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1 PhyA in complex with myo-inositol hexa- and pentakisphosphate.
2 d levels of its precursor, diphosphoinositol pentakisphosphate.
3 ed dephosphorylation of inositol (1,3,4,5,6) pentakisphosphate.
7 rt a ciliary role for the inositol 1,3,4,5,6-pentakisphosphate 2-kinase (Ipk1) that generates inosito
9 polyphosphate multikinase (TbIPMK), inositol pentakisphosphate 2-kinase (TbIP5K) and inositol hexakis
12 sphate (IP6) by Ipk1, the inositol-1,3,4,5,6-pentakisphosphate 2-kinase, is required for Gle1-mediate
14 we observed increased expression of inositol pentakisphosphate 2-kinase, which was present in granule
15 ptides that increased (fragments of inositol pentakisphosphate 2-kinase, zona occludens 3, and FAT tu
17 inhibitor, 2-O-benzyl-myo-inositol 1,3,4,5,6-pentakisphosphate (2-O-Bn-InsP5), could affect PDK1/PLCg
18 pyrophosphate 5-diphosphoinositol 1,2,3,4,6-pentakisphosphate (5-InsP7) as follows: during a period
19 (IP6K1), which generates 5-diphosphoinositol pentakisphosphate (5-IP7), physiologically mediates nume
21 the beta phosphate from 5-diphosphoinositol pentakisphosphate (5PP-IP5), suggesting that increased l
23 akisphosphate (InsP(6)) to diphosphoinositol pentakisphosphate, a "high energy" candidate regulator o
25 ol pyrophosphates, such as diphosphoinositol-pentakisphosphate and bis-diphosphoinositol-tetrakisphos
26 trakisphosphate and subsequently to inositol pentakisphosphate and has also been described to functio
28 icient routes to 2-O-acyl inositol 1,3,4,5,6-pentakisphosphates and myo-inositol 1,3,4,5,6-pentakisph
29 ol pyrophosphates 5-InsP7 (diphosphoinositol pentakisphosphate) and 1,5-InsP8 (bis-diphosphoinositol
30 K(m) for ZmIPK1 using myo-inositol 1,3,4,5,6-pentakisphosphate as a substrate is 119 microm with a V(
31 on, our results implicate inositol 1,3,4,5,6-pentakisphosphate as an inhibitor of nonstop mRNA decay.
32 ion of inositol pyrophosphates from inositol pentakisphosphate but not inositol hexakisphosphate is i
33 s that synthesis of the majority of inositol pentakisphosphate, hexakisphosphate and pyrophosphate sp
34 in Rat-1 cells increased inositol 1,3,4,5,6-pentakisphosphate (I(1,3,4,5,6)P5) levels about 2-3-fold
35 and 6-phosphate groups of inositol 1,3,4,5,6-pentakisphosphate in IP binding and IPK1 activation.
36 rease the cellular levels of either inositol pentakisphosphate, inositol hexakisphosphate or other di
37 Specifically, cellular inositol 1,3,4,5,6-pentakisphosphate (InsP(5)) and inositol hexakisphosphat
38 tase (Minpp1) metabolizes inositol 1,3,4,5,6-pentakisphosphate (InsP(5)) and inositol hexakisphosphat
39 etrakisphosphate (InsP(4)) isomers, inositol pentakisphosphate (InsP(5)) and InsP(6), whereas its dep
40 st InsP(6) kinases were identified; inositol pentakisphosphate (InsP(5)) was phosphorylated to diphos
43 NA encoding the mammalian inositol 1,3,4,5,6-pentakisphosphate (InsP5) 2-kinase (2-kinase), the enzym
44 ase in the levels of both inositol 1,3,4,5,6-pentakisphosphate (InsP5) and inositol 1,2,3,4,5,6-hexak
48 ol pyrophosphates, such as diphosphoinositol pentakisphosphate (InsP7/IP7) and bis-diphosphoinositol
49 rophosphates, such as diphospho-myo-inositol pentakisphosphates (InsP7), are an important family of s
51 ylated inositols, such as inositol 1,3,4,5,6-pentakisphosphate (IP(5)) and inositol hexakisphosphate
53 the inositol pyrophosphate diphosphoinositol pentakisphosphate (IP(7)) physiologically phosphorylates
54 ol pyrophosphates, such as diphosphoinositol pentakisphosphate (IP(7)), are water-soluble inositol ph
55 or inositol tetrakisphosphate (IP4)/inositol pentakisphosphate (IP5) 2-kinase activity in phosphate s
56 kinase (IPMK) and its major product inositol pentakisphosphate (IP5) regulate a variety of cellular f
57 such as inositol tetrakisphosphate, inositol pentakisphosphate (IP5), and inositol hexakisphosphate (
60 2-kinase (IPK1) converts inositol 1,3,4,5,6-pentakisphosphate(IP5) to inositol hexakisphosphate (IP6
61 pyrophosphates, such as 5-diphosphoinositol pentakisphosphate (IP7), are generated by a family of in
62 he inositol pyrophosphate, diphosphoinositol pentakisphosphate (IP7), influences apoptotic cell death
64 the inositol pyrophosphate diphosphoinositol pentakisphosphate (IP7), which physiologically inhibits
67 cation from rat brain of a diphosphoinositol pentakisphosphate kinase (PPIP5K) that synthesizes (PP)2
70 he inositol pyrophosphate disphosphoinositol pentakisphosphate (PP-InsP(3)/InsP(7)) is formed in mamm
71 d two non-Nudix compounds: diphosphoinositol pentakisphosphate (PP-InsP(5)) and bis-diphosphoinositol
74 t inositol pyrophosphates (diphosphoinositol pentakisphosphate (PP-InsP5) and bisdiphosphoinositol te
76 was found to phosphorylate diphosphoinositol pentakisphosphate (PP-InsP5) to (PP)2-InsP4 (Vmax = 8.3
77 hexakisphosphate (IP6) and diphosphoinositol pentakisphosphate (PP-IP5 or IP7) kinase with similarity
80 n of another novel kinase, diphosphoinositol pentakisphosphate (PP-IP5) kinase, which uses PP-IP5 as
81 t the kinase required for inositol 1,3,4,5,6-pentakisphosphate production (Ipk2) is localized in the
82 he inositol pyrophosphate, diphosphoinositol pentakisphosphate, regulates p53 and protein kinase Akt
83 2-kinase) phosphorylates inositol 1,3,4,5,6-pentakisphosphate to inositol 1,2,3,4,5,6-hexakisphospha
85 addition, SopB hydrolyzes inositol 1,3,4,5,6 pentakisphosphate to yield inositol 1,4,5, 6-tetrakispho
86 the jasmonate co-receptor complex, inositol pentakisphosphate, which interacts with both COI1 and JA
87 entakisphosphates and myo-inositol 1,3,4,5,6-pentakisphosphate with biologically interesting and anti
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