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1 cluding phosphatidylinositol 3-phosphate and phosphatidylinositol 3,4-bisphosphate).
2 dylinositol 3,4, 5-trisphosphate (PIP3) into phosphatidylinositol 3,4-bisphosphate.
3 phosphatidylinositol 3,4, 5-trisphosphate to phosphatidylinositol 3,4-bisphosphate.
4 -3-position phosphates as substrates to form phosphatidylinositol 3,4-bisphosphate.
5 phosphorylation of PI(3,4,5)P(3) to generate phosphatidylinositol-(3,4)-bisphosphate.
6 hibition of 4-phosphatase is involved in the phosphatidylinositol 3, 4-bisphosphate accumulation in t
7 t not carbachol, rapidly increased levels of phosphatidylinositol (3,4)-bisphosphate and phosphatidyl
8 activity results in the reduced synthesis of phosphatidylinositol 3,4 bisphosphate and phosphatidylin
9 the p47(phox) PX domain is triggered by both phosphatidylinositol 3,4-bisphosphate and phosphatidic a
10 the 3-phosphate-containing inositol lipids, phosphatidylinositol 3,4-bisphosphate and phosphatidylin
11 d with either gene showed elevated levels of phosphatidylinositol 3,4-bisphosphate and phosphatidylin
12 lated products of the soluble derivatives of phosphatidylinositol 3,4-bisphosphate and phosphatidylin
13 as two lipid binding sites, one specific for phosphatidylinositol 3,4-bisphosphate and the other with
14 hosphatidylinositol 3,4, 5-trisphosphate and phosphatidylinositol 3,4-bisphosphate and, by doing so,
15 E activity was similarly stimulated by d-myo-phosphatidylinositol-3,4-bisphosphate and d-myo-phosphat
16 tivity, we determined that whereas levels of phosphatidylinositol-3,4-bisphosphate and phosphatidylin
17 l-4,5-bisphosphate (PIns-4,5-P2), its isomer phosphatidylinositol-3,4-bisphosphate and phosphatidylin
18 affinity for this phosphatidylinositol over phosphatidylinositol-3,4-bisphosphate and the -3,4,5-tri
19 nit type 2a), its lipid product PI(3,4)P(2) (phosphatidylinositol 3,4-bisphosphate), and the PI(3,4)P
21 itol(3,4,5)-triphosphate and accumulation of phosphatidylinositol(3,4)-bisphosphate at invadopodia is
22 tive to dynamic changes in PI(3,4,5)P(3) and phosphatidylinositol-(3,4)-bisphosphate both in vitro an
23 d by PtdIns(3,4,5)P(3) (IC(50) = 150 nm) and phosphatidylinositol 3,4-bisphosphate but not by their n
24 ellular phosphatidylinositol 3-phosphate and phosphatidylinositol 3, 4-bisphosphate, by plasma membra
25 nositol 4-phosphate was a weak activator and phosphatidylinositol 3,4-bisphosphate did not activate G
27 at phosphatidylinositol 4,5-bisphosphate and phosphatidylinositol 3, 4-bisphosphate in pure micelles
28 r, calpeptin, suppressed the accumulation of phosphatidylinositol 3, 4-bisphosphate in thrombin-stimu
29 to phosphatidylinositol 3,5-bisphosphate and phosphatidylinositol 3,4-bisphosphate in preference to o
31 he hydrolysis of the 4-position phosphate of phosphatidylinositol 3,4-bisphosphate, inositol 1,3,4-tr
32 itol 3,4,5-trisphosphate and conversion into phosphatidylinositol 3,4-bisphosphate occur in SHIP-defi
33 gen activation do not significantly increase phosphatidylinositol-3,4-bisphosphate or phosphatidylino
34 ignaling roles of its minor lipid messenger, phosphatidylinositol (3,4)-bisphosphate (PI(3,4)P(2)), a
35 d phagocytosis, the product of its activity, phosphatidylinositol 3,4 bisphosphate (PI(3,4)P(2)), has
36 tidylinositol 3,4,5-trisphosphate (PIP3) and phosphatidylinositol 3,4-bisphosphate (PI 3,4-P2) have b
38 levels of PI(3,4,5)P(3) and higher levels of phosphatidylinositol 3,4-bisphosphate (PI(3,4)P(2)) as w
39 inositol 3,4,5-trisphosphate (PIP(3)) and/or phosphatidylinositol 3,4-bisphosphate (PI(3,4)P(2)) with
41 linositol 4,5-bisphosphate (PI(4,5)P(2)) and phosphatidylinositol 3,4-bisphosphate (PI(3,4)P(2)).
