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1 Acetyl-L-alanyl-gamma-D-glutamyl-L-lysine]-3-acetoxymethyl-3-ceph em-carboxylic acid (compound 6), wa
2                           Furthermore, the 4-acetoxymethyl-3-methoxy-4-methyl-5-trimethylsilyl-2,5-cy
3                                        The 4-acetoxymethyl-4-alkyl-3-trimethylsilyl-2,5-cyclohexadien
4   BAPTA is delivered to the cytoplasm as the acetoxymethyl (AM) ester BAPTA/AM, but released AM group
5 s involving bulk loading of neurons with the acetoxymethyl (AM) ester version of Cal-590, combined tw
6          The study demonstrated that Calcein acetoxymethyl (AM) proved to be a suitable dye for detec
7       pHi was recorded fluorimetrically with acetoxymethyl (AM)-loaded carboxy-SNARF-1 at either 27 o
8  rabbit ventricular myocytes loaded with the acetoxymethyl ester (AM) form of carboxy-seminaphthorhod
9                     Myotubes loaded with the acetoxymethyl ester (AM) form of fluo-3 were imaged at r
10 of free cytosolic [Ca2+] ([Ca2+]c) using the acetoxymethyl ester (AM) form of indo-1 may be compromis
11 ing by cell-permeable Ca(2+) chelators [EGTA-acetoxymethyl ester (AM), 1, 2-bis(2-aminophenoxy)ethane
12 on flexible membranes and loaded with Fura-2 acetoxymethyl ester (AM).
13 rated that, like MDR1, SPGP effluxed calcein-acetoxymethyl ester (AM).
14 r esterase activity were analyzed by calcein-acetoxymethyl ester (AM)/ethidium homodimer assay.
15 + buffer, 2-aminophenol-N,N,O-triacetic acid acetoxymethyl ester (APTRA-AM, 20-40 mg/kg), on synaptic
16 inophenoxy)ethane-N,N,N',N'-tetraacetic acid-acetoxymethyl ester (BAPTA-AM) and completely eliminated
17 phenoxy)ethane-N, N, N', N'-tetraacetic acid-acetoxymethyl ester (BAPTA-AM) reduced cytosolic Ca(2+)
18 inophenoxy)ethane-N,N,N',N'-tetraacetic acid acetoxymethyl ester (BAPTA-AM), a Ca2+ chelator.
19 minophenoxy)ethane-N,N,N',N'-tetraacetate-AM acetoxymethyl ester (BAPTA-AM), cyclosporine, and inhibi
20 iniphenoxy)ethane-N,N,N',N'-tetraacetic acid acetoxymethyl ester (BAPTA-AM); and (4) after pretreatme
21 2-carboxyethyl)-5-(and-6)-carboxyfluorescein acetoxymethyl ester (BCECF-AM), that accumulates only in
22 in culture media containing 2 microM calcein-acetoxymethyl ester (calcein-AM) and 4 microM ethidium h
23 toma cells was evaluated with 4-hour calcein acetoxymethyl ester (calcein-AM) microcytotoxicity assay
24 o)-2'-O-methyladenosine-3',5'-monophosphate, acetoxymethyl ester (cpTOME) increased Socs3 expression
25            Ca2+ imaging studies using fura-2 acetoxymethyl ester (fura-2 AM) revealed that the increa
26 solic Ca2+ as measured by single-cell fura-2 acetoxymethyl ester (Fura-2) Ca2+-dependent fluorescence
27 y-2-naphthalenyl methyl phosphonic acid tris acetoxymethyl ester (HNMPA-(AM)(3)) inhibitor diminished
28                     Here, we show that NAADP acetoxymethyl ester (NAADP-AM), a cell-permeant NAADP an
29 pig cardiac myocytes were loaded with rhod-2-acetoxymethyl ester (rhod-2 AM), and [Ca2+]c was monitor
30 nt pH indicator carboxy seminaphtorhodafluor acetoxymethyl ester acetate, we measured pH(c) in the ce
31                In particular, Sulfidefluor-7 acetoxymethyl ester allows for direct, real-time visuali
32 nophenoxy)ethane-N,N,N', N'-tetraacetic acid acetoxymethyl ester also inhibited cytokine TNFalpha-ind
33 nophenoxy)ethane-N,N,N', N'-tetraacetic acid acetoxymethyl ester and EGTA acetoxymethyl ester and the
34 etraacetic acid acetoxymethyl ester and EGTA acetoxymethyl ester and the Ser/Thr phosphatase inhibito
35 , cell survival was quantified using calcein-acetoxymethyl ester compound and a fluorescent plate rea
36 d into arterioles by pre-incubation with the acetoxymethyl ester derivative.
37 th the sodium-binding bezofuran isophthalate acetoxymethyl ester fluorescence indicator.
38 )](i)), acini were incubated in fura-2 tetra-acetoxymethyl ester for 60 minutes at 22 degrees C, and
39 ent by buffering intracellular Ca2+ with the acetoxymethyl ester form of BAPTA (BAPTA AM).
40 ing by noradrenaline, OAG, PDBu, CPA and the acetoxymethyl ester form of BAPTA (BAPTA-AM) was markedl
41  of SOC activity evoked by either CPA or the acetoxymethyl ester form of BAPTA (BAPTA-AM).
42 ously cannot be attributed to the use of the acetoxymethyl ester form of fura-2 to report [Ca2+]i, an
43 of 2.2 micron in which the membrane permeant acetoxymethyl ester form of fura-2 was used.
44 ated from ferret or cat were loaded with the acetoxymethyl ester form of indo-1 (indo-1 AM) such that
45 ccomplished by incubating the cells with the acetoxymethyl ester forms (benz2 AM or BAPTA AM).
46 2-aminophenoxy)ethane-N,N,N',N'-tetraacetate/acetoxymethyl ester has similar effects to water immersi
47 inositol-1,4,5-trisphosphate (IP(3)) hexakis acetoxymethyl ester having an ortho-nitroveratryl photoc
48 O-methyladenosine 3',5'-cyclic monophosphate acetoxymethyl ester mimicked all butaprost effects.
49 erved when the fibers were preincubated with acetoxymethyl ester of 1,2-bis (2-amino-phenoxy) ethane
50 ngendorff perfused rabbit hearts loaded with acetoxymethyl ester of 1,2-bis(2-amino-5,6-difluoropheno
51  but not by calcium chelation with BAPTA-AM (acetoxymethyl ester of BAPTA) (75 microM for 30 min), su
52 xposure of the cone to the membrane-permeant acetoxymethyl ester of the Ca2+ chelator BAPTA.
53 inophenoxy)ethane-N,N,N',N'-tetraacetic acid/acetoxymethyl ester or thapsigargin.
54                Pretreatment with either EGTA acetoxymethyl ester or vitamin E resulted in a significa
55 inophenoxy)ethane-N,N,N',N'-tetraacetic acid acetoxymethyl ester produced a > 2-fold reduction in VP-
56 inophenoxy)ethane-N,N,N',N'-tetraacetic acid acetoxymethyl ester significantly decreased ET-1dependen
57 eceptor antagonists, was measured by calcein-acetoxymethyl ester staining after 3 days in culture.
58 vival rates of RGCs were measured by calcein-acetoxymethyl ester staining.
59 henoxy)ethane-N',N'-tetraacetic acid (BAPTA)-acetoxymethyl ester to buffer intracellular calcium resu
60 ith the fluorescent calcium indicator fura-2 acetoxymethyl ester to measure their intracellular Ca(2+
61 ith the fluorescent calcium indicator Fura-2 acetoxymethyl ester to measure their intracellular Ca2+
62       Application of membrane-permeant NAADP acetoxymethyl ester to PASMCs elicited a biphasic increa
63 yte-like U937 cells were labeled with fluo-3-acetoxymethyl ester to quantitate intracellular Ca2+ con
64 '-bis(2-carboxyethyl)-5,6-carboxyfluorescein-acetoxymethyl ester was used to quantitate intracellular
65 nophenoxy)ethane-N,N,N',N'-tetraacetic acid (acetoxymethyl ester) (BAPTA AM) did the opposite.
66 ethane-N,N, N',N'-tetraacetic acid tetrakis (acetoxymethyl ester) (BAPTA-AM) blocked both ERK and Ras
67 ethane-N,N,N',N'-tetra-acetic acid tetrakis (acetoxymethyl ester) (BAPTA-AM) or blockade of extracell
68 nophenoxy)ethane-N,N,N',N'-tetraacetic acid (acetoxymethyl ester) (BAPTA-AM) or the three specific ca
69 )ethane-N,N,N',N'-tetraacetic acid tetrakis (acetoxymethyl ester) (BAPTA-AM), an intracellular Ca(2+)
70 y)ethane-N,N,N',N'-tetraacetic acid tetrakis(acetoxymethyl ester) (BAPTA-AM), leads to a dramatic red
71 )ethane-N,N,N',N'-tetraacetic acid-tetrakis (acetoxymethyl ester) (BAPTA-AM).
