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1 nge this assumption, showing that completely spinalized adult rats can recover unassisted hindlimb we
2            The same results were obtained in spinalized, anaesthetised animals.
3                                           In spinalized, anaesthetized rabbits morphine depressed the
4                                 After 2.5 h, spinalized and control rats were perfused for immunocyto
5 st describes the tail withdrawal response in spinalized and intact rats by applying pinpoint heat sti
6 to cutaneous forelimb stimulation in normal, spinalized, and exercised spinalized rats.
7                                       In the spinalized animal, responses were primarily away from th
8 Capsaicin injected into the hindpaw in these spinalized animals produced a small depression.
9 s in normal animals, but does induce them in spinalized animals.
10 tivity in normal animals, but enhances it in spinalized animals.
11 the sensitized response to CRD in intact and spinalized animals.
12    Trunk actions are important in adult rats spinalized as neonates (NTX rats) that walk autonomously
13                           We used adult rats spinalized as neonates because some of these animals dev
14 ted stepping when administered to adult rats spinalized as neonates, to identify the optimal dose for
15  spinal cord preparation (anaesthetized rats spinalized at T10-T11 and cauda equina cut).
16 use-dependent plasticity, as demonstrated in spinalized cats following treadmill training.
17 of hindlimb-hindlimb wiping movements of the spinalized frog were examined.
18 rbation was applied were collected from each spinalized frog.
19 and cutaneous stimulation of the hindlimb of spinalized frogs have provided evidence for a modular or
20 ctrode recordings in the spinal cord gray of spinalized frogs, at 400, 800, and 1200 mum depth, at th
21 rons were still less responsive to stress in spinalized preparations following CFS and AFS.
22 euronal responsiveness to UBD was present in spinalized preparations following exposure to CFS but no
23 cordings of L6-S1 DHNs obtained in intact or spinalized preparations.
24                             In decerebrated, spinalized rabbits with no anaesthesia, HU 210 (30 nmol
25                              In anesthetized spinalized rat, electrical stimulation of the nucleus tr
26                             In anaesthetized spinalized rats electrical stimulation of RVLM elevated
27                                              Spinalized rats given shock whenever 1 hind leg is exten
28 lation of NaCN-sensitive sites in the RVL in spinalized rats increased rCBF measured autoradiographic
29 AG by chemical stimulation were preserved in spinalized rats supporting that the evoked CBF responses
30                                              Spinalized rats that receive shock when 1 hind limb is e
31 o evaluate this hypothesis, the authors gave spinalized rats the protein synthesis inhibitor Cyclohex
32 raspinal input because it was not present in spinalized rats.
33 ponse of these cells in normal and exercised spinalized rats.
34 ulation in normal, spinalized, and exercised spinalized rats.
35 regulated spinal motor pattern generation in spinalized Xenopus embryos.

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