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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
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
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
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
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
31 hosphatidylinositol 3-phosphate (PI(3)P) and phosphatidylinositol 3,5-bisphosphate (PI(3,5)P(2)) regu
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
39 he low-level endo-lysosomal signaling lipid, phosphatidylinositol 3,5-bisphosphate (PI(3,5)P2), is re
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
45 itive to the levels of the low abundant PIP, phosphatidylinositol 3,5-bisphosphate [PI(3,5)P2], becau
48 other groups, claiming mammalian TPCs to be phosphatidylinositol-3,5-bisphosphate [PI(3,5)P2]-activa
50 I), phosphatidylinositol-3-phosphate (PI3P), phosphatidylinositol-3,5-bisphosphate (PI3,5P2), and a r
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))
59 the budding yeast Saccharomyces cerevisiae, phosphatidylinositol 3,5-bisphosphate (PtdIns(3,5)P2) is
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
70 hatidylinositol 3-phosphate [PtdIns(3)P] and 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
78 ane association (dependent on interaction of phosphatidylinositol 3,5-bisphosphate with the N-termina