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1                                The effect of iontophoretically administered glutamate on the activity
2 sed 214 microM VIP(10-28) alone and with the iontophoretically administered muscarinic receptor antag
3 orded single- and multi-unit activity whilst iontophoretically administering dopaminergic agonists an
4                           In the intact rat, iontophoretically applied 5-HT inhibited both synaptical
5              To address this, the effects of iontophoretically applied CP-99,994 (a NK-1 receptor ant
6 e exhibit a decreased inhibitory response to iontophoretically applied DA, demonstrating altered DA r
7 udies the skin microcirculation responses to iontophoretically applied drug vehicle (1 site) and drug
8 thalamus (VPL) were tested for excitation by iontophoretically applied excitatory amino acid agonists
9 In addition, in several cells the effects of iontophoretically applied excitatory amino acid antagoni
10 e 200 nM ANGII did not increase responses to iontophoretically applied GABA, the effect of ANGII on T
11 used a reduction in the size of responses to iontophoretically applied GABA, which was indistinguisha
12  fully inhibited by endogenously released or iontophoretically applied GABA.
13                                              Iontophoretically applied GLU (0-40 nA, 20 s) excited al
14 ailed to modulate the excitations induced by iontophoretically applied glutamate suggesting that SP m
15 tivity in the LA was recorded in response to iontophoretically applied glutamate.
16                                              Iontophoretically applied NE inhibited (40% of the cells
17 r-cGMP enhanced the responses of neurones to iontophoretically applied NMDA and AMPA.
18 ance postsynaptic depolarizations induced by iontophoretically applied NMDA; and (3) bath exposure to
19                                              Iontophoretically applied PE inhibited (46% of the cells
20 ), a midbrain auditory nexus, the effects of iontophoretically applied serotonin on first-spike laten
21      It also was determined that even though iontophoretically applied SP increased the spontaneous a
22 R signalling occurs significantly earlier in iontophoretically applied than in electrically evoked sy
23                                           We iontophoretically applied the general cholinergic recept
24 ncy of spinal nocifensive reflexes and, when iontophoretically applied, alter the firing of RVM ON bu
25                                              Iontophoretically-applied (-)-baclofen disproportionatel
26 ut affecting the response of SNpr neurons to iontophoretically-applied GABA.
27 esent study were to determine the effects of iontophoretically-applied noradrenergic agonists on the
28 when we bypassed the presynaptic terminal by iontophoretically applying GABA, indicating that postsyn
29 stimulation were reduced by LY382884 applied iontophoretically at the recording site.
30 Group II and III mGlu receptors were applied iontophoretically at the recording site.
31 il of anterograde and retrograde tracers was iontophoretically delivered into the medial CEA (CEAm),
32 nges in spontaneous, synaptically driven and iontophoretically driven firing were examined.
33 vity of postsynaptic receptors, as tested by iontophoretically ejected GABA, nor by elevating resting
34 uroanatomical study in which PHA-L was first iontophoretically ejected into either the lateral or ven
35 the thiol-gold linkage, and the hybrids were iontophoretically eluted from the nanoporous matrix.
36                                    MSNs were iontophoretically filled with Lucifer yellow and spines
37 ol, were lightly fixed, and VMH neurons were iontophoretically filled with Lucifer yellow.
38 teral geniculate nucleus (dLGN) were applied iontophoretically in vivo.
39 precursor cells, fluorescent vital dyes were iontophoretically injected at specific sites in the derm
40 igated by using the anterograde transport of iontophoretically injected biocytin.
41 ase (WGA-HRP), BDA, or a fluorescent tracer, iontophoretically injected into the VCN.
42   Thus, biotinylated dextran amine (BDA) was iontophoretically injected into the ventral medulla and
43                 Three weeks after tracer was iontophoretically injected into two to four sites within
44                                           We iontophoretically injected Lucifer yellow into several t
45                                           We iontophoretically injected various GABAergic and glutama
46 gically identified cutaneous afferents to be iontophoretically injected with Neurobiotin for subseque
47                     Neurobiotin was injected iontophoretically into saccular afferents of toadfish (O
48 ) fluorescent latex microbeads were injected iontophoretically or by pressure pulses (10 ms at 20 psi
49                        Retrograde tracer was iontophoretically or pressure ejected from glass micropi
50  direct action of the drug, AMPH was applied iontophoretically to neostriatal and accumbal neurons un
51 lution (pH 7.4, room temperature) and loaded iontophoretically with fura-2 to determine [Ca(2+)](i).
52 e right ventricles of rat hearts were loaded iontophoretically with fura-2 to determine [Ca2+]i.