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1 ing stochastic single-nanoparticle collision amperometry.
2  efflux comparable with hDAT was detected by amperometry.
3 ely to act as the major detected compound in amperometry.
4 by measurements of [(3)H]dopamine efflux and amperometry.
5 sing a diamond microelectrode and continuous amperometry.
6  on the ITO electrode beneath the cell using amperometry.
7 amphetamine-induced DA efflux as measured by amperometry.
8  or 3.2 x 10(10) viral particles/mL with RDE amperometry.
9  ventral midbrain neurons using carbon fiber amperometry.
10 ll capacitance measurements and carbon fibre amperometry.
11  observations of insulin release detected by amperometry.
12 m chromaffin cells using cell-attached patch amperometry.
13 olamine measured with cyclic voltammetry and amperometry.
14 n and directly detected by integrated pulsed amperometry.
15 do-1 microfluorometry and constant potential amperometry.
16 gated by normal-pulse voltammetry and pulsed amperometry.
17 capacitance, FM1-43 fluorescence imaging and amperometry.
18 ntaneous and evoked quantal release of DA by amperometry.
19 stepwise increases in current as observed by amperometry.
20 nts of exocytosis obtained simultaneously by amperometry.
21 es and small vesicles, has been studied with amperometry.
22 ous indo-1 photometry and constant potential amperometry.
23 hed dye, and catecholamines were detected by amperometry.
24 elease of vesicular contents was followed by amperometry.
25 ochemical techniques: cyclic voltammetry and amperometry.
26 rent spikes by the electrochemical method of amperometry.
27 ule release with carbon-fiber microelectrode amperometry.
28 ric oxide (NO) production was assessed using amperometry.
29 icosities in the Drosophila larval system by amperometry.
30 erface was studied by cyclic voltammetry and amperometry.
31 b sulfide were achieved using flow injection amperometry.
32 her cyclic voltammetry or constant potential amperometry.
33  were studied by cyclic voltammetry (CV) and amperometry.
34 ipally with disk carbon fiber microelectrode amperometry.
35 ermined from direct glucose injection during amperometry.
36  conductivity, which was monitored by pulsed amperometry.
37 -noise ratio = 3) using controlled potential amperometry.
38 lection fluorescence microscopy (pTIRFM) and amperometry.
39 nhanced neurotransmitter release measured by amperometry.
40 ddress this question, we used in vivo oxygen amperometry, a proxy for blood oxygen level-dependent (B
41                                       Pulsed amperometry allowed a direct detection of the carbohydra
42  detected with rotating disk electrode (RDE) amperometry and an interdigitated array (IDA) electrode.
43  obtained with amperometry may indicate that amperometry and capacitance detect the fusion of differe
44 h-clamped PC12 cells was analyzed using both amperometry and capacitance measurements.
45 holamine secretion was measured by oxidative amperometry and cell membrane turnover was measured by v
46 is mutant were characterized by carbon fiber amperometry and cell-attached patch capacitance measurem
47 1E mutants were investigated by carbon fiber amperometry and cell-attached patch capacitance measurem
48                                         Here amperometry and conductance measurements were performed
49  and it demonstrates that the combination of amperometry and constant-impedance SECM has the potentia
50                               Flow injection amperometry and cyclic voltammetry were used to assess a
51 imilar when measured with constant potential amperometry and cyclic voltammetry.
52 ons for stimulated release of dopamine using amperometry and cyclic voltammetry.
53 rflow in striatal slices by using continuous amperometry and cyclic voltammetry.
54         The results from cyclic voltammetry, amperometry and electrochemical impedance spectroscopy d
55 lytical methods (potentiometry, voltammetry, amperometry and electrochemical impedance spectroscopy)
56                                         Both amperometry and electron micrograph data were analyzed b
57 2 cells using alternately constant-potential amperometry and fast-scan cyclic voltammetry (FSCV).
58 anges were compared using constant potential amperometry and fast-scan cyclic voltammetry.
59  edge findings and technological advances in amperometry and fast-scan cyclic voltammetry.
60 ent bonding and detection techniques such as amperometry and fluorescence measurements are discussed
61                                        Using amperometry and FMRFamide tagging, I simultaneously meas
62  crosstalk between electrodes when comparing amperometry and FSCV.
63 rsors, and metabolites, were evaluated using amperometry and high performance liquid chromatography w
64 ydrogen peroxide (H(2)O(2)) was evaluated by amperometry and the so-made amperometric biosensor was a
65                                              Amperometry and transmission electron microscopy have be
66                                              Amperometry and transmission electron microscopy have be
67 ypical millimolar concentrations employed in amperometry and voltammetry.
68 s for glucose oxidation using flow injection amperometry and voltammetry.
69 to perform electrochemical measurements like amperometry and voltammetry.
70 studied by confocal fluorescence microscopy, amperometry, and cell-attached capacitance measurements.
