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1 hat condenses farnesyl diphosphate (FDP) and 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 pheral blood after stimulation in vitro with isopentenyl pyrophosphate.
8 at this defect can be rescued by addition of isopentenyl pyrophosphate.
9 the biosynthesis of the isoprenoid precursor isopentenyl pyrophosphate, 1-deoxy-D-xylulose-5-phosphat
10 on of mevalonate 5-diphosphate (MDP) to form isopentenyl pyrophosphate, a ubiquitous precursor for is
11 thesis pathway responsible for production of isopentenyl-pyrophosphate, a short-chain phospholipid th
12 P), a microbial isoprenoid intermediate, and isopentenyl pyrophosphate, an endogenous isoprenoid inte
13 ylerythritol-phosphate (MEP) pathway forming isopentenyl pyrophosphate and a heterologous downstream
14 , pulsing of BZ-(C)-C(5)-OPP is inhibited by isopentenyl pyrophosphate and an inactive analog, sugges
16 mulation with prenyl pyrophosphate antigens (isopentenyl pyrophosphate and monomethyl phosphate).
17 madelta T cells have been shown to recognize isopentenyl pyrophosphate and related structures and hum
18 ed reactivity to the prenyl pyrophosphate Ag isopentenyl pyrophosphate and to its synthetic analogue
19 ood gamma delta T cells to the nonpeptide Ag isopentenyl pyrophosphate and to its synthetic analogue
20 s Ag-nonreactive TCR destroyed reactivity to isopentenyl pyrophosphate and to the mycobacterial super
21 nic lines showed a three-fold enhancement of isopentenyl pyrophosphate, and targeting AACPR, DBR2, an
23 inity of 1.1 muM, whereas the endogenous pAg isopentenyl pyrophosphate binds with an affinity of 627
24 mportant accessory cells that provide the Ag isopentenyl pyrophosphate, CD56(bright)CD11c(+) NK cells
25 of TRPA1, being inhibited by ruthenium red, isopentenyl pyrophosphate, HC-030031, A967079 or TRPA1 k
27 levels > or =30 microM profoundly inhibited isopentenyl pyrophosphate-induced release of the chemoki
29 zation of the two ubiquitous isoprene units, isopentenyl pyrophosphate (IPP) and dimethylallyl pyroph
32 amma-dimethylallyl pyrophosphate (DMAPP) and isopentenyl pyrophosphate (IPP) to all of the known terp
33 the recombinant truncated AaIPPI1 isomerized isopentenyl pyrophosphate (IPP) to dimethyl allyl pyroph
34 at catalyzes the reversible isomerization of isopentenyl pyrophosphate (IPP) to dimethylallyl pyropho
36 nsecutive condensation of eight molecules of isopentenyl pyrophosphate (IPP) with farnesyl pyrophosph
39 ol-4-phosphate pathway used by microbes, and isopentenyl pyrophosphate (IPP), an intermediate in the
40 encoding early steps in the biosynthesis of isopentenyl pyrophosphate (IPP), the precursor of all is
42 present only a subset of the phosphoantigen {isopentenyl pyrophosphate [IPP] and (E)-4-hydroxy-3-meth
45 onophosphate kinase superfamily, and between isopentenyl pyrophosphate isomerases and MutT pyrophosph
46 by nonpeptidic monoalkyl phosphates such as isopentenyl pyrophosphate leads to the up-regulation of
47 ay, catalyzes the successive condensation of isopentenyl pyrophosphate with dimethylallyl pyrophospha
48 ethylerythritol phosphate pathway to produce isopentenyl pyrophosphate with more favorable thermodyna
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