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1 irmed in studies with Bacillus thuringiensis phosphatidylinositol-specific phospholipase C.
2 ce was confirmed by the release of apoB17 by phosphatidylinositol-specific phospholipase C.
3 face and could be released by treatment with phosphatidylinositol-specific phospholipase C.
4 the surface of cytotoxic T cells by glycosyl-phosphatidylinositol-specific phospholipase C.
5 an red blood cells and could be cleaved with phosphatidylinositol-specific phospholipase C.
6 engulfment modulated by cleavage of uPAR by phosphatidylinositol-specific phospholipase C.
7 -His catalytic dyad and for the mechanism of phosphatidylinositol-specific phospholipase C.
8 and subsite interactions of Bacillus cereus phosphatidylinositol-specific phospholipase C.
9 adenocarcinoma (NMU) cells and released with phosphatidylinositol-specific phospholipase C.
10 tes resisted release from cells treated with phosphatidylinositol-specific phospholipase C.
12 icles, RBC eluate preparations, and HDL with phosphatidylinositol-specific, phospholipase C, abrogate
13 rporation into DNA depends on an increase in phosphatidylinositol-specific phospholipase C activity a
14 is study, we designed and prepared a PI-PLC (Phosphatidylinositol-specific phospholipase C) activity-
15 They were firmly cell associated, resisted phosphatidylinositol-specific phospholipase C, aligned w
16 production by cultured microglial cells in a phosphatidylinositol-specific phospholipase C and DG lip
17 ion of metabotropic receptors coupled to the phosphatidylinositol-specific phospholipase C and diacyl
18 esistant to an enzyme that cleaves GPI-AChE (phosphatidylinositol-specific phospholipase C), and the
20 eversed-phase chromatography, treatment with phosphatidylinositol-specific phospholipase C, and chemi
21 hosphatidyl serine and phosphatidic acid), a phosphatidylinositol-specific phospholipase C, and full-
22 ositol 1-phosphate by Bacillus thuringiensis phosphatidylinositol-specific phospholipase C are activa
23 trolled events during the cell cycle involve phosphatidylinositol-specific phospholipase C as an effe
25 the membrane binding affinities of purified phosphatidylinositol-specific phospholipases C-beta 1 an
26 d not alter the membrane binding affinity of phosphatidylinositol-specific phospholipases C-beta 1, e
27 ns did not alter the membrane association of phosphatidylinositol-specific phospholipases C-beta 2 ev
28 as relatively insensitive to the presence of phosphatidylinositol-specific phospholipases C-beta s' m
30 ts provide constraints on how this bacterial phosphatidylinositol-specific phospholipase C binds to a
32 thuringiensis secretes the virulence factor phosphatidylinositol-specific phospholipase C (BtPI-PLC)
33 epatic lipase was released from the cells by phosphatidylinositol-specific phospholipase C but not by
34 ne anchor, evident from its insensitivity to phosphatidylinositol-specific phospholipase C but not ni
35 cytometry and was shown to be susceptible to phosphatidylinositol-specific phospholipase C cleavage.
37 trophoresis in conjunction with digestion by phosphatidylinositol-specific phospholipase C demonstrat
38 Treatment with phosphatidylinositol-specific phospholipase C demonstrat
39 Phosphatidylinositol-specific phospholipase C dissociate
40 botropic P2Y purinergic receptors coupled to phosphatidylinositol-specific phospholipase C does not i
41 s with either a cholesterol-binding agent or phosphatidylinositol-specific phospholipase C dramatical
42 tidylinositol anchored ephrin A ligands with phosphatidylinositol-specific phospholipase C enzyme tre
44 the phosphate ester accessible to attack by phosphatidylinositol-specific phospholipase C enzymes.