71                High-speed chronoamperometry, amperometry, and differential pulse voltammetry were use
72                         This was detected by amperometry, and it was found to be accompanied by Ca2+
73 ating ion-selective electrodes, carbon fiber amperometry, and magnetic resonance imaging, we monitore
74 nd glucose, respectively, using voltammetry, amperometry, and potentiometry.
75 racterized using finite element simulations, amperometry, and Raman experiments.
76 differentiated PC12 cells using carbon-fiber amperometry, and relative diameters of individual vesicl
77  secretion from single cells was detected by amperometry as a series of current spikes corresponding
78  from chromaffin cells by constant potential amperometry as well as fast-scan cyclic voltammetry.
79 were evaluated by dynamic constant potential amperometry at 1.3V under non-buffered conditions.
80 re determined by cyclic voltammetry (CV) and amperometry at a custom thin-layer cell (TLC) detector.
81                                              Amperometry at a rotating disk electrode at 0 V gave sen
82                         GluA was measured by amperometry at a working potential of 0.6 V vs Ag/AgCl.
83                                              Amperometry at the carbon fiber microelectrodes revealed
84 lse transmitter that could be monitored with amperometry by placing the carbon fiber directly on the
85                                 Carbon-fibre amperometry can evaluate the effect of M channel activit
86 demonstrates for the first time that in vivo amperometry can measure both regional brain tissue O2 le
87  to tBLMs by pulsed or ramped direct-current amperometry can, however, provide current-voltage (I/V)
88         Cyclic voltammetry, when compared to amperometry, can provide excellent chemical resolution;
89  and single cell carbon-fiber microelectrode amperometry (CFMA).
90                               Potential step amperometry (chronoamperometry) of the Tl(I)/Tl(Hg) elec
91 in calf chromaffin cells using catecholamine amperometry combined with different patterns of stimulat
92   These events, which manifest themselves in amperometry, correspond to the formation of electrocatal
93                       Cyclic voltammetry and amperometry demonstrate excellent electrocatalytic activ
94  and safe Ion Exchange Chromatography-Pulsed Amperometry Detection (IC-PAD) method for direct determi
95 iode array absorbance and constant potential amperometry detectors was further tested on the fast-sca
96                                 Carbon-fiber amperometry detects oxidizable molecules released by exo
97 ear scan voltammetry (LSV) or flow injection amperometry (FIamp) at constant applied potential.
98 ant limitation when using constant-potential amperometry for biosensor application such as amperometr
99 etection of analytes and combining FSCV with amperometry for the detection of dopamine.
100                                 Carbon-fiber amperometry has been extensively used to monitor the tim
101                           Fifth, single-cell amperometry has revealed secretion kinetics with submill
102                                              Amperometry, histology, and short-circuit current measur
103                 This combination of SERS and amperometry in a single device provides an improved meth
104 was assessed through the use of carbon fibre amperometry in combination with Fura-2.
105 size of secreted catecholamines, measured by amperometry in cultured chromaffin cells, was found to b
106 nce of ferricyanide and finally ferrocyanide amperometry in drug-free buffer.
107 ontal and motor cortex using fixed-potential amperometry in freely behaving rats.
108                           We used high-speed amperometry in freely moving rats to examine the effects
109 ies, using fMRI in humans and in vivo oxygen amperometry in rats.
110 n the biosensor was used in conjunction with amperometry in stirred solution for the analysis of seru
111                                 Carbon fiber amperometry is a popular method for measuring single exo
112               These experiments suggest that amperometry is a useful technique for studying, in real
113                          Herein, single-cell amperometry is employed to characterize the dynamic secr
114 e more commonly used constant potential (DC) amperometry is made.
115    In this work, carbon-fiber microelectrode amperometry is used to characterize serotonin exocytosis
116                                              Amperometry is used widely to study neurotransmitter dis
117                                              Amperometry is widely used to study exocytosis of neurot
118 inergic exocytosis, measured by carbon fibre amperometry, is synchronized to an AP.
119 nces between these and results obtained with amperometry may indicate that amperometry and capacitanc
120                               In vivo oxygen amperometry measurements in the ventral striatum in awak
121  present in food products was carried out by amperometry method in which reduction potential was fixe
122                                          The amperometry method showed an excellent performance with
123     A sensitive and time-saving hydrodynamic amperometry method was developed for the determination o
124 on of oxalic acid (80 nA/nM) achieved by the amperometry method.
125 roelectrode fast-scan cyclic voltammetry and amperometry methods correlated with transmission electro
126 oamperometry (CA) and open circuit potential amperometry (OCPA).
127 ernal reflection fluorescence microscopy and amperometry of released catecholamine.
128  single cells in culture, constant potential amperometry offers the best temporal resolution, and a l
129 stigated by cyclic voltammetry and transient amperometry on a Pt ultramicroelectrode in aqueous solut
130 n the whole-cell configuration combined with amperometry on human embryonic kidney HEK-293 cells stab
131 arding the present application is the use of amperometry on inside-out patches with synchronous recor
132 calibrated for Rexocytosis using single cell amperometry on parallel cell cultures.
