ライフサイエンスコーパス: external globus pallidus

1 topeduncular nucleus/substantia nigra and to external globus pallidus.

2 xicity in mice after local infusion into the external globus pallidus.

3 of PV+ neurons in the cortex, striatum, and external globus pallidus.

4 amics were recapitulated in STN, but also in external globus pallidus and striatum.

5 lamic nucleus (STN) neurons and two types of external globus pallidus (GP) neuron inappropriately syn

6 rgic subthalamic nucleus (STN) and GABAergic external globus pallidus (GP) neurons normally exhibit w

7 oscillations are unknown but activity in the external globus pallidus (GP), which forms a candidate p

8 vity in the reciprocally connected GABAergic external globus pallidus (GPe) and glutamatergic subthal

9 vity in the reciprocally connected GABAergic external globus pallidus (GPe) and glutamatergic subthal

10 Reciprocally connected GABAergic external globus pallidus (GPe) and glutamatergic subthal

11 Reciprocally connected GABAergic external globus pallidus (GPe) and glutamatergic subthal

12 etworks in the subthalamic nucