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1 C2 is a Na(+)-selective channel activated by phosphatidylinositol 3,5-bisphosphate.
2 s, phosphatidylinositol 3,4-bisphosphate and phosphatidylinositol 3,5-bisphosphate.
3 ylating phosphatidylinositol-3-phosphate and phosphatidylinositol-3,5-bisphosphate.
4 atidylinositol-5-phosphate (PI(5)P) or d-myo-phosphatidylinositol-3,5-bisphosphate.
5 PTase11 also hydrolyzes the 5-phosphate from phosphatidylinositol (3,5) bisphosphate.
6 onal marker) and its upstream molecule FIG4 (phosphatidylinositol (3,5)-bisphosphate 5-phosphatase) a
7 4 localized to lysosomes and associated with phosphatidylinositol (3,5)-bisphosphate, a key component
8 altered phosphoinositide levels [increase in phosphatidylinositol (3,5)-bisphosphate and decrease in
9 janins leads to increased cellular levels of phosphatidylinositol (3,5)-bisphosphate and phosphatidyl
10 rlay assay showed specific binding of SVB to phosphatidylinositol 3,5-bisphosphate and phosphatidylin
11 emonstrate that mVps24p selectively binds to phosphatidylinositol 3,5-bisphosphate and phosphatidylin
12 e data provide the first direct link between phosphatidylinositol 3,5-bisphosphate and the protein ma
13      This phase depends on the production of phosphatidylinositol-3,5-bisphosphate and the Fab1 compl
14     PIKfyve is a lipid kinase that generates phosphatidylinositol-3,5-bisphosphate and, directly or i
15 phatidylinositol 3-phosphate and its product phosphatidylinositol 3, 5-bisphosphate, and a WIPI-bindi
16 phatidylinositol 3-phosphate and synthesizes phosphatidylinositol 3,5-bisphosphate, and plays a criti
17 rylating phosphatidylinositol-3-phoshate and phosphatidylinositol-3,5-bisphosphate, and some members
18         It is accelerated by the PI(3)P- and phosphatidylinositol 3,5-bisphosphate-binding protein At
19 osphate in the identification of a mammalian phosphatidylinositol 3,5-bisphosphate-binding protein, m
20 erentially with maturing macropinosomes in a phosphatidylinositol 3,5-bisphosphate-dependent manner a
21 Kfyve modulates phagosome maturation through phosphatidylinositol-3,5-bisphosphate-dependent activati
22                                              Phosphatidylinositol 3,5-bisphosphate enables transport
23 n with synthetic biotinylated derivatives of phosphatidylinositol 3,5-bisphosphate in the identificat
24 inic acid adenine dinucleotide phosphate and phosphatidylinositol-3,5-bisphosphate, induce ion flux t
25                                              Phosphatidylinositol 3,5-bisphosphate is a membrane lipi
26 t synthesizes the endosomal phosphoinositide phosphatidylinositol-3,5-bisphosphate, is an essential r
27 hat the Vac14 protein, like Vac7p, regulates phosphatidylinositol 3,5-bisphosphate levels and possibl
28             FIG4 is a ubiquitously expressed phosphatidylinositol 3,5-bisphosphate phosphatase that r
29                                      The PPI phosphatidylinositol (3,5)-bisphosphate (PI(3,5)P2) is e
30              In light of this, the effect of phosphatidylinositol 3,5-bisphosphate (PI(3,5)P(2)) on v
31 hosphatidylinositol 3-phosphate (PI(3)P) and phosphatidylinositol 3,5-bisphosphate (PI(3,5)P(2)) regu
32                                              Phosphatidylinositol 3,5-bisphosphate (PI(3,5)P(2)), an
33                         The signaling lipid, phosphatidylinositol 3,5-bisphosphate (PI(3,5)P(2)), lik
34 e V(O) a-subunit ortholog Vph1 and the lipid phosphatidylinositol 3,5-bisphosphate (PI(3,5)P(2)).
35 tor cortactin as a direct binding partner of phosphatidylinositol 3,5-bisphosphate (PI(3,5)P2) and de
36                                              Phosphatidylinositol 3,5-bisphosphate (PI(3,5)P2) is a l
37                                              Phosphatidylinositol 3,5-bisphosphate (PI(3,5)P2) is the
38                                              Phosphatidylinositol 3,5-bisphosphate (PI(3,5)P2), a rec
39 he low-level endo-lysosomal signaling lipid, phosphatidylinositol 3,5-bisphosphate (PI(3,5)P2), is re
40 ity and assembly require the signaling lipid phosphatidylinositol 3,5-bisphosphate (PI(3,5)P2).