133  the case of anti-hGH detection using pulsed amperometry (PA) with 3,3',5,5'-tetramethylbenzidine (TM
134                         Thus, in vivo oxygen amperometry permits a novel, stable form of longitudinal
135 analytical determinations by fixed potential amperometry, phosphate buffer saline being the best.
136                               A differential amperometry protocol is optimized to improve selectivity
137           To explore these questions we used amperometry recording from PC12 cells to investigate the
138                                              Amperometry recording showed that during exocytosis in c
139                                              Amperometry result shows that the RGO@PDA composite dete
140                                 Furthermore, amperometry revealed a delay in fusion pore expansion.
141                                 Carbon fiber amperometry revealed that release of dopamine was quanta
142                                              Amperometry revealed that the expression of tPA-green fl
143        Analysis of noradrenalin secretion by amperometry showed that inhibitory mutants of SCAMP2 dec
144                             By acquiring the amperometry signal with a high sampling rate of 100 Hz w
145                       Cyclic voltammetry and amperometry studies confirmed the electrocatalytic natur
146                                              Amperometry studies show that the SRGO/GCE electrode is
147  to detect the enzyme product TMB/H2O2 using amperometry, successfully reproducing the colorimetry-ob
148                           Recent advances in amperometry techniques have revealed phasic ACh releases
149                                         With amperometry, the concentration gradient created by the e
150                 As monitored by carbon-fibre amperometry, the sustained [Ca(2+)](i) increase stimulat
151                                        Using amperometry to analyze exocytosis, we show that expressi
152 havioral analyses, pharmacology, and in vivo amperometry to assess the role of SLC10A4 in dopamine-re
153                Finally, we used enzyme-based amperometry to demonstrate reduced cholinergic neurotran
154  one type of anion is accomplished by pulsed amperometry to ensure a rapid, repetitive renewal of the
155 study of mechanisms of toxin action, we used amperometry to examine secretion of catecholamines and s
156 observations, we have used microcarbon fiber amperometry to examine secretogogue-induced 5-HT release
157  the effects of Ca(2+) on fusion pores using amperometry to follow the exocytosis of single vesicles
158  address this question, we used carbon fiber amperometry to measure catecholamine secretion evoked by
159 r chains and examined the consequences using amperometry to measure fusion pore opening and dilation.
160                              We used in vivo amperometry to monitor changes in synaptic dopamine (DA)
161 regulates fusion pores was investigated with amperometry to monitor exocytosis of single dense-core v
162 ive depolarizing stimuli were compared using amperometry to monitor vesicular release events and intr
163 nctioning fusion pores, we used carbon fibre amperometry to record pre-spike feet, which have been sh
164 eveloped an approach to study it directly by amperometry using carbon fiber microelectrodes in organo
165 by cyclic voltammetry and constant potential amperometry using hydrolyzed methyl salicylate as the an
166                                              Amperometry, voltammetry, and impedance spectroscopy rep
167                           Constant potential amperometry was also used to evaluate durability, repeat
168                                              Amperometry was also used to evaluate the analytical per
169  exocytotic peaks, observed with single cell amperometry, was investigated.
170                     Using constant potential amperometry, we examined the effects of the NMDA recepto
171                           Using carbon fiber amperometry, we found that exocytosis is impaired at the
172  By combining the patch-clamp technique with amperometry, we measured DA release under voltage clamp.
173 d ceramic MEAs coupled with constant voltage amperometry, we measured resting glutamate levels and sy
174 by cyclic voltammetry and constant potential amperometry were 112.37 and 282.82muAcm(-2)mM(-1) respec
175                              Voltammetry and amperometry were applied under flow and no flow conditio
176                 Cyclic voltammogram (CV) and amperometry were employed to study electrochemical prope
177            Meanwhile, cyclic voltammetry and amperometry were used to check on the performances of th
178                  Cyclic voltammetry (CV) and amperometry were used to evaluate the catalytic activity
179 (ferrocyanide) was continuously monitored by amperometry whereas the product of the reaction (ferricy
180 .1 (n = 14) exocytotic events as measured by amperometry, whereas the inactive structural analog had
181 s was investigated using in vitro continuous amperometry with a carbon fibre microelectrode and video
182 g flow injection analysis and multiple pulse amperometry with a cathodically pretreated boron-doped d
183                                   Continuous amperometry with a diamond microelectrode and video micr
184                                              Amperometry with carbon-fiber microelectrodes provides a
185                                 On combining amperometry with perforated patch whole-cell recording,
186 emical measurements (such as voltammetry and amperometry) with high spatial resolution and sensitivit
187 an order of magnitude more sensitive than DC amperometry, with calculated mass detection limits (S/N

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