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1 gulation by K-Ras and PI3-K but not RhoA and phosphatidylinositol 4-phosphate 5-kinase.
2 atidylinositol 4-kinase and a soluble type I phosphatidylinositol 4-phosphate 5-kinase.
3  regulates not only phospholipase D but also phosphatidylinositol 4-phosphate 5-kinase.
4 ding the downstream effectors Rho kinase and phosphatidylinositol-4-phosphate 5-kinase.
5 hate kinase type I gamma, the major neuronal phosphatidylinositol-4-phosphate 5-kinase.
6 o with a phosphatidylinositol 4-kinase and a phosphatidylinositol-4-phosphate 5-kinase.
7 1, was previously shown to encode a putative phosphatidylinositol-4-phosphate 5-kinase.
8 ve shown previously that the nuclear form of phosphatidylinositol-4-phosphate 5-kinase 1alpha (PIP5K)
9                                              Phosphatidylinositol-4-phosphate 5-kinase 1alpha (PIP5K1
10 and sequentially activated phospholipase D1, phosphatidylinositol-4-phosphate 5-kinase 1alpha, and NA
11 ns to PIP5K3 and COW1, which encode a type B phosphatidylinositol-4-phosphate 5-kinase 3 and a phosph
12                       Neither IP3 levels nor phosphatidylinositol 4-phosphate 5-kinase activity chang
13                                Additionally, phosphatidylinositol 4-phosphate 5-kinase activity in th
14 tidic acid, which potently stimulates type I phosphatidylinositol 4-phosphate 5-kinase activity, is g
15                                       Murine phosphatidylinositol 4-phosphate 5-kinase alpha (PI5KIal
16 lipid localization, as overexpression of the phosphatidylinositol 4-phosphate 5-kinase alpha [PtdIns(
17 s PIP2 turnover by recruiting and activating phosphatidylinositol 4-phosphate 5-kinases alpha (PIP5Ka
18                                              Phosphatidylinositol-4-phosphate 5-kinase-alpha (PIP5Kal
19 nds directly to Skittles (SKTL), a predicted phosphatidylinositol 4-phosphate 5-kinase, and genetic e
20 wn to be necessary for the export of Mss4, a phosphatidylinositol 4-phosphate 5-kinase, and required
21 pon activation by Sema3E, Plexin-D1 recruits phosphatidylinositol-4-phosphate 5-kinase, and its enzym
22 ns phosphatidylinositol transfer protein and phosphatidylinositol (4)-phosphate 5-kinase, as well as
23                Depletion of the human type I phosphatidylinositol 4-phosphate 5-kinase beta isoform (
24 endent on the C-terminal catalytic domain of phosphatidylinositol-4-phosphate 5-kinase but did not re
25                                              Phosphatidylinositol-4-phosphate-5-kinase cannot be dete
26 dentified the short splice variant of type I phosphatidylinositol 4-phosphate 5-kinase gamma (PIP5KIg
27 e IIIbeta and PKC; the increased activity of phosphatidylinositol 4-phosphate 5-kinase gamma was also
28                        Overexpression of the phosphatidylinositol 4-phosphate 5-kinase homolog MSS4 c
29 ncreased PIP(2) by transient expression of a phosphatidylinositol-4-phosphate-5-kinase (hPIP5KIbeta)
30 hough the alpha, beta, and gamma isoforms of phosphatidylinositol-4-phosphate-5-kinase I (PIP5KI) all
31 lear poly(A) polymerase that associates with phosphatidylinositol-4-phosphate 5-kinase Ialpha (PIPKIa
32 equired activation of p38, PKC isoforms, and phosphatidylinositol-4-phosphate 5-kinase Ialpha, a majo
33         Here, we demonstrated a role for the phosphatidylinositol 4-phosphate 5-kinase Igamma (PIPKIg
34 se (PI3-K), as well as RhoA and its effector phosphatidylinositol 4-phosphate 5-kinase increase ENaC
35 reasing PtdIns(4,5)P2 levels by coexpressing phosphatidylinositol-4-phosphate 5-kinase inhibited TRPV
36 I phosphoinositide 3-kinase, vps34p, and the phosphatidylinositol-4-phosphate 5-kinase, its3p, but do
37 ositol 4,5-biphosphate produced by activated phosphatidylinositol 4-phosphate 5-kinase may play a rol
38 fy a truncated form of the murine type Ibeta phosphatidylinositol 4-phosphate 5-kinase (mPIP5K-Ibeta)
39                                          The phosphatidylinositol-4-phosphate-5-kinase MSS4 was isola
40              We previously demonstrated that phosphatidylinositol-4-phosphate 5-kinase, one of the ef
41 cently, ion channel activity and activity of phosphatidylinositol 4-phosphate 5-kinase (PI(4)P 5-K).
