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1 hile glucose down to 17 muM (CL) and 40 muM (amperometry).
2  conductivity, which was monitored by pulsed amperometry.
3 -noise ratio = 3) using controlled potential amperometry.
4 lection fluorescence microscopy (pTIRFM) and amperometry.
5 nhanced neurotransmitter release measured by amperometry.
6  efflux comparable with hDAT was detected by amperometry.
7 by measurements of [(3)H]dopamine efflux and amperometry.
8 sing a diamond microelectrode and continuous amperometry.
9  on the ITO electrode beneath the cell using amperometry.
10 amphetamine-induced DA efflux as measured by amperometry.
11  or 3.2 x 10(10) viral particles/mL with RDE amperometry.
12  ventral midbrain neurons using carbon fiber amperometry.
13 ll capacitance measurements and carbon fibre amperometry.
14  observations of insulin release detected by amperometry.
15 m chromaffin cells using cell-attached patch amperometry.
16 olamine measured with cyclic voltammetry and amperometry.
17  detected by means of cyclic voltammetry and amperometry.
18 n and directly detected by integrated pulsed amperometry.
19 do-1 microfluorometry and constant potential amperometry.
20 gated by normal-pulse voltammetry and pulsed amperometry.
21 capacitance, FM1-43 fluorescence imaging and amperometry.
22 ntaneous and evoked quantal release of DA by amperometry.
23 nts of exocytosis obtained simultaneously by amperometry.
24 es and small vesicles, has been studied with amperometry.
25 ous indo-1 photometry and constant potential amperometry.
26 hed dye, and catecholamines were detected by amperometry.
27 elease of vesicular contents was followed by amperometry.
28 ochemical techniques: cyclic voltammetry and amperometry.
29 rent spikes by the electrochemical method of amperometry.
30 tain new measurements of vesicle content via amperometry.
31 strated with cyclic voltammetry (CV) and i-t amperometry.
32 the area under the curve (AUC) observed with amperometry.
33 ammetry, differential pulse voltammetry, and amperometry.
34 ip coupled to a miniature potentiostat using amperometry.
35 ing stochastic single-nanoparticle collision amperometry.
36 ely to act as the major detected compound in amperometry.
37 stepwise increases in current as observed by amperometry.
38 ule release with carbon-fiber microelectrode amperometry.
39 ric oxide (NO) production was assessed using amperometry.
40 icosities in the Drosophila larval system by amperometry.
41 erface was studied by cyclic voltammetry and amperometry.
42 b sulfide were achieved using flow injection amperometry.
43 her cyclic voltammetry or constant potential amperometry.
44  were studied by cyclic voltammetry (CV) and amperometry.
45 ipally with disk carbon fiber microelectrode amperometry.
46 ermined from direct glucose injection during amperometry.
47 he electrochemical detection is performed by amperometry (-0.20 V vs Ag pseudoreference electrode) at
48 ddress this question, we used in vivo oxygen amperometry, a proxy for blood oxygen level-dependent (B
49                                       Pulsed amperometry allowed a direct detection of the carbohydra
50                                              Amperometry allowed the quantification of the content re
51  detected with rotating disk electrode (RDE) amperometry and an interdigitated array (IDA) electrode.
52 or other electrochemical techniques, such as amperometry and aptamer-based sensing.
53  obtained with amperometry may indicate that amperometry and capacitance detect the fusion of differe
54 h-clamped PC12 cells was analyzed using both amperometry and capacitance measurements.
55 holamine secretion was measured by oxidative amperometry and cell membrane turnover was measured by v
56 is mutant were characterized by carbon fiber amperometry and cell-attached patch capacitance measurem
57 1E mutants were investigated by carbon fiber amperometry and cell-attached patch capacitance measurem
58 chievements to boost analytical performance, amperometry and chemiluminescence (CL)-based biosensors
59                                         Here amperometry and conductance measurements were performed
60  and it demonstrates that the combination of amperometry and constant-impedance SECM has the potentia
61                               Flow injection amperometry and cyclic voltammetry were used to assess a
62 imilar when measured with constant potential amperometry and cyclic voltammetry.