72 simultaneous measurements of [Ca2+]i (fluo-3-acetoxymethyl ester) and membrane currents/action potent
73 y)ethane-N,N,N',N'-tetraacetic acid tetrakis(acetoxymethyl ester) and the phospholipase C inhibitor U
74 noxy)ethane-N,N,N',N'-tetraacetic acid tetra(acetoxymethyl ester) had no effect on the serotonin-indu
75 )ethane-N,N,N',N'-tetraacetic acid tetrakis (acetoxymethyl ester) inhibited the process by 50%.
76 y)ethane-N,N,N',N'-tetraacetic acid tetrakis(acetoxymethyl ester) or down-regulation of CaMKII by KN-
77 y)ethane-N,N,N',N'-tetraacetic acid tetrakis(acetoxymethyl ester) reduced cAMP levels in PC1-knock-ou
78 aminophenoxy)ethane-N,N,N,N-tetraacetic acid acetoxymethyl ester), an intracellular calcium chelator.
79 nophenoxy)ethane-N,N,N',N'-tetraacetic acid (acetoxymethyl ester), ROS scavengers, and the caspase in
80 inophenoxy)ethane-N,N,N',N'-tetraacetic acid acetoxymethyl ester), whereas activation of ERK was not
81 photo-activatable fluorophore, NPE-HCCC2/AM (acetoxymethyl ester); (ii) locally photolyzing a caged c
82  ethane-N,N,N',N'-tetraacetic acid tetrakis (acetoxymethyl ester)] treatments.
83 minophenoxy)ethaneN,N,N',N'-tetraacetic acid acetoxymethyl ester, an inhibitor of intracellular calci
84 inophenoxy)ethane-N,N,N',N'-tetraacetic acid-acetoxymethyl ester, an intracellular Ca(2+) chelator, b
85 inophenoxy)ethane-N,N,N',N'-tetraacetic acid acetoxymethyl ester, and by the guanyl cyclase inhibitor
86 oaded with the calcium indicator dye, fluo-3 acetoxymethyl ester, and fluorescence was measured by la
87 tion, cells were incubated with Fura 2 tetra acetoxymethyl ester, and intracellular [Ca(2+)] ([Ca(2+)
88 S indicators, Sulfidefluor-4, Sulfidefluor-5 acetoxymethyl ester, and Sulfidefluor-7 acetoxymethyl es
89  loaded with a calcium indicator dye, fluo-3 acetoxymethyl ester, and the fluorescence was measured b
90  smooth muscle cells were loaded with fluo-3 acetoxymethyl ester, and the fluorescence was recorded b
91 inophenoxy)ethane-N,N,N',N'-tetraacetic acid/acetoxymethyl ester, BAPTA/AM) fully inhibits intracellu
92 mitochondrial Ca(2+) uniporter, or with EGTA acetoxymethyl ester, but not with vitamin E, prevented t
93 inophenoxy)ethane-N,N,N',N'-tetraacetic acid acetoxymethyl ester, cyclopiazonic acid, and N,N,N',N'-t
94 red rat forebrain neurons loaded with indo-1 acetoxymethyl ester, KB-R7943 inhibited the reverse mode
95                                  Through its acetoxymethyl ester, Nmoc-DBHQ can be loaded into cells
96 lular calcium mobilization assay with fura-2 acetoxymethyl ester, peritoneal macrophages from wild-ty
97 inophenoxy)ethane-N,N,N',N'-tetraacetic acid-acetoxymethyl ester, removal of extracellular Ca(2+), th
98 inophenoxy)ethane-N,N,N',N'-tetraacetic acid-acetoxymethyl ester, the adenylate cyclase stimulant for
99 2-carboxyethyl)-5-(and-6)-carboxyfluorescein-acetoxymethyl ester, the initial rates of monocarboxylat
100 ponin or alpha-toxin the dye, loaded via its acetoxymethyl ester, was predominantly trapped in the sa
101 or-5 acetoxymethyl ester, and Sulfidefluor-7 acetoxymethyl ester, which offer the unique capability t
102                                    In fura-2-acetoxymethyl ester-loaded alveolar macrophages, intrace
103  Ca2+ concentration was equivalent in Fura-2 acetoxymethyl ester-loaded Q212L-alpha 16 cells compared
104 '-bis(2-carboxyethyl)-5(6)carboxyfluorescein-acetoxymethyl ester.
105 with the Ca(2+) fluorescent indicator Fura-2 acetoxymethyl ester.
106 with the fluorescent Ca(2+) indicator fluo-4 acetoxymethyl ester.
107 ]ethane-N,N,N',N'-tetraacetic acid tetrakis [acetoxymethyl ester]).