41 igand-gated channel that can be activated by phosphatidylinositol 3,5-bisphosphate [PI(3,5)P(2)] as w
42 that the rare late endosomal signaling lipid phosphatidylinositol 3,5-bisphosphate [PI(3,5)P(2)] dire
43 use defects in levels of the signaling lipid phosphatidylinositol 3,5-bisphosphate [PI(3,5)P(2)] lead
44                                              Phosphatidylinositol 3,5-bisphosphate [PI(3,5)P2] is a l
45 itive to the levels of the low abundant PIP, phosphatidylinositol 3,5-bisphosphate [PI(3,5)P2], becau
46  signaling lipids phosphatidic acid (PA) and phosphatidylinositol(3,5)bisphosphate [PI(3,5)P2].
47             We show that the signaling lipid phosphatidylinositol-3,5-bisphosphate [PI(3,5)P2] is req
48  other groups, claiming mammalian TPCs to be phosphatidylinositol-3,5-bisphosphate [PI(3,5)P2]-activa
49              VPA compromised the dynamics of phosphatidylinositol 3,5-bisphosphate (PI3,5P2) and grea
50 I), phosphatidylinositol-3-phosphate (PI3P), phosphatidylinositol-3,5-bisphosphate (PI3,5P2), and a r
51                                The mammalian phosphatidylinositol (3,5)-bisphosphate (PtdIns(3,5)P(2)
52 se (PIKfyve), a lipid kinase which generates phosphatidylinositol (3,5)-bisphosphate (PtdIns(3,5)P(2)
53 smotic stress induces a dramatic increase in phosphatidylinositol 3,5-bisphosphate (PtdIns 3,5-P(2))
54 rter GLUT4 onto the cell surface require the phosphatidylinositol 3,5-bisphosphate (PtdIns(3,5)P(2))
55                                          The phosphatidylinositol 3,5-bisphosphate (PtdIns(3,5)P(2))
56                                              Phosphatidylinositol 3,5-bisphosphate (PtdIns(3,5)P(2))
57                                              Phosphatidylinositol 3,5-bisphosphate (PtdIns(3,5)P2) he
58                                              Phosphatidylinositol 3,5-bisphosphate (PtdIns(3,5)P2) is
59  the budding yeast Saccharomyces cerevisiae, phosphatidylinositol 3,5-bisphosphate (PtdIns(3,5)P2) is
60                                              Phosphatidylinositol 3,5-bisphosphate (PtdIns(3,5)P2), a
61                                              Phosphatidylinositol 3,5-bisphosphate (PtdIns(3,5)P2), m
62                             Perturbations in phosphatidylinositol 3,5-bisphosphate (PtdIns(3,5)P2)-sy
63                                              Phosphatidylinositol 3,5-bisphosphate (PtdIns[3,5]P(2))
64                                              Phosphatidylinositol-3,5-bisphosphate (PtdIns(3,5)P(2))
65  analysis, the TRPML1 structure reveals that phosphatidylinositol-3,5-bisphosphate (PtdIns(3,5)P2) bi
66 smotically stressed, they rapidly synthesize phosphatidylinositol-3,5-bisphosphate (PtdIns(3,5)P2) by
67 the localization and regulation of mammalian phosphatidylinositol-3,5-bisphosphate (PtdIns(3,5)P2), a
68 -abundance and LEL-enriched signalling lipid phosphatidylinositol-3,5-bisphosphate (PtdIns(3,5)P2), w
69       Recently, two novel phosphoinositides, phosphatidylinositol-3,5-bisphosphate (PtdIns-3,5-P2) an
70 hatidylinositol 3-phosphate [PtdIns(3)P] and phosphatidylinositol 3,5-bisphosphate [PtdIns(3,5)P(2)]
71                                              Phosphatidylinositol-3,5-bisphosphate [PtdIns(3,5)P(2)]
72    PIKfyve is essential for the synthesis of phosphatidylinositol-3,5-bisphosphate [PtdIns(3,5)P2] an
73 wollen endosomal membranes is abrogated when phosphatidylinositol 3,5-bisphosphate synthesis is block
74 s involved in 5' messenger RNA decapping and phosphatidylinositol 3,5-bisphosphate synthesis were als
75 ive Vps34 drives certain pathways, including phosphatidylinositol-3,5-bisphosphate synthesis and retr
76               Tritiated arachidonic acid and phosphatidylinositol 3,5-bisphosphate were used to demon
77                                          For phosphatidylinositol 3,5-bisphosphate, where the two pho
78 ane association (dependent on interaction of phosphatidylinositol 3,5-bisphosphate with the N-termina