63 ons for stimulated release of dopamine using amperometry and cyclic voltammetry.
64 rflow in striatal slices by using continuous amperometry and cyclic voltammetry.
65         The results from cyclic voltammetry, amperometry and electrochemical impedance spectroscopy d
66 lytical methods (potentiometry, voltammetry, amperometry and electrochemical impedance spectroscopy)
67                                         Both amperometry and electron micrograph data were analyzed b
68 2 cells using alternately constant-potential amperometry and fast-scan cyclic voltammetry (FSCV).
69  edge findings and technological advances in amperometry and fast-scan cyclic voltammetry.
70 anges were compared using constant potential amperometry and fast-scan cyclic voltammetry.
71 ent bonding and detection techniques such as amperometry and fluorescence measurements are discussed
72                                        Using amperometry and FMRFamide tagging, I simultaneously meas
73  crosstalk between electrodes when comparing amperometry and FSCV.
74 rsors, and metabolites, were evaluated using amperometry and high performance liquid chromatography w
75 using capacitance measurements combined with amperometry and stimulation by flash photolysis of caged
76 ydrogen peroxide (H(2)O(2)) was evaluated by amperometry and the so-made amperometric biosensor was a
77 ved measurements in situ, techniques such as amperometry and traditional field-effect detection requi
78                                              Amperometry and transmission electron microscopy have be
79                                              Amperometry and transmission electron microscopy have be
80 ypical millimolar concentrations employed in amperometry and voltammetry.
81 s for glucose oxidation using flow injection amperometry and voltammetry.
82 to perform electrochemical measurements like amperometry and voltammetry.
83 gen peroxide (4 pmol for CL and 210 pmol for amperometry) and zeptomoles of HRP (45 zmol for CL and 2
84 studied by confocal fluorescence microscopy, amperometry, and cell-attached capacitance measurements.
85 erent media by chronoamperometry, multipulse amperometry, and chronopotentiometry, respectively at ca
86                High-speed chronoamperometry, amperometry, and differential pulse voltammetry were use
87 ctrochemical techniques (cyclic voltammetry, amperometry, and differential pulse voltammetry) and dif
88 broad spectrum of viruses using voltammetry, amperometry, and electrochemical impedance spectroscopy.
89                Employing cyclic voltammetry, amperometry, and FTIR with various electrolytes of varyi
90 including voltammetry, enzyme-based sensors, amperometry, and in vivo microdialysis, there is current
91                         This was detected by amperometry, and it was found to be accompanied by Ca2+
92 ating ion-selective electrodes, carbon fiber amperometry, and magnetic resonance imaging, we monitore
93 nd glucose, respectively, using voltammetry, amperometry, and potentiometry.
94 racterized using finite element simulations, amperometry, and Raman experiments.
95 differentiated PC12 cells using carbon-fiber amperometry, and relative diameters of individual vesicl
96 ammetry (CV), square wave voltammetry (SWV), amperometry, and square wave anodic stripping voltammetr
97                                              Amperometry approach curve profiling coupled with classi
98   We established a new measurement approach, amperometry approach curve profiling, which monitors the
99  secretion from single cells was detected by amperometry as a series of current spikes corresponding
100 with the introduction of reliable and robust amperometry as a valuable alternative to existing potent
101      We propose pulse power generation (PPG) amperometry as an advanced readout realized for Prussian
102  from chromaffin cells by constant potential amperometry as well as fast-scan cyclic voltammetry.
103                                              Amperometry at -200 mV (vs the Ag pseudo-reference elect
104 were evaluated by dynamic constant potential amperometry at 1.3V under non-buffered conditions.
105 re determined by cyclic voltammetry (CV) and amperometry at a custom thin-layer cell (TLC) detector.
106                                              Amperometry at a rotating disk electrode at 0 V gave sen
107                         GluA was measured by amperometry at a working potential of 0.6 V vs Ag/AgCl.
108                                              Amperometry at the carbon fiber microelectrodes revealed
109 lse transmitter that could be monitored with amperometry by placing the carbon fiber directly on the
110                                 Carbon-fibre amperometry can evaluate the effect of M channel activit
111 demonstrates for the first time that in vivo amperometry can measure both regional brain tissue O2 le
112  to tBLMs by pulsed or ramped direct-current amperometry can, however, provide current-voltage (I/V)
113         Cyclic voltammetry, when compared to amperometry, can provide excellent chemical resolution;
114  and single cell carbon-fiber microelectrode amperometry (CFMA).
