydrogenase (GPD) to sn-glycerol 3-ph
38 yme histochemistry for menadione-dependent a-glycerophosphate dehydrogenase (M-a-GPDH) (to label angi
39 omeostasis or 2) inhibition of mitochondrial glycerophosphate dehydrogenase (mGPDH) and thereby atten
40      Enzyme histochemistry showed high alpha glycerophosphate dehydrogenase activity in poorly differ
41 d to exhibit adipocyte morphology, to induce glycerophosphate dehydrogenase activity, and to induce d
42 cal to that of the membrane-associated alpha-glycerophosphate dehydrogenase from Bacillus subtilis; o
43 ucleotide knockdown of hepatic mitochondrial glycerophosphate dehydrogenase in rats resulted in a phe
44  were replicated in whole-body mitochondrial glycerophosphate dehydrogenase knockout mice.
45 ibits the redox shuttle enzyme mitochondrial glycerophosphate dehydrogenase, resulting in an altered
46 ce is 30-43% identical to those of the alpha-glycerophosphate dehydrogenases (GlpDs) from mitochondri
47 is completely absent in the homologous alpha-glycerophosphate dehydrogenases.
48 arboxylic acids to provide the corresponding glycerophosphate derivatives.
49 ted for 10 days with osteogenic media (+beta-glycerophosphate) exhibited similar osteoinductivity to
50  inorganic phosphate, but not by UTP or beta-glycerophosphate, fully in line with the respective inva
51                             We conclude that glycerophosphate generation may be as important as NADPH
52 ecies measured were glycerophosphoinositols, glycerophosphates, glycerolphosphoglycerols, glycerophos
53 ethasone (Dex), ascorbic acid (AA), and beta-glycerophosphate (GP), they underwent sequential differe
54 e a network of eight hydrogen bonds with the glycerophosphate head group of its LPA antigen.
55  doses of dexamethasone, ascorbic acid, beta-glycerophosphate, heparin, retinoic acid and vitamin D a
56 in the presence or absence of disodium alpha-glycerophosphate, indicating the preference for a closed
57 uated the inhibitory effect of IGF-I on beta-glycerophosphate-induced mineralization (p < 0.05) and a
58 /ml) significantly protected VSMCs from beta-glycerophosphate-induced osteogenic differentiation (p <
59 1 to 1.7:1, suggesting that glycogen-derived glycerophosphate is important in triacylglycerides synth
60 mineralization is accelerated, although beta-glycerophosphate is still required for this effect.
61 ed hydrogel, ionically crosslinked with beta-glycerophosphate, is optimised to obtain sol/gel transit
62 ed transfer of oleic acid from oleoyl-CoA to glycerophosphate, lysophosphatidic acid, or diacylglycer
63 consistent with a pyridinium molecule with a glycerophosphate moiety.
64 7 of LPA(1-3) predicted to interact with the glycerophosphate motif of LPA C18:1.
65 the identification of a series of methylated glycerophosphates never previously observed in grapes.
66 eracea L.) enzyme was stabilized by DL-alpha-glycerophosphate or ethanol and destabilized by D-ribulo
67      The addition of the TrpA ligands, alpha-glycerophosphate or indoleglycerol phosphate, during cat
68  MVs, whereas phosphomonoesters such as beta-glycerophosphate or phosphoethanolamine had no effect.
69 e whether changes in Ca2+ and possibly alpha-glycerophosphate or pyruvate supply could underlie obser
70 glutamate, isocitrate, dihydroorotate, alpha-glycerophosphate, or endogenous substrates.
71                      The FAD-dependent alpha-glycerophosphate oxidase (GlpO) from Enterococcus cassel
72 ne previously uncharacterized protein, alpha-glycerophosphate oxidase (GlpO), was cytotoxic for human
73               The soluble flavoprotein alpha-glycerophosphate oxidase from Enterococcus casseliflavus
74                        The recombinant alpha-glycerophosphate oxidase is fully active and stabilizes
75                      Surprisingly, the alpha-glycerophosphate oxidase sequence is 43% identical to th
76  reported previously, the flavoprotein alpha-glycerophosphate oxidases (GlpOs) from a number of enter
77 cyltransferases (DGATs), are involved in the glycerophosphate pathway of de novo triglyceride (TG) bi
78  the sequences of gene family members in the glycerophosphate pathway were obtained by screening the
79 mbinations of squalene (SQ) and phosphatidyl glycerophosphate (PGP) which act synergistically.
80               The addition of disodium alpha-glycerophosphate produced a signal twice as intense, sug
81 erol is not acting as a cosubstrate since no glycerophosphate product was detectable.
82       Metformin inhibits complex I and alpha-glycerophosphate shuttle, and the resultant increase in
83 iting dephosphorylation of PIP(2) using beta-glycerophosphate slowed rundown by nearly 3-fold.
84 n lactate), and a 9.2-fold increase in alpha-glycerophosphate suggest diabetes-induced inhibition of
85 o period we cannot conclude that the calcium glycerophosphate supplement prevented lead absorption in
86 ntified, perhaps a unique substituent, alpha-glycerophosphate, which is attached to Ser93 by a phosph
87 he mitochondrial and microsomal acylation of glycerophosphate with palmitoyl-CoA-agarose was 80-100%