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1                                              CDP-choline also elevated hypothalamic extracellular tot
2                                              CDP-choline also provided significant protection for hip
3                                              CDP-choline caused a dose- and time-dependent increase i
4                                              CDP-choline liposomes deliver the agent intact to the br
5                                              CDP-choline restored cardiolipin levels, arachidonic aci
6                                              CDP-choline treatment significantly attenuated PLA2 acti
7                                              CDP-choline treatment significantly attenuated the infar
8 ndicate that Sec14p functions to alleviate a CDP-choline pathway-mediated toxicity to yeast Golgi sec
9  this raises the possibility that they use a CDP-choline pathway for the biosynthesis of phosphatidyl
10                     One of the enzymes was a CDP-choline pyrophosphatase, the first Nudix hydrolase a
11                          Brain UTP, CTP, and CDP-choline were all elevated 15 min after UMP (from 254
12 line, uridine (a precursor for UTP, CTP, and CDP-choline), and a PUFA (e.g., docosahexaenoic acid); m
13 h catalyzes the synthesis of PC from DAG and CDP-choline.
14 the phosphatidylethanolamine methylation and CDP-choline pathways are not responsible for generating
15 r in P. falciparum, thus making the SDPM and CDP-choline pathways the only routes for phosphatidylcho
16  significant elevations in UTP, CT, USAP and CDP-choline levels in PC12 cells.
17 e identify other possible substrates such as CDP-choline, ATP, and ADP.
18  UMP dose that significantly increased brain CDP-choline was 0.05 mmol/kg.
19 nal step of PtdCho synthesis is catalyzed by CDP-choline:1,2-diacylglycerol cholinephosphotransferase
20 n the suppression of the sec14(ts) defect by CDP-choline pathway mutations, indicating a role for pho
21  PtdCho, which was significantly restored by CDP-choline treatment.
22 ha protein, which were partially restored by CDP-choline.
23 f CCT activity, the accumulation of cellular CDP-choline, and enhanced radiolabeling of phosphatidylc
24  present in cytidine 5'-diphosphate choline (CDP-choline), are major precursors of the phosphatidylch
25 oline into the cytidine diphosphate-choline (CDP-choline) PC biosynthetic pathway relative to betaine
26 nthesis of phosphatidylcholine from choline (CDP-choline pathway), the parasite synthesizes this majo
27  T. denticola does contain a licCA-dependent CDP-choline pathway for phosphatidylcholine biosynthesis
28 hosphatidylcholine through a licCA-dependent CDP-choline pathway identified only in the genus Trepone
29 m radiolabeled cytidine 5'-diphosphocholine (CDP-choline) in HCCs.
30 rdic effect of cytidine 5'-diphosphocholine (CDP-choline).
31                Cytidine-5'-diphosphocholine (CDP-choline, Citicoline, Somazina) is in clinical use (i
32 se enzymes in the cytidine diphosphocholine (CDP-choline) pathway of PtdCho biosynthesis.
33 onents of the liposomes and the encapsulated CDP-choline.
34 kely to inhibit the conversion of endogenous CDP-choline to PC.
35 ; this enhances the production of endogenous CDP-choline which then combines with fatty acids (as dia
36 cell survival questions whether endonuclear, CDP-choline pathway phosphatidylcholine synthesis may oc
37 ance PC synthesis, we developed an assay for CDP-choline, an immediate and rate-limiting precursor in
38 phosphate from CTP to phosphocholine to form CDP-choline.
39 62%) compared to the equivalent dose of free CDP-choline (by 26%) after 1 h focal cerebral ischemia a
40  in vitro phosphatidylcholine formation from CDP-choline and diacylglycerol, and full activity requir
41 ne caused concentration-related increases in CDP-choline levels, and that this effect was mediated by
42 ransferase (lyso-PAF-AT) and DTT-insensitive CDP-choline 1-alkyl-2-acetyl-sn-glycerol cholinephosphot
43      The structures of apo-LicC and the LicC-CDP-choline-Mg(2+) ternary complex were determined, and
44 line cytidylyltransferase (CCT), which makes CDP-choline.
45                            Administration of CDP-choline to rats increases blood and brain cytidine a
46                       Oral administration of CDP-choline to rats raises plasma and brain cytidine lev
47 erebroventricular (i.c.v.) administration of CDP-choline was made and blood pressure and heart rate w
48      However, the mechanism of conversion of CDP-choline to phosphatidylcholine remained unclear.
49 ould contribute to the beneficial effects of CDP-choline in treating stroke or other brain damage.