115                               Potential step amperometry (chronoamperometry) of the Tl(I)/Tl(Hg) elec
116 in calf chromaffin cells using catecholamine amperometry combined with different patterns of stimulat
117   These events, which manifest themselves in amperometry, correspond to the formation of electrocatal
118 of fusion pore dynamics, a transformation of amperometry current was introduced that yields fusion po
119 g the use of voltammetric techniques such as amperometry, cyclic and linear scan, differential pulse,
120                                        Using amperometry, cyclic voltammetry (CV), and X-ray photoele
121 tion, has been predominantly performed using amperometry, cyclic voltammetry, or differential pulse v
122                       Cyclic voltammetry and amperometry demonstrate excellent electrocatalytic activ
123  and safe Ion Exchange Chromatography-Pulsed Amperometry Detection (IC-PAD) method for direct determi
124 -exchange chromatography coupled with pulsed amperometry detection, we observed that both enzymes hav
125 iode array absorbance and constant potential amperometry detectors was further tested on the fast-sca
126                                 Carbon-fiber amperometry detects oxidizable molecules released by exo
127 roanalytical techniques, cyclic voltammetry, amperometry, differential pulse voltammetry, and square
128                      Under these conditions, amperometry, epifluorescence imaging, and ECL imaging we
129 ear scan voltammetry (LSV) or flow injection amperometry (FIamp) at constant applied potential.
130 ant limitation when using constant-potential amperometry for biosensor application such as amperometr
131 ), differential pulse voltammetry (DPV), and amperometry for detecting of Vitamin D3.
132 hanges in exocytosis observed by single-cell amperometry for different counteranions.
133 etection of analytes and combining FSCV with amperometry for the detection of dopamine.
134                                      Herein, amperometry has been applied to show that the vesicular
135                                 Carbon-fiber amperometry has been extensively used to monitor the tim
136                           Fifth, single-cell amperometry has revealed secretion kinetics with submill
137                                              Amperometry, histology, and short-circuit current measur
138  nM) for the determination of DZ through the amperometry (i-t) method.
139 moles of HRP (45 zmol for CL and 20 zmol for amperometry); IgG was detected down to 12 fM (CL) and 12
140 SRS was much greater than that obtained from amperometry, implying that liposomes may release only a
141                 This combination of SERS and amperometry in a single device provides an improved meth
142 thods including cyclical voltammetry and i-t amperometry in artificial cerebrospinal fluid (ACSF) sol
143 was assessed through the use of carbon fibre amperometry in combination with Fura-2.
144                                              Amperometry in conjunction with total internal reflectio
145 size of secreted catecholamines, measured by amperometry in cultured chromaffin cells, was found to b
146 nce of ferricyanide and finally ferrocyanide amperometry in drug-free buffer.
147 ontal and motor cortex using fixed-potential amperometry in freely behaving rats.
148                           We used high-speed amperometry in freely moving rats to examine the effects
149        Here, we used in vivo fixed potential amperometry in male Long-Evans rats to test if phasic nu
150 cs of DCV exocytosis by using single-vesicle amperometry in PC12 cells (derived from the pheochromocy
151  used oxygen sensors coupled with high-speed amperometry in rats of both sexes to explore the treatme
152 ies, using fMRI in humans and in vivo oxygen amperometry in rats.
153 n the biosensor was used in conjunction with amperometry in stirred solution for the analysis of seru
154          In this article, intermittent pulse amperometry (IPA) is utilized to perform millisecond-res
155                                 Carbon fiber amperometry is a popular method for measuring single exo
156                      Traditional single-cell amperometry is a powerful technique for studying the mol
157               These experiments suggest that amperometry is a useful technique for studying, in real
158                          Herein, single-cell amperometry is employed to characterize the dynamic secr
159 e more commonly used constant potential (DC) amperometry is made.
