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1         Utilizing highly localized and rapid iontophoretic agonist delivery, combined with patch-clam
2 ly responsible for the inhibitory effects of iontophoretic AMPH, dopamine alone cannot account for th
3 hat observed ejections are due to the sum of iontophoretic and electroosmotic forces.
4 ns tested, 42 were inhibited (68%) following iontophoretic application of 17betaE2 in a current-depen
5 , effects which were blocked by simultaneous iontophoretic application of a glutamate receptor antago
6 ed in the human skin blood flow responses to iontophoretic application of acetylcholine (ACH; deliver
7 d beta-adrenoceptor receptor stimulation, by iontophoretic application of acetylcholine, noradrenalin
8 ase in skin perfusion observed following the iontophoretic application of ACh; and (2) stimulation of
9 attained by synaptic release of glutamate or iontophoretic application of aspartate, induced a wave o
10 g inferior colliculus (IC) before and during iontophoretic application of bicuculline, a GABA(A) rece
11 ined at two sound azimuths before and during iontophoretic application of bicuculline, an antagonist
12 eurons showing PLS before, during, and after iontophoretic application of bicuculline.
13 cording, and we labeled their projections by iontophoretic application of dextran anterograde tracers
14 e in tissue perfusion observed following the iontophoretic application of either ACh vehicle or SNP v
15 ty of IC neuron is studied before and during iontophoretic application of GABA and its antagonist, bi
16                                              Iontophoretic application of GABA consistently inhibited
17                IPSPs and the response to the iontophoretic application of GABA were found to reverse
18      Measurements were made in the ICX using iontophoretic application of glutamate receptor antagoni
19              Both effects can be mimicked by iontophoretic application of glycine.
20                                              Iontophoretic application of hcrt1 enhanced the firing r
21                                              Iontophoretic application of histamine can also cause in
22                                 Brief, focal iontophoretic application of kainate rapidly induced bea
23                                              Iontophoretic application of NE to target neurons in the
24 is latter action is generally not found with iontophoretic application of NE to target neurons or sti
25 ed by either previous whisker deflections or iontophoretic application of NMDA; both manipulations ef
26  units before, during, and after local micro-iontophoretic application of selective antagonists to AM
27 d pH-sensitive RTN neurons were activated by iontophoretic application of serotonin or substance P.
28         In the current study, the effects of iontophoretic application of the 5-HT 1A agonist 8-OH-DP
29 n the macaque prefrontal cortex by combining iontophoretic application of the general muscarinic rece
30                                      In vivo iontophoretic application of the mGluR2/3 agonists (2R,
31 es using carbon-fiber electrodes attached to iontophoretic barrels.
32                                          The iontophoretic-biosensing tattoo platform is reduced to p
33                             Passive and 2-mA iontophoretic (both cathodal and anodal) transport exper
34 tic nerve after subconjunctival injection or iontophoretic carboplatin delivery revealed significantl
35                                     A silver iontophoretic catheter (SIC) was developed consisting of
36 ies of pathway-tracing experiments involving iontophoretic co-injection of the tracers Phaseolus vulg
37  a decreased ability to penetrate skin under iontophoretic conditions.
38 membranes were measured as a function of the iontophoretic current passed across the membrane (-1.0 t
39 nce of the electric field resulting from the iontophoretic current, electroosmotic flow in the tissue
40 rt across the skin under the influence of an iontophoretic current.
41 no postsynaptic DA receptors on SNr neurons, iontophoretic DA was ineffective in altering discharge r
42 ats to assess the feasibility of transdermal iontophoretic delivery in vivo, of a lipophilic drug com
43                                        Local iontophoretic delivery of cytotoxic agents should be con
44 e iontophoretic devices and tested the local iontophoretic delivery of FOLFIRINOX for the treatment o
45                                              Iontophoretic delivery of FOLFIRINOX was found to increa
46 he sclera in approximately 2h after cathodal iontophoretic delivery of the micellar carrier systems,
47 adrenergic vasoregulation was impaired using iontophoretic delivery of tyramine, phentolamine, and br
48 as compared to the control after passive and iontophoretic delivery.
49 n in the anterior chamber and vitreous after iontophoretic delivery.
50                                        After iontophoretic deposits of biotinylated dextran amine (BD
51 lize on the unique ability of an implantable iontophoretic device to deliver much higher concentratio
52               We have fabricated implantable iontophoretic devices and tested the local iontophoretic
53  of chemotherapies has become possible using iontophoretic devices that are implanted directly onto p
54                   Determine safe, effective, iontophoretic dose(s) of EGP-437 (dexamethasone phosphat
55  doses of ATP were delivered using different iontophoretic driving currents.
