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1                      No cells were activated antidromically.
2 ifteen right ventrobasal thalamic units were antidromically activated and 34 units orthodromically ac
3    Ten of twelve bNS neurons tested could be antidromically activated by electrical stimulation of th
4 y-three EPI ADR SPNs and 25 NE ADR SPNs were antidromically activated by stimulation of left adrenal
5     Some non-bursting subicular neurons were antidromically activated by stimuli applied to dMEC, but
6                     Some bursting cells were antidromically activated by stimuli applied to the super
7 y from 26 hypoglossal motoneurons which were antidromically activated following electrical stimulatio
8 ype II ventral pallidal neurons and could be antidromically activated from cortex or substantia nigra
9                  Of 21 MnPO neurons, 19 were antidromically activated from the hypothalamic paraventr
10          Only 9.5% of MnPO-PVN neurones were antidromically activated from the PVN bilaterally.
11           Of 65 MnPO neurones, 50 units were antidromically activated from the PVN with an average on
12 n, with strong cardiac-related activity, was antidromically activated from the spinal cord and receiv
13 e firing of MRF neurons whose axons could be antidromically activated from the vicinity of diaphragm
14 d extracellularly from medullary raphe cells antidromically activated from the XII nucleus region.
15 orded from 73 C1-C2 neurons whose axons were antidromically activated in lumbar segments.
16                   Intracellular records from antidromically activated levator motoneurons revealed th
17 rane properties and conduction velocities of antidromically activated medial septum-diagonal band (MS
18 ogenic chemicals) stimuli were recorded from antidromically activated PSDC and VLF neurons in the T(3
19                    Thirty-three neurons were antidromically activated using pulses of < or =30 microA
20 tral point from which the MZ neuron could be antidromically activated was surrounded by stimulating t
21  the raphe obscurus and pallidus nuclei were antidromically activated with latencies characteristic o
22 fied as VII motoneurons and fifteen were non-antidromically activated.
23 n of a new shoulder site in deafferented FBS antidromically-activated a cell in the former forepaw te
24 n, microstimulation delivered to forepaw VPL antidromically-activated cells in shoulder receptive fie
25 es were identified as spinally projecting by antidromically activating their axons via a stimulating
26 sympathetic nerves; this activity propagates antidromically along nerve fibers into the feed arteries
27 ic nucleus oxytocin neurones were identified antidromically and by an excitatory response to intraven
28     These non-DA neurons were activated both antidromically and orthodromically by stimulation of the
29 y-nine corticospinal neurons were identified antidromically as pyramidal tract neurons (PTNs).
30     Thirty-three RMC neurons were identified antidromically as rubrospinal (RMC-spinal) cells by stim
31  result of mechanosensory stimulation spread antidromically back through electrical junctions to unst
32 cells can be driven both orthodromically and antidromically by direct entorhinal stimulation.
33          Only bursting cells could be driven antidromically by entorhinal stimulation.
34 triatal axonal field, neurons were activated antidromically by stimulating their terminal fields in t
35 ynaptic weights in subsets of neurons firing antidromically during SPW-Rs might contribute to memory
36 nal axon terminals as revealed by changes in antidromically evoked cortical potentials, and (2) chang
37 n the mitral cells are all form the ON, this antidromically evoked EPSP may reflect self-excitation o
38 monkeys, whole-cell patch recording revealed antidromically evoked excitatory PSCs that were four tim
39 me Pre-I but none of the E neurones could be antidromically excited from the C(3)-C(4) level of the s
40 ponses to VLF stimulation could be activated antidromically from the VLF, with latencies of less than
41 s, we studied BPAPs generated spontaneously, antidromically (from corticotectal neurons), or via inte
42 x of an awake behaving monkey; 39 cells were antidromically identified as pyramidal tract neurones (P
43                              Some cells were antidromically identified as pyramidal tract neurons (PT
44 lections that distinguish them from adjacent antidromically identified cells.
45 s in primary somatosensory cortex, including antidromically identified corticothalamic cells; similar
46                We compared the properties of antidromically identified CSNs with those of antidromica
47 to probe subthreshold response properties of antidromically identified CT neurons in the rat whisker/
48 onally biased reward outcomes, we found that antidromically identified LHb-projecting neurons were di
49 ion within old and new M1 and area 3a on 135 antidromically identified motoneurons projecting to the
50 antidromically identified CSNs with those of antidromically identified neurons that project via the c
51 Moreover, the patterns of activity evoked in antidromically identified nigro-collicular neurons indic
52  and pharmacological effects of muscarine on antidromically identified septohippocampal neurons (SHNs
53 , whole-cell patch recordings were made from antidromically identified SPNs of immature (12-16-day-ol
54 tion intracellular recordings were made from antidromically identified sympathetic preganglionic neur
55               We describe two populations of antidromically identified trigeminothalamic tract (VTT)
56 ed by studying the extracellular activity of antidromically-identified lamina 5b pyramidal-tract type
57 vity when spikes were evoked synaptically or antidromically in the transverse slice preparation.
58           In addition, four NST neurons were antidromically invaded from the ipsilateral VPMpc.
59  do not change their identity when activated antidromically or orthodromically; (2) the outputs of th
60 of dorsal root reflexes that are transmitted antidromically out to the periphery and these signals ca
61 e to the generation of terminal spikes which antidromically promote bursting in the thalamus.
62  initiation can trigger action potentials to antidromically propagate to the soma in retrograde signa
63 us suprathreshold depolarizations as well as antidromically propagating action potentials ectopically
64 n the rat, eleven of the fifty-four C fibres antidromically stimulated had vasodilator actions.
65 Recent evidence indicates that accumbens DBS antidromically stimulates axon terminals, which ultimate
66 pagates orthodromically toward the soma (and antidromically to more distal regions of the dendrite) a
67  in the distal region of axons and propagate antidromically to the cell body.
68 imately 1 cm away from the STG, and traveled antidromically to the neuropil and orthodromically to th

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