160    In this work, carbon-fiber microelectrode amperometry is used to characterize serotonin exocytosis
161                                              Amperometry is used widely to study neurotransmitter dis
162                                              Amperometry is widely used to study exocytosis of neurot
163 inergic exocytosis, measured by carbon fibre amperometry, is synchronized to an AP.
164 nces between these and results obtained with amperometry may indicate that amperometry and capacitanc
165                               In vivo oxygen amperometry measurements in the ventral striatum in awak
166  present in food products was carried out by amperometry method in which reduction potential was fixe
167                                          The amperometry method showed an excellent performance with
168 ar range of 1.25-487.5 and 587.5-1500 muM in amperometry method towards vanillin detection.
169     A sensitive and time-saving hydrodynamic amperometry method was developed for the determination o
170 on of oxalic acid (80 nA/nM) achieved by the amperometry method.
171 roelectrode fast-scan cyclic voltammetry and amperometry methods correlated with transmission electro
172                           Based on the (i-t) amperometry mode, NADH can be quantified with a linear r
173 oamperometry (CA) and open circuit potential amperometry (OCPA).
174                            Redox voltammetry/amperometry of excellent quality was achieved in static
175 ernal reflection fluorescence microscopy and amperometry of released catecholamine.
176  single cells in culture, constant potential amperometry offers the best temporal resolution, and a l
177 stigated by cyclic voltammetry and transient amperometry on a Pt ultramicroelectrode in aqueous solut
178 n the whole-cell configuration combined with amperometry on human embryonic kidney HEK-293 cells stab
179 arding the present application is the use of amperometry on inside-out patches with synchronous recor
180 calibrated for Rexocytosis using single cell amperometry on parallel cell cultures.
181     A similar experiment was performed using amperometry on ultramicroelectrodes (UMEs).
182  the case of anti-hGH detection using pulsed amperometry (PA) with 3,3',5,5'-tetramethylbenzidine (TM
183                         Thus, in vivo oxygen amperometry permits a novel, stable form of longitudinal
184 analytical determinations by fixed potential amperometry, phosphate buffer saline being the best.
185 uding ion-selective potentiometry, enzymatic amperometry, potential sweep voltammetry, field-effect t
186 of high-resolution capacitance measurements, amperometry, protein expression/gene knock out/down, res
187                               A differential amperometry protocol is optimized to improve selectivity
188           To explore these questions we used amperometry recording from PC12 cells to investigate the
189 ated the mechanisms of this inhibition using amperometry recording of Ca(2+)-triggered catecholamine
190                       The present study used amperometry recording of catecholamine release from endo
191                                              Amperometry recording reveals the exocytosis of catechol
192                                              Amperometry recording showed that during exocytosis in c
193                                              Amperometry result shows that the RGO@PDA composite dete
194                                 Furthermore, amperometry revealed a delay in fusion pore expansion.
195                                 Carbon fiber amperometry revealed that release of dopamine was quanta
196                                              Amperometry revealed that the expression of tPA-green fl
197            We employed real-time single-cell amperometry (SCA) with microsensors to quantitatively an
198        Analysis of noradrenalin secretion by amperometry showed that inhibitory mutants of SCAMP2 dec
199                                              Amperometry shows that the vesicular content increases a
200                             By acquiring the amperometry signal with a high sampling rate of 100 Hz w
201                       Cyclic voltammetry and amperometry studies confirmed the electrocatalytic natur
202                                              Amperometry studies show that the SRGO/GCE electrode is
203  to detect the enzyme product TMB/H2O2 using amperometry, successfully reproducing the colorimetry-ob
204                           Recent advances in amperometry techniques have revealed phasic ACh releases
205                                         With amperometry, the concentration gradient created by the e
206                                        Using amperometry, the sub-millisecond dynamics of exocytosis
207                 As monitored by carbon-fibre amperometry, the sustained [Ca(2+)](i) increase stimulat
208                                        Using amperometry to analyze exocytosis, we show that expressi
209 havioral analyses, pharmacology, and in vivo amperometry to assess the role of SLC10A4 in dopamine-re
210 proach to sensor design enables battery-free amperometry to be integrated with chip-free wireless dat
211                Finally, we used enzyme-based amperometry to demonstrate reduced cholinergic neurotran
212 ith a redox mediator, ferrocyanide, and used amperometry to detect their collision on a carbon-fiber
213  one type of anion is accomplished by pulsed amperometry to ensure a rapid, repetitive renewal of the
214 study of mechanisms of toxin action, we used amperometry to examine secretion of catecholamines and s
215 observations, we have used microcarbon fiber amperometry to examine secretogogue-induced 5-HT release
216  the effects of Ca(2+) on fusion pores using amperometry to follow the exocytosis of single vesicles
217                       In this study, we used amperometry to investigate the mechanism by which somato
218 ion and dense-core vesicle function, we used amperometry to measure catecholamine release from single
219  address this question, we used carbon fiber amperometry to measure catecholamine secretion evoked by
220 r chains and examined the consequences using amperometry to measure fusion pore opening and dilation.
