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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 tes resisted release from cells treated with phosphatidylinositol-specific phospholipase C.
8 -His catalytic dyad and for the mechanism of phosphatidylinositol-specific phospholipase C.
9 and subsite interactions of Bacillus cereus phosphatidylinositol-specific phospholipase C.
10 adenocarcinoma (NMU) cells and released 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 They were firmly cell associated, resisted phosphatidylinositol-specific phospholipase C, aligned w
15 production by cultured microglial cells in a phosphatidylinositol-specific phospholipase C and DG lip
16 ion of metabotropic receptors coupled to the phosphatidylinositol-specific phospholipase C and diacyl
17 esistant to an enzyme that cleaves GPI-AChE (phosphatidylinositol-specific phospholipase C), and the
19 eversed-phase chromatography, treatment with phosphatidylinositol-specific phospholipase C, and chemi
20 hosphatidyl serine and phosphatidic acid), a phosphatidylinositol-specific phospholipase C, and full-
21 ositol 1-phosphate by Bacillus thuringiensis phosphatidylinositol-specific phospholipase C are activa
22 trolled events during the cell cycle involve phosphatidylinositol-specific phospholipase C as an effe
24 the membrane binding affinities of purified phosphatidylinositol-specific phospholipases C-beta 1 an
25 d not alter the membrane binding affinity of phosphatidylinositol-specific phospholipases C-beta 1, e
26 ns did not alter the membrane association of phosphatidylinositol-specific phospholipases C-beta 2 ev
27 as relatively insensitive to the presence of phosphatidylinositol-specific phospholipases C-beta s' m
29 ts provide constraints on how this bacterial phosphatidylinositol-specific phospholipase C binds to a
31 thuringiensis secretes the virulence factor phosphatidylinositol-specific phospholipase C (BtPI-PLC)
32 epatic lipase was released from the cells by phosphatidylinositol-specific phospholipase C but not by
33 ne anchor, evident from its insensitivity to phosphatidylinositol-specific phospholipase C but not ni
34 cytometry and was shown to be susceptible to phosphatidylinositol-specific phospholipase C cleavage.
36 trophoresis in conjunction with digestion by phosphatidylinositol-specific phospholipase C demonstrat
37 Treatment with phosphatidylinositol-specific phospholipase C demonstrat
38 botropic P2Y purinergic receptors coupled to phosphatidylinositol-specific phospholipase C does not i
39 s with either a cholesterol-binding agent or phosphatidylinositol-specific phospholipase C dramatical
40 tidylinositol anchored ephrin A ligands with phosphatidylinositol-specific phospholipase C enzyme tre
42 the phosphate ester accessible to attack by phosphatidylinositol-specific phospholipase C enzymes.
45 engineering the cation-pi box into secreted phosphatidylinositol-specific phospholipase C from Staph
48 phatidylinositol-anchored ART1 released with phosphatidylinositol-specific phospholipase C from trans
49 identification of an amino acid sequence in phosphatidylinositol-specific phospholipase C-gamma1 (PL
50 by protein kinase C acting via activation of phosphatidylinositol specific phospholipase C in the mac
51 perative multimeric enzymes even though this phosphatidylinositol-specific phospholipase C is a small
52 i) derive from the L. monocytogenes proteins phosphatidylinositol-specific phospholipase C, lecithina
54 almost abolished by treatment of cells with phosphatidylinositol-specific phospholipase C or anti-ap
57 The FR in L1210JF cells was sensitive to phosphatidylinositol specific phospholipase C (PI-PLC) i
58 ther virulence factors are phospholipases: a phosphatidylinositol-specific phospholipase C (PI-PLC [p
59 y was released from transformed NMU cells by phosphatidylinositol-specific phospholipase C (PI-PLC) a
68 ent phospholipids on the kinetic behavior of phosphatidylinositol-specific phospholipase C (PI-PLC) f
73 y, a 106-kDa APN, called AgAPN2, released by phosphatidylinositol-specific phospholipase C (PI-PLC) f
74 rystal structure of the W47A/W242A mutant of phosphatidylinositol-specific phospholipase C (PI-PLC) f
