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2 ly responsible for the inhibitory effects of iontophoretic AMPH, dopamine alone cannot account for th
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
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
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.
29 n the macaque prefrontal cortex by combining iontophoretic application of the general muscarinic rece
34 tic nerve after subconjunctival injection or iontophoretic carboplatin delivery revealed significantl
36 ies of pathway-tracing experiments involving iontophoretic co-injection of the tracers Phaseolus vulg
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
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
44 e iontophoretic devices and tested the local iontophoretic delivery of FOLFIRINOX for the treatment o
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
51 lize on the unique ability of an implantable iontophoretic device to deliver much higher concentratio
53 of chemotherapies has become possible using iontophoretic devices that are implanted directly onto p
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
60 of DA attenuated basal firing as well as the iontophoretic effects of ACh both during the DA applicat
62 Neuronal activity in the LA was elicited via iontophoretic ejection of L-glutamate or synaptically vi
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
71 droxylase (TH) mRNA in the MZI following its iontophoretic injection into either the cAMY, HDB or PVN
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
79 and LacZ-labelled cells as donor tissue and iontophoretic injection of the anterograde tracers BDA,
84 ections of RTN were studied by placing small iontophoretic injections of anterograde (biotinylated de
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,
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
93 M pathways to the CO-blobs) were labeled by iontophoretic injections of Phaseolus vulgaris leucoaggl
95 The present study used localized, intra-SCN iontophoretic injections of the anterograde tracer bioti
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
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
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
110 o study the cellular mechanisms, we combined iontophoretic pharmacological analysis of cholinergic re
112 oelectrode incorporated into a multibarreled iontophoretic probe to detect the ejection of electroact
115 ed by activation of D2 receptors, effects of iontophoretic quinpirole were examined after various tre
121 ETATAG mice underwent a total of six, serial iontophoretic treatments administered two times per week
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