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1 at this defect can be rescued by addition of isopentenyl pyrophosphate.
2 te that causes intracellular accumulation of isopentenyl pyrophosphate.
3 ydroxy-3-methyl-but-2-enyl pyrophosphate and isopentenyl pyrophosphate.
4 ough upstream accumulation of the cognate Ag isopentenyl pyrophosphate.
5 e Vdelta2 gammadelta T-cell receptor agonist isopentenyl pyrophosphate.
6  alternating C2 and C3 units, rather than C5 isopentenyl pyrophosphate.
7 hat condenses farnesyl diphosphate (FDP) and isopentenyl pyrophosphate.
8 pheral blood after stimulation in vitro with isopentenyl pyrophosphate.
9 te, and isomeric dimethylallyl pyrophosphate/isopentenyl pyrophosphate.
10 the biosynthesis of the isoprenoid precursor isopentenyl pyrophosphate, 1-deoxy-D-xylulose-5-phosphat
11 on of mevalonate 5-diphosphate (MDP) to form isopentenyl pyrophosphate, a ubiquitous precursor for is
12 thesis pathway responsible for production of isopentenyl-pyrophosphate, a short-chain phospholipid th
13 P), a microbial isoprenoid intermediate, and isopentenyl pyrophosphate, an endogenous isoprenoid inte
14 genesis in the first cycle and is rescued by isopentenyl pyrophosphate, an essential apicoplast produ
15 ylerythritol-phosphate (MEP) pathway forming isopentenyl pyrophosphate and a heterologous downstream
16 , pulsing of BZ-(C)-C(5)-OPP is inhibited by isopentenyl pyrophosphate and an inactive analog, sugges
17 cellular accumulation of the phosphoantigens isopentenyl pyrophosphate and ApppI.
18 mulation with prenyl pyrophosphate antigens (isopentenyl pyrophosphate and monomethyl phosphate).
19 madelta T cells have been shown to recognize isopentenyl pyrophosphate and related structures and hum
20 ed reactivity to the prenyl pyrophosphate Ag isopentenyl pyrophosphate and to its synthetic analogue
21 ood gamma delta T cells to the nonpeptide Ag isopentenyl pyrophosphate and to its synthetic analogue
22 s Ag-nonreactive TCR destroyed reactivity to isopentenyl pyrophosphate and to the mycobacterial super
23 nic lines showed a three-fold enhancement of isopentenyl pyrophosphate, and targeting AACPR, DBR2, an
24              Quantification of intracellular isopentenyl pyrophosphate/ApppI following ZOL treatment
25 inity of 1.1 muM, whereas the endogenous pAg isopentenyl pyrophosphate binds with an affinity of 627
26 rget HCC cell lines sensitised to accumulate isopentenyl-pyrophosphate by the aminobisphosphonate Zol
27 mportant accessory cells that provide the Ag isopentenyl pyrophosphate, CD56(bright)CD11c(+) NK cells
28  of TRPA1, being inhibited by ruthenium red, isopentenyl pyrophosphate, HC-030031, A967079 or TRPA1 k
29                        Curcumin also blocked isopentenyl pyrophosphate-induced activation of NF-kappa
30  levels > or =30 microM profoundly inhibited isopentenyl pyrophosphate-induced release of the chemoki
31              20.1 stimulation was not due to isopentenyl pyrophosphate (IPP) accumulation because 20.
32 zation of the two ubiquitous isoprene units, isopentenyl pyrophosphate (IPP) and dimethylallyl pyroph
33 e all derived from the 5-carbon diphosphates isopentenyl pyrophosphate (IPP) and dimethylallyl pyroph
34 ginates from two five-carbon (C(5)) isomers, isopentenyl pyrophosphate (IPP) and dimethylallyl pyroph
35                                              Isopentenyl pyrophosphate (IPP) is a common precursor fo
36                                              Isopentenyl pyrophosphate (IPP) is an essential metaboli
37                                   The enzyme isopentenyl pyrophosphate (IPP) isomerase catalyzes the
38 amma-dimethylallyl pyrophosphate (DMAPP) and isopentenyl pyrophosphate (IPP) to all of the known terp
39 the recombinant truncated AaIPPI1 isomerized isopentenyl pyrophosphate (IPP) to dimethyl allyl pyroph
40 e synthesised via sequential condensation of isopentenyl pyrophosphate (IPP) to dimethylallyl pyropho
41 at catalyzes the reversible isomerization of isopentenyl pyrophosphate (IPP) to dimethylallyl pyropho
42 required for haem biosynthesis-doubles as an isopentenyl pyrophosphate (IPP) transporter in Saccharom
43                                    When [14C]isopentenyl pyrophosphate (IPP) was used as the substrat
44 nsecutive condensation of eight molecules of isopentenyl pyrophosphate (IPP) with farnesyl pyrophosph
45                Furthermore, stimulation with isopentenyl pyrophosphate (IPP), a metabolite in the mev
46                      The results showed that isopentenyl pyrophosphate (IPP), a soluble phospholigand
47 ol-4-phosphate pathway used by microbes, and isopentenyl pyrophosphate (IPP), an intermediate in the
48  encoding early steps in the biosynthesis of isopentenyl pyrophosphate (IPP), the precursor of all is
49 ynthesized from the five-carbon starter unit isopentenyl pyrophosphate (IPP).
50 present only a subset of the phosphoantigen {isopentenyl pyrophosphate [IPP] and (E)-4-hydroxy-3-meth
51 sphate (HMBPP) or endogenous pyrophosphates (isopentenyl pyrophosphate [IPP]).
52 -2-enyl pyrophosphate, HMBPP] or endogenous (isopentenyl pyrophosphate, IPP) and PAg sensing depends
53                  In this study, we cloned an isopentenyl pyrophosphate isomerase (IPPI) cDNA, AaIPPI1
54                              By knocking out isopentenyl pyrophosphate isomerase (IPPI) expression, w
55 onophosphate kinase superfamily, and between isopentenyl pyrophosphate isomerases and MutT pyrophosph
56  by nonpeptidic monoalkyl phosphates such as isopentenyl pyrophosphate leads to the up-regulation of
57 ay, catalyzes the successive condensation of isopentenyl pyrophosphate with dimethylallyl pyrophospha
58 ethylerythritol phosphate pathway to produce isopentenyl pyrophosphate with more favorable thermodyna