56 mbination of in vivo loose-patch recordings, iontophoretic drug application, and detailed signal anal
57 nit recordings in parallel with systemic and iontophoretic drug application, and stimulation of the s
58 re hearing onset and in vivo recordings with iontophoretic drug applications after hearing onset, we
59                                              Iontophoretic dye injection experiments revealed planar
60 of DA attenuated basal firing as well as the iontophoretic effects of ACh both during the DA applicat
61                  Activity that was evoked by iontophoretic ejection of excitatory amino acids, such a
62 Neuronal activity in the LA was elicited via iontophoretic ejection of L-glutamate or synaptically vi
63                                       Often, iontophoretic ejections from micropipets into brain tiss
64 pidermal diagnostic device combining reverse iontophoretic extraction of interstitial glucose and an
65 tient-controlled analgesia pump (n = 320) or iontophoretic fentanyl hydrochloride (40- microg infusio
66  in both conditions were highly sensitive to iontophoretic GABA, but the response was stronger during
67 owing of SNpr neuron activity in response to iontophoretic GABA.
68 neurons in striatum and nucleus accumbens to iontophoretic glutamate.
69 c tract (STT) neurons selectively excited by iontophoretic histamine.
70 ce red dye, sulforhodamine 101, after pulsed iontophoretic infusion.
71 droxylase (TH) mRNA in the MZI following its iontophoretic injection into either the cAMY, HDB or PVN
72                                              Iontophoretic injection of 10% biotinylated dextran amin
73  positions of a clock face, were targeted by iontophoretic injection of fluorescent, lipophilic dye.
74 can be double-labeled with HRP and Fos after iontophoretic injection of HRP into the recording site.
75 erns of junctional communication revealed by iontophoretic injection of junction-permeable reporter m
76                                              Iontophoretic injection of Neurobiotin, a low molecular
77  by physiological assay and received a local iontophoretic injection of Neurobiotin.
78                               A single small iontophoretic injection of Phaseolus vulgaris leucoagglu
79  and LacZ-labelled cells as donor tissue and iontophoretic injection of the anterograde tracers BDA,
80          Using the single-cell recording and iontophoretic injection technique, we identified four gr
81                                              Iontophoretic injections guided by physiological recordi
82                                              Iontophoretic injections into the LP of the anterograde
83                                        Small iontophoretic injections labeled fewer neurons with the
84 ections of RTN were studied by placing small iontophoretic injections of anterograde (biotinylated de
85                                      Precise iontophoretic injections of BDA and CTB in the mSCN and
86 grade and anterograde tract tracing methods: iontophoretic injections of biocytin or biotinylated dex
87  albino rabbits and Long-Evans rats received iontophoretic injections of biotinylated dextran amine,
88                                    By making iontophoretic injections of CaCl2 we have investigated c
89 ly sized, physiologically guided pressure or iontophoretic injections of cholera toxin subunit B (CTb
90 ibution was examined using single unilateral iontophoretic injections of cholera toxin subunit B.
91 uridine (BrdU), animals received stereotaxic iontophoretic injections of Fluoro-Gold (FG) into field
92                                Intracellular iontophoretic injections of Lucifer yellow were performe
93  M pathways to the CO-blobs) were labeled by iontophoretic injections of Phaseolus vulgaris leucoaggl
94                                              Iontophoretic injections of Phaseolus vulgaris leucoaggl
95  The present study used localized, intra-SCN iontophoretic injections of the anterograde tracer bioti
96                                              Iontophoretic injections of the anterograde tracer Phase
97                                              Iontophoretic injections of the anterograde tracers Phas
98 injections and electrophysiologically guided iontophoretic injections of the anterograde tract tracer
99  transynaptic analysis of circuits and small iontophoretic injections of the conventional tracer hors
100 it responses to sound in the ICC with focal, iontophoretic injections of the retrograde tracer Fluoro
101          Male hamsters received stereotaxic, iontophoretic injections of the retrograde tracer, chole
102    Geniculocortical K axons were labeled via iontophoretic injections of wheat germ agglutinin-horser
103 ical parameters were used for our sequential iontophoretic injections, producing injections of AAV th
104                           Using a dual-color iontophoretic labeling strategy, we found that the preci
105                                        Using iontophoretic labelling of neural crest cells, we demons
106 er including the authors' data and published iontophoretic measurements in a simple model of diffusio
107  behavior during meiosis, was revealed after iontophoretic microinjection of rhodamine-conjugated (rh
108 ng PACAP innervation to the rat PVN by using iontophoretic microinjections of the retrograde neuroana
109                                              Iontophoretic NE inhibited all vSub neurons tested, wher
110 o study the cellular mechanisms, we combined iontophoretic pharmacological analysis of cholinergic re
111                           Multi-barrel glass iontophoretic pipettes were used to record single neuron
112 oelectrode incorporated into a multibarreled iontophoretic probe to detect the ejection of electroact
113               The depolarization produced by iontophoretic pulses of ACh was scarcely changed by 3000
114                     Here we apply short (2s) iontophoretic pulses of glutamate, GABA, dopamine and do
115 ed by activation of D2 receptors, effects of iontophoretic quinpirole were examined after various tre
116                        GABA had no effect on iontophoretic responses to glutamate and decreased the c
117                                              Iontophoretic studies cataloged potential NE effects; ho
118 aluated for its potential in the MN mediated iontophoretic transdermal delivery.
119 ss mouse skin) recorded during diffusive and iontophoretic transport, are reported.
120 raocular tumor was observed after repetitive iontophoretic treatment.
121 ETATAG mice underwent a total of six, serial iontophoretic treatments administered two times per week

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