42 dylinositol 4,5-bisphosphate (PI(4,5)P2) and phosphatidylinositol 3,4-bisphosphate (PI(3,4)P2) in vit
43 ositol 3,4,5-trisphosphate (PI(3,4,5)P3) and phosphatidylinositol 3,4-bisphosphate (PI(3,4)P2), sugge
46 3-kinase (PI3K) activation and synthesis of phosphatidylinositol-3,4-bisphosphate (PI-3,4-P2) and ph
48 he peckstrin homology (PH) domain in Lpd and phosphatidylinositol (3,4)-bisphosphate [PI(3,4)P2] on t
51 to phosphatidylinositol 4,5-bisphosphate and phosphatidylinositol 3,4-bisphosphate [PI(3,4)P(2)], res
52 atidylinositol 3,4,5-triphosphate (PIP3) and phosphatidylinositol 3,4-bisphosphate [PI(3,4)P2] regula
53 itol-3,4,5-trisphosphate [PI(3,4,5)P(3)] and phosphatidylinositol-3,4-bisphosphate [PI(3,4)P(2)] via
54 phosphatidylinositol-3,4,5-trisphosphate and phosphatidylinositol-3,4-bisphosphate [PI(3,4)P2] and co
55 In these vesicles, PI3K-C2gamma produces a phosphatidylinositol-3,4-bisphosphate pool specifically
56 plasma membrane, intracellular clathrin and phosphatidylinositol-3,4-bisphosphate predict the excita
57 rominent at the leading edges of cells where phosphatidylinositol-3,4-bisphosphate-produced by the de
58 phosphatidylinositol 3,4,5-trisphosphate and phosphatidylinositol 3,4-bisphosphate promote cell survi
60 O(2) caused almost exclusive accumulation of phosphatidylinositol 3,4-bisphosphate (PtdIns(3, 4)P(2))
61 3,4,5-trisphosphate (PtdIns(3,4,5)P(3)) and phosphatidylinositol 3,4-bisphosphate (PtdIns(3,4)P(2)),
63 nositol 4,5-bisphosphate (PtdIns(4,5)P2) and phosphatidylinositol 3,4-bisphosphate (PtdIns(3,4)P2) wi
64 hate (PtdIns(3,4,5)P3) and a small amount of phosphatidylinositol 3,4-bisphosphate (PtdIns(3,4)P2).
65 ome through lipid-mediated interactions with phosphatidylinositol-3,4-bisphosphate (PtdIns(3,4)P(2))
66 PI3K-C2beta, we find that generation of the phosphatidylinositol-3,4-bisphosphate (PtdIns(3,4)P(2))
67 that bind to the major products of PI 3'-K: phosphatidylinositol-3,4-bisphosphate (PtdIns-3,4-P(2))
68 ty was found to correlate with the amount of phosphatidylinositol-3,4-bisphosphate (PtdIns-3,4-P2) in
69 nd D-4 phosphoinositides examined, including phosphatidylinositol 3, 4-bisphosphate [PtdIns(3,4)P2],
70 rent specificities: one preferentially binds phosphatidylinositol 3,4-bisphosphate [PtdIns(3,4)P(2)]
71 be 1.1 microM, 5.7 microM, and 11 microM for phosphatidylinositol 3,4-bisphosphate [PtdIns(3,4)P2], p
72 the TrioN-PH domain does not detectably bind phosphatidylinositol 3,4-bisphosphate, PtdIns(3,4)P(2),
73 tol 3,4,5-trisphosphate (Ptdlns(3,4,5)P3) or phosphatidylinositol 3,4-bisphosphate (Ptdlns(3,4)P2).
74 In addition, type I PIP5Ks phosphorylate phosphatidylinositol 3, 4-bisphosphate to phosphatidylin
75 phosphatidylinositol 3,4,5-trisphosphate and phosphatidylinositol 3,4-bisphosphate, to the pleckstrin
77 he hydrolysis of the 4-position phosphate of phosphatidylinositol 3,4-bisphosphate, was shown to be a