108 noxy)ethane-N,N,N',N'-tetraacetic acid tetra(acetoxymethyl) ester (BAPTA-AM) or inhibiting NO synthas
109 y)ethane-N,N,N',N'-tetraacetic acid tetrakis(acetoxymethyl) ester (BAPTA-AM) or the CaM antagonist W7
110 xy) ethane-N,N,N',N'-tetraacetic acid tetra (acetoxymethyl) ester (BAPTA-AM) reduced 5-HT release.
111 noxy)ethane-N,N,N',N'-tetraacetic acid tetra(acetoxymethyl) ester (BAPTA-AM) was added in some studie
112 noxy)ethane-N,N,N',N'-tetraacetic acid-tetra(acetoxymethyl) ester (BAPTA-AM), and PI3-K inhibitor (LY
113 nophenoxy)ethane-N,N,N',N'-tetraacetic acid-(acetoxymethyl) ester (BAPTA-AM), indicating that Ca(2+)
114 y)ethane-N,N,N',N'-tetraacetic acid tetrakis(acetoxymethyl) ester, 0.1 micromol/l), or by inhibiting
115 s (o-aminophenoxy) ethane-tretraacetic acid (acetoxymethyl) ester, and dantrolene, did not alter bort
116 oxy)ethane-N,N,N', N'-tetraacetic acid/tetra(acetoxymethyl) ester, protected the cells against injury
117 yl-myo-inositol 1,3, 4-trisphosphate-hexakis(acetoxymethyl) ester.
118 nophenoxy)ethane-N,N,N',N'-tetraacetic acid (acetoxymethyl) ester.
119 phenoxy)ethane-N,N,N,N',N'-tetraacetic acid (acetoxymethyl)ester (BAPTA-AM) abolished aggregation ind
120 noxy)ethane-N,N,N',N'-tetraacetic acid tetra(acetoxymethyl)ester (BAPTA-AM).
121 o-inositol 3,4,5,6-tetrakisphosphate octakis(acetoxymethyl)ester (Bt(2)Ins (3,4,5,6)P(4)/AM).
122 -8-bis-(carboxymethyl)-aminoquinoline tetra-(acetoxymethyl)ester (Quin/AM), a calcium chelator, or wi
123 nophenoxy)ethane-N,N,N',N'-tetraacetic acid (acetoxymethyl)ester.
124 enoxy)ethane-N,N,N',N'tetraacetic acid tetra(acetoxymethyl)ester.
125 nyl)-ethane-N,N,N',N'-tetraacetic acid tetra(acetoxymethyl)-ester, a chelator of intracellular Ca2+.
126 oxy)ethane-N,N,N',N'-tetraacetic acid, tetra(acetoxymethyl)-ester, a membrane-permeable calcium chela
127 xy)-ethane-N,N,N',N'-tetraacetic acid tetra-(acetoxymethyl)-ester.
128 BAPTA) or pretreatment of oocytes with BAPTA-acetoxymethyl-ester (BAPTA-AM) nearly completely prevent
129 ',7'-bis-2-carboxyethyl-5-carboxyfluorescein-acetoxymethyl-ester (BCECF).
130                                          The acetoxymethyl esterified sensor variant was readily take
131 amps) to validate the selectivity with which acetoxymethyl esters (AM-esters) of cAMP analogs prefere
132 he isolated fiber cells were loaded with the acetoxymethyl esters of Fluo-3 or Calcium Green-2, or wi
133 -C8-PIP3/AM and di-C12-PIP3/AM, the heptakis(acetoxymethyl) esters of dioctanoyl- and dilauroylphosph
134 , plasma membrane integrity based on calcein-acetoxymethyl fluorescence was significantly greater at
135 re tagged by uptake of one of the following: acetoxymethyl of 2',7'-bis-(2-carboxyethyl)-5-(and 6)-ca
136 oacridine conjugate of a silyl-protected bis(acetoxymethyl)phenol (bisQMP) was synthesized and evalua
137 inophenoxy)ethane-N,N,N',N'-tetraacetic acid-acetoxymethyl) prevented the CT-induced disappearance of
138 etate derivative, 5-[(acetylamino)methyl]-2-(acetoxymethyl)pyridine (37).
139                                     While 3'-acetoxymethyl-substituted cephalosporins are readily ava
140       Viable cells were labeled with calcein acetoxymethyl, visualized using fluorescent microscopy,
141 present series is compound 8b [(1S,3R,6S)-2-(acetoxymethyl)-(Z)-9-(3, 4-dichlorophenylmethylene)-7-az

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