42                                Three related phosphatidylinositol 4-phosphate 5-kinases (PI(4)P 5-kin
43     How the biosynthesis of PtdIns(4,5)P2 by phosphatidylinositol 4-phosphate 5-kinases (PI4P 5-kinas
44                Here, we targeted two related phosphatidylinositol 4-phosphate 5-kinases (PI4P 5-kinas
45                                              Phosphatidylinositol-4-phosphate-5-kinase (PI4P5K) has b
46 -derived endosomal compartment and activates phosphatidylinositol 4-phosphate 5-kinase (PIP 5-kinase)
47 emonstrated that Rac interacts with a type I phosphatidylinositol-4-phosphate 5-kinase (PIP 5-kinase)
48                Overexpression of type Ialpha phosphatidylinositol-4-phosphate 5-kinase [PIP(5)Kalpha]
49  intact myocardium, but not excised patches, phosphatidylinositol 4-phosphate 5-kinase (PIP5K) activi
50 dified Rho in its GTP-bound state stimulated phosphatidylinositol 4-phosphate 5-kinase (PIP5K) activi
51                                              Phosphatidylinositol 4-phosphate 5-kinase (PIP5K) cataly
52 Nexus (MORN) motif found in the lipid kinase-phosphatidylinositol 4-phosphate 5-kinase (PIP5K) family
53                                              Phosphatidylinositol 4-phosphate 5-kinase (PIP5K) gamma
54           We investigated the role of type I phosphatidylinositol 4-phosphate 5-kinase (PIP5K) gamma
55 R), a prototypical 7TMR, beta-arrestins bind phosphatidylinositol 4-phosphate 5-kinase (PIP5K) Ialpha
56 n of phosphatidylinositol 4-phosphate by the phosphatidylinositol 4-phosphate 5-kinase (PIP5K) to gen
57 isoforms of the main PIP2-generating enzyme, phosphatidylinositol 4-phosphate 5-kinase (PIP5K), play
58                            The regulation of phosphatidylinositol 4-phosphate 5-kinase (PIP5K), which
59 tor and a newly discovered 47-kDa isoform of phosphatidylinositol-4-phosphate 5-kinase (PIP5K), a mem
60 mmunity) now suggest that Btk also activates phosphatidylinositol-4-phosphate 5-kinase (PIP5K), there
61 sphosphate is mostly produced in the cell by phosphatidylinositol-4-phosphate 5-kinases (PIP5K) and h
62                                              Phosphatidylinositol-4-phosphate 5-kinases (PIP5K) synth
63 sm from an intergenic transcript between the phosphatidylinositol-4-phosphate 5-kinase (PIP5K1A) and
64 cruitment and activation of the lipid kinase phosphatidylinositol 4-phosphate 5-kinase (PIP5Kalpha).
65                                       Type I phosphatidylinositol-4-phosphate 5-kinase (PIP5KI) catal
66                            Three isoforms of phosphatidylinositol-4-phosphate 5-kinase (PIP5KIalpha,
67 rom plasma membrane-bound Arf GTPases to the phosphatidylinositol 4-phosphate 5-kinases (PIP5Ks) to g
68 rization and GLUT4 translocation, the type I phosphatidylinositol 4-phosphate 5-kinases (PIP5Ks) were
69                                              Phosphatidylinositol-4-phosphate 5-kinases (PIP5Ks) util
70 ic protein tyrosine kinases, associates with phosphatidylinositol-4-phosphate 5-kinases (PIP5Ks), the
71                 Here, we describe a role for phosphatidylinositol 4-phosphate 5-kinase (PIPK) Igammai
72 sitol 4,5-biphosphate (PIP2), synthesized by phosphatidylinositol 4-phosphate 5-kinase (PIPKI) enzyme
73  circuitry, is generated primarily by type I phosphatidylinositol 4-phosphate 5-kinases (PIPKIalpha,
74               Here, we show that type Igamma phosphatidylinositol 4-phosphate 5-kinase (PIPKIgamma) i
75              Here we report that type Igamma phosphatidylinositol-4-phosphate 5-kinase (PIPKIgamma) a
76 This PtdIns(4,5)P(2) dependence makes type I phosphatidylinositol 4-phosphate 5-kinases (PIPKIs) lync
77  cell migration, but the roles of the type I phosphatidylinositol-4-phosphate 5-kinases (PIPKIs), whi
78 on yeast zygotes and show by perturbation of phosphatidylinositol 4-phosphate 5-kinase that Mcp5 bind
79 e kinase type 1 gamma (PtdInsPKI gamma) is a phosphatidylinositol-4-phosphate 5-kinase that is expres
80 2) and is regulated by the associated Type I phosphatidylinositol-4-phosphate 5-kinase that synthesiz
81  producing PA, which is a known activator of phosphatidylinositol-4-phosphate 5 kinase, the enzyme re
82                          Here, we found that phosphatidylinositol 4-phosphate 5 kinase type 1C (PIP5K
83 dylinositol 4,5-bisphosphate (PIP2), and the phosphatidylinositol 4-phosphate 5-kinase type I (PIP5KI
84                                              Phosphatidylinositol 4-phosphate 5-kinase type I gamma (
85  generation in focal adhesions by the enzyme phosphatidylinositol 4-phosphate 5-kinase type Igamma ar
86                The interaction of talin with phosphatidylinositol(4) phosphate 5 kinase type I gamma
87                         Talin interacts with phosphatidylinositol-(4)-phosphate 5-kinase type Igamma,
88 ne enzyme responsible for PIP(2) production, phosphatidylinositol-4-phosphate 5-kinase type 1beta (PI
89 sphatidylinositol 4-kinase type II alpha and phosphatidylinositol-4-phosphate 5-kinase type I (PIP5KI
90 rough direct phosphorylation of FA-localized phosphatidylinositol-4-phosphate 5-kinase type-l gamma (

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