76 ropic proteins, such as the virulence factor phosphatidylinositol-specific phospholipase C (PI-PLC) f
80 ipase activity is inhibited by the selective phosphatidylinositol-specific phospholipase C (PI-PLC) i
81 It does not bind to DRG neurons treated with phosphatidylinositol-specific phospholipase C (PI-PLC) o
87 bstrate analog inhibitors of Bacillus cereus phosphatidylinositol-specific phospholipase C (PI-PLC) w
88 involved in generating secondary bile acids, phosphatidylinositol-specific phospholipase C (PI-PLC),
89 colonic mucosal phospholipase A2 (PLA2) and phosphatidylinositol-specific phospholipase C (PI-PLC),
90 activity of the peripheral membrane protein, phosphatidylinositol-specific phospholipase C (PI-PLC),
92 NgRs, evidenced by reversal of inhibition by phosphatidylinositol-specific phospholipase C (PI-PLC),
93 ria monocytogenes, listeriolysin O (LLO) and phosphatidylinositol-specific phospholipase C (PI-PLC),
95 either released from DRMs by treatment with phosphatidylinositol-specific phospholipase C (PI-PLC),
97 ns of secreted bacterial proteins, including phosphatidylinositol-specific phospholipase C (PI-PLC),
99 PrP-sen was also one of a small subset of phosphatidylinositol-specific phospholipase C (PI-PLC)-r
100 and from the sensitivity of the proteins to phosphatidylinositol-specific phospholipase C (PI-PLC).
101 n synthesized as water-soluble inhibitors of phosphatidylinositol-specific phospholipase C (PI-PLC).
102 has been used in a new, continuous assay for phosphatidylinositol-specific phospholipase C (PI-PLC).
103 ns from the surface of mammalian cells using phosphatidylinositol-specific phospholipase C (PI-PLC).
104 g from P2Y receptors to ERK is mediated by a phosphatidylinositol-specific phospholipase C (PI-PLC)/c
107 of geranylgeranylated beta gamma to activate phosphatidylinositol-specific phospholipase C (PIPLC) an
109 dominant form of TFPI released from cells by phosphatidylinositol-specific phospholipase C (PIPLC) tr
110 y was released from larval BBMVs prepared by phosphatidylinositol-specific phospholipase C (PIPLC) tr
111 CT-1 action on motoneurons was inhibited by phosphatidylinositol-specific phospholipase C (PIPLC), s
114 epsilon) is one of the newest members of the phosphatidylinositol-specific phospholipase C (PLC) fami
115 of a GTP-binding protein (G-protein)-coupled phosphatidylinositol-specific phospholipase C (PLC) in i
117 embrane stabilizer (sorbitol) or the loss of phosphatidylinositol-specific phospholipase C (PLC1) pro
119 )-anchored protein is also necessary because phosphatidylinositol-specific phospholipase C pretreatme
120 streptolysin O-permeabilized platelets with phosphatidylinositol-specific phospholipase C reduced Pt
121 Interestingly, neither membrane-anchored nor phosphatidylinositol-specific phospholipase C-released M
123 lpha-3 is anchored to the cell membrane by a phosphatidylinositol-specific phospholipase C-resistant
125 anchoring was confirmed by demonstrating the phosphatidylinositol-specific phospholipase C sensitivit
126 eptidase M was readily released by exogenous phosphatidylinositol-specific phospholipase C, showing i
127 itol 1,2-(cyclic) phosphate (cIP) binding to phosphatidylinositol-specific phospholipase C spin-label
128 52GA1 were released from the gut membrane by phosphatidylinositol specific-phospholipase C, suggestin
134 body binding studies and by the ability of a phosphatidylinositol-specific phospholipase C to release
137 dition of heparan sulfate, heparitinase, and phosphatidylinositol-specific phospholipase C to the med
139 t for NTN and GDNF signaling in SCG neurons; phosphatidylinositol-specific phospholipase C treatment
140 Membrane-bound prostasin can be released by phosphatidylinositol-specific phospholipase C treatment,
141 d NADase activity that was not releasable by phosphatidylinositol-specific phospholipase C treatment.
142 syltransferase solubilized from membranes by phosphatidylinositol-specific phospholipase C was separa
145 ral membrane protein, Bacillus thuringiensis phosphatidylinositol-specific phospholipase C, with both
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