50                        Beneficial effects of CDP-choline liposomes in stroke may derive from a synerg
51  Bacillus cereus catalyzes the hydrolysis of CDP-choline to produce CMP and phosphocholine.
52 s inhibitor] 5 min prior to the injection of CDP-choline to determine the effects of these inhibitors
53      CCT1 exhibited a V max of 23904 nmol of CDP-choline min (-1) mg (-1) and apparent K m values for
54  a uridine source, enhances the synthesis of CDP-choline, the immediate precursor of PC, in gerbil br
55                  In contrast, in humans oral CDP-choline increases plasma levels of uridine.
56 n of [methyl-3H]choline into phosphocholine, CDP-choline, and phosphatidylcholine in cells carrying t
57 ly that includes the enzymes that synthesize CDP-choline and CDP-ethanolamine for phosphatidylcholine
58                   Finally, we determine that CDP-choline pathway activity contributes to the inositol
59                           Our data show that CDP-choline liposomes significantly (P < 0.01) decreased
60      Immunohistochemical studies showed that CDP-choline increased COX-1 and -2 immunoreactivities in
61                           Others showed that CDP-choline liposomes significantly increased brain upta
62                     The results suggest that CDP-choline may stimulate prostaglandin synthesis throug
63                      These data suggest that CDP-choline prevented the activation of phospholipase A(
64   Taken together, these results suggest that CDP-choline significantly restores Ptd-Cho levels by dif
65                                          The CDP-choline then condenses with diacylglycerol (DAG) to
66 found distinction in PC profiles between the CDP-choline pathway and the PE methylation pathway.
67 se of choline for PC production via both the CDP-choline and PEMT pathways shows the substantial dema
68 synthesis of phosphatidylcholine (PC) by the CDP-choline (Kennedy) pathway.
69    Phospho-choline is converted to PC by the CDP-choline pathway, explaining the phenotype conferred
70 tion of phosphatidylcholine synthesis by the CDP-choline pathway.
71 otein kinase A regulates PC synthesis by the CDP-choline pathway.
72 cant fate for this DAG is consumption by the CDP-choline pathway.
73  the synthesis of phosphatidylcholine by the CDP-choline pathway.
74 d membranes and is synthesised mainly by the CDP-choline pathway.
75               PC molecules produced from the CDP-choline pathway were mainly comprised of medium chai
76 te and were more diverse than those from the CDP-choline pathway.
77           As the rate-limiting enzyme in the CDP-choline pathway for PC synthesis, CTP:phosphocholine
78                   In yeast, mutations in the CDP-choline pathway for phosphatidylcholine biosynthesis
79 line by ATP, the first committed step in the CDP-choline pathway for phosphatidylcholine biosynthesis
80      Mutations (cki1, cct1, and cpt1) in the CDP-choline pathway for phosphatidylcholine synthesis su
81 rase (CT) is the rate-limiting enzyme in the CDP-choline pathway of PC biosynthesis, which is utilize
82 esis of CCT, the rate-limiting enzyme in the CDP-choline pathway, is elevated in fibroblasts overexpr
83 eport that strains carrying mutations in the CDP-choline pathway, such as cki1, exhibit a choline exc
84 se (CCT), the second of three enzymes in the CDP-choline pathway, which is used to synthesize phospha
85 le detectable impact on the operation of the CDP-choline metabolic pathway in adult tissues.
86 uirement is abrogated by inactivation of the CDP-choline pathway for phosphatidylcholine biosynthesis
87 e to phosphocholine as the first step of the CDP-choline pathway for the biosynthesis of phosphatidyl
88 ng that XBP-1(S) increases the output of the CDP-choline pathway primarily via its effects on CCT.
89 to distinguish the products from that of the CDP-choline pathway.
90 this phospholipid occurs via two routes, the CDP-choline pathway, which uses host choline as a precur
91 synthesis of phosphatidylcholine through the CDP-choline pathway.
92 is in the brain is predominantly through the CDP-choline pathway.
93                           In addition to the CDP-choline pathway for phosphatidylcholine (PC) synthes
94                While the contribution to the CDP-choline pathway remained intact in hepatocarcinoma c
95 the synthesis of phosphatidylcholine via the CDP-choline branch of the Kennedy pathway.
96 sis both as an intact choline moiety via the CDP-choline pathway and as a methyl donor via PE methyla
97 dylethanolamine or from free choline via the CDP-choline pathway.
98 le for phosphatidylcholine synthesis via the CDP-choline pathway.
99  of phosphatidylcholine biosynthesis via the CDP-choline pathway.
100 (CCT), the rate-regulatory enzyme within the CDP-choline pathway, by 40% compared with control, but i
101 f choline to form choline phosphate and then CDP-choline.
102 First, membrane-free nuclei retain all three CDP-choline pathway enzymes in proportions comparable wi
103 holine and cytidine 5'-triphosphate (CTP) to CDP-choline for the eventual synthesis of phosphatidylch
104 holine and cytidine 5'-triphosphate (CTP) to CDP-choline for the subsequent synthesis of phosphatidyl
105 ked the pressor and bradycardic responses to CDP-choline while neomycine or furegrelate partially att
106 se inhibitors on cardiovascular responses to CDP-choline.
107 his phosphocholine transferase activity used CDP-choline as a substrate and required a conserved hist
108               Our data support a model where CDP-choline hydrolysis is catalyzed by the enclosed Nudi
109                               Treatment with CDP-choline ameliorated SAND, suggesting that it may be

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