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1 t most rVRG inspiratory premotor neurons are enkephalinergic.
2 r voluntary wheel running is associated with enkephalinergic activity in the ventral striatum is not
3 ed overlap exists between the populations of enkephalinergic and serotonergic neuronal afferents to t
4 present study was undertaken to determine if enkephalinergic compounds likewise have the ability to n
5 ng a repressor role for AUF1 proteins during enkephalinergic differentiation.
6 he thoracolumbar spinal cord receive a dense enkephalinergic (ENK) innervation from supraspinal sourc
7        This study sought to determine if the enkephalinergic (ENK) innervation of the hypoglossal nuc
8                           Area X was poor in enkephalinergic fibers and perikarya.
9 te mechanical pain by inhibiting dorsal horn enkephalinergic/GABAergic interneurons.
10 ortex exerts a differential influence on the enkephalinergic (indirect pathway) as opposed to the sub
11  all brain regions that provide GABAergic or enkephalinergic input to the rat RVLM.
12 ed brain regions contribute GABAergic and/or enkephalinergic input to the RVLM.
13 d cardiovascular function, likely through an enkephalinergic mechanism.
14                   Since both cholinergic and enkephalinergic nerves are present in the SpL, the inter
15 he hypothesis that under in vivo conditions, enkephalinergic nerves decrease and neurotensinergic ner
16 s located presynaptically on striatopallidal enkephalinergic neurons and by delta opioid receptors lo
17 ection neuron types by different mechanisms, enkephalinergic neurons by the trophic benefit of BDNF,
18  The densely labeled clusters of Fos-labeled enkephalinergic neurons occurred within larger zones con
19 The present study provides a complete map of enkephalinergic neurons within the forebrain and midbrai
20 ficacy of glutamatergic synapses on striatal enkephalinergic neurons.
21  early gene expression in striatal GABAergic enkephalinergic neurons.
22  in altered intrinsic activation of striatal enkephalinergic neurons.
23 ed descending inputs were dual GABAergic and enkephalinergic (opioidergic).
24 come the inhibition to influence selectively enkephalinergic projection neurons in the activated matr
25 bly selective induction of c-Fos and JunB in enkephalinergic projection neurons.
26     Silencing or activation of the dual GABA/enkephalinergic RVM neurons in adult animals substantial
27                     The enhanced survival of enkephalinergic striatal neurons was correlated with the
28 iatum, partly rescued a preferential loss of enkephalinergic striatal neurons, and enhanced substance
29 sal pallidal neurons that receive input from enkephalinergic striatal neurons, as is true of STN.
30 ived neurotrophic factor-TrkB signaling from enkephalinergic striatal targets unexpectedly leads to s
31 ain-derived neurotrophic factor signaling in enkephalinergic striatopallidal neurons is poorly unders
32  suggest that enhanced responsiveness of the enkephalinergic system to alcohol is associated with, an
33 rs in the dorsal and ventral striatopallidal enkephalinergic system using fluorescence immunohistoche
34 anisms that determine the spatial profile of enkephalinergic volume transmission in LC.

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