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1 xicity in mice after local infusion into the external globus pallidus.
2 topeduncular nucleus/substantia nigra and to external globus pallidus.
3 lamic nucleus (STN) neurons and two types of external globus pallidus (GP) neuron inappropriately syn
4 rgic subthalamic nucleus (STN) and GABAergic external globus pallidus (GP) neurons normally exhibit w
5 oscillations are unknown but activity in the external globus pallidus (GP), which forms a candidate p
6 vity in the reciprocally connected GABAergic external globus pallidus (GPe) and glutamatergic subthal
7 vity in the reciprocally connected GABAergic external globus pallidus (GPe) and glutamatergic subthal
8 etworks in the subthalamic nucleus (STN) and external globus pallidus (GPe) are associated with the o
9 in dopamine-depleted rats indicate that the external globus pallidus (GPe) contains two main types o
10 show that the excitatory STN and inhibitory, external globus pallidus (GPe) form a feedback system th
12 igrostriatal dopamine, the striatum, and the external globus pallidus (GPe) in regulating RLS-like mo
13 way cortical excitation and indirect pathway external globus pallidus (GPe) inhibition of the STN are
17 efined an analogous division of labor in the external globus pallidus (GPe) of Parkinsonian rats, sho
18 eneity of the constituent neurons within the external globus pallidus (GPe) was not fully appreciated
19 e suggests that pathological activity of the external globus pallidus (GPe), a nucleus in the basal g
22 through the internal globus pallidus (GPi), external globus pallidus, motor cortex, thalamus, or cer
24 he newly discovered feedback projection from external globus pallidus to striatum is crucial for inhi
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