47 engineering the cation-pi box into secreted phosphatidylinositol-specific phospholipase C from Staph
50 phatidylinositol-anchored ART1 released with phosphatidylinositol-specific phospholipase C from trans
51 identification of an amino acid sequence in phosphatidylinositol-specific phospholipase C-gamma1 (PL
52 by protein kinase C acting via activation of phosphatidylinositol specific phospholipase C in the mac
53 perative multimeric enzymes even though this phosphatidylinositol-specific phospholipase C is a small
54 i) derive from the L. monocytogenes proteins phosphatidylinositol-specific phospholipase C, lecithina
56 almost abolished by treatment of cells with phosphatidylinositol-specific phospholipase C or anti-ap
59 The FR in L1210JF cells was sensitive to phosphatidylinositol specific phospholipase C (PI-PLC) i
60 ther virulence factors are phospholipases: a phosphatidylinositol-specific phospholipase C (PI-PLC [p
61 y was released from transformed NMU cells by phosphatidylinositol-specific phospholipase C (PI-PLC) a
70 ent phospholipids on the kinetic behavior of phosphatidylinositol-specific phospholipase C (PI-PLC) f
75 y, a 106-kDa APN, called AgAPN2, released by phosphatidylinositol-specific phospholipase C (PI-PLC) f
76 rystal structure of the W47A/W242A mutant of phosphatidylinositol-specific phospholipase C (PI-PLC) f
78 ropic proteins, such as the virulence factor phosphatidylinositol-specific phospholipase C (PI-PLC) f
82 ipase activity is inhibited by the selective phosphatidylinositol-specific phospholipase C (PI-PLC) i
83 It does not bind to DRG neurons treated with phosphatidylinositol-specific phospholipase C (PI-PLC) o
89 bstrate analog inhibitors of Bacillus cereus phosphatidylinositol-specific phospholipase C (PI-PLC) w
90 involved in generating secondary bile acids, phosphatidylinositol-specific phospholipase C (PI-PLC),
91 colonic mucosal phospholipase A2 (PLA2) and phosphatidylinositol-specific phospholipase C (PI-PLC),
92 activity of the peripheral membrane protein, phosphatidylinositol-specific phospholipase C (PI-PLC),
94 NgRs, evidenced by reversal of inhibition by phosphatidylinositol-specific phospholipase C (PI-PLC),
95 ria monocytogenes, listeriolysin O (LLO) and phosphatidylinositol-specific phospholipase C (PI-PLC),
97 either released from DRMs by treatment with phosphatidylinositol-specific phospholipase C (PI-PLC),
99 ns of secreted bacterial proteins, including phosphatidylinositol-specific phospholipase C (PI-PLC),
101 PrP-sen was also one of a small subset of phosphatidylinositol-specific phospholipase C (PI-PLC)-r
102 pore-forming toxin listeriolysin O (LLO) and phosphatidylinositol-specific phospholipase C (PI-PLC).
103 and from the sensitivity of the proteins to phosphatidylinositol-specific phospholipase C (PI-PLC).
104 n synthesized as water-soluble inhibitors of phosphatidylinositol-specific phospholipase C (PI-PLC).
105 has been used in a new, continuous assay for phosphatidylinositol-specific phospholipase C (PI-PLC).
106 ns from the surface of mammalian cells using phosphatidylinositol-specific phospholipase C (PI-PLC).
107 g from P2Y receptors to ERK is mediated by a phosphatidylinositol-specific phospholipase C (PI-PLC)/c
110 of geranylgeranylated beta gamma to activate phosphatidylinositol-specific phospholipase C (PIPLC) an
112 dominant form of TFPI released from cells by phosphatidylinositol-specific phospholipase C (PIPLC) tr
113 y was released from larval BBMVs prepared by phosphatidylinositol-specific phospholipase C (PIPLC) tr
114 CT-1 action on motoneurons was inhibited by phosphatidylinositol-specific phospholipase C (PIPLC), s
117 epsilon) is one of the newest members of the phosphatidylinositol-specific phospholipase C (PLC) fami
118 of a GTP-binding protein (G-protein)-coupled phosphatidylinositol-specific phospholipase C (PLC) in i
120 embrane stabilizer (sorbitol) or the loss of phosphatidylinositol-specific phospholipase C (PLC1) pro
122 )-anchored protein is also necessary because phosphatidylinositol-specific phospholipase C pretreatme
123 streptolysin O-permeabilized platelets with phosphatidylinositol-specific phospholipase C reduced Pt
124 Interestingly, neither membrane-anchored nor phosphatidylinositol-specific phospholipase C-released M
126 lpha-3 is anchored to the cell membrane by a phosphatidylinositol-specific phospholipase C-resistant
128 anchoring was confirmed by demonstrating the phosphatidylinositol-specific phospholipase C sensitivit
129 eptidase M was readily released by exogenous phosphatidylinositol-specific phospholipase C, showing i
130 itol 1,2-(cyclic) phosphate (cIP) binding to phosphatidylinositol-specific phospholipase C spin-label
131 52GA1 were released from the gut membrane by phosphatidylinositol specific-phospholipase C, suggestin
137 body binding studies and by the ability of a phosphatidylinositol-specific phospholipase C to release
140 dition of heparan sulfate, heparitinase, and phosphatidylinositol-specific phospholipase C to the med
142 e LPS-regulatory activity that was lost from phosphatidylinositol-specific phospholipase C-treated EV
143 t for NTN and GDNF signaling in SCG neurons; phosphatidylinositol-specific phospholipase C treatment
144 Membrane-bound prostasin can be released by phosphatidylinositol-specific phospholipase C treatment,
145 d NADase activity that was not releasable by phosphatidylinositol-specific phospholipase C treatment.
146 syltransferase solubilized from membranes by phosphatidylinositol-specific phospholipase C was separa
150 ral membrane protein, Bacillus thuringiensis phosphatidylinositol-specific phospholipase C, with both