221                              We used in vivo amperometry to monitor changes in synaptic dopamine (DA)
222 regulates fusion pores was investigated with amperometry to monitor exocytosis of single dense-core v
223 ive depolarizing stimuli were compared using amperometry to monitor vesicular release events and intr
224 nctioning fusion pores, we used carbon fibre amperometry to record pre-spike feet, which have been sh
225 e, we used a translational technique, oxygen amperometry, to record haemodynamic signals in the nucle
226 eveloped an approach to study it directly by amperometry using carbon fiber microelectrodes in organo
227 by cyclic voltammetry and constant potential amperometry using hydrolyzed methyl salicylate as the an
228 e synthesized on a gold surface by multistep amperometry using the optimized conditions and in-house
229                                              Amperometry, voltammetry, and impedance spectroscopy rep
230 h different electrochemical probing methods (amperometry, voltammetry, and potentiometry) and demonst
231                           Constant potential amperometry was also used to evaluate durability, repeat
232                                              Amperometry was also used to evaluate the analytical per
233  exocytotic peaks, observed with single cell amperometry, was investigated.
234                                         With amperometry, we discovered that reactive oxygen species
235                     Using constant potential amperometry, we examined the effects of the NMDA recepto
236                           Using carbon fiber amperometry, we found that exocytosis is impaired at the
237  By combining the patch-clamp technique with amperometry, we measured DA release under voltage clamp.
238 d ceramic MEAs coupled with constant voltage amperometry, we measured resting glutamate levels and sy
239 by cyclic voltammetry and constant potential amperometry were 112.37 and 282.82muAcm(-2)mM(-1) respec
240                              Voltammetry and amperometry were applied under flow and no flow conditio
241                 Cyclic voltammogram (CV) and amperometry were employed to study electrochemical prope
242            Meanwhile, cyclic voltammetry and amperometry were used to check on the performances of th
243                  Cyclic voltammetry (CV) and amperometry were used to evaluate the catalytic activity
244        Electrical stimulation and continuous amperometry were used to measure NO release from myenter
245 (ferrocyanide) was continuously monitored by amperometry whereas the product of the reaction (ferricy
246 .1 (n = 14) exocytotic events as measured by amperometry, whereas the inactive structural analog had
247 ic voltammetry, square wave voltammetry, and amperometry while being controlled by custom-made softwa
248  was detected down to 12 fM (CL) and 120 fM (amperometry), while glucose down to 17 muM (CL) and 40 m
249 s was investigated using in vitro continuous amperometry with a carbon fibre microelectrode and video
250 g flow injection analysis and multiple pulse amperometry with a cathodically pretreated boron-doped d
251                                   Continuous amperometry with a diamond microelectrode and video micr
252                                              Amperometry with carbon-fiber microelectrodes provides a
253  Ag/AgCl/3 M KCl, enabling cathodic H(2)O(2) amperometry with good target proportionality.
254                                 On combining amperometry with perforated patch whole-cell recording,
255 emical measurements (such as voltammetry and amperometry) with high spatial resolution and sensitivit
256 an order of magnitude more sensitive than DC amperometry, with calculated mass detection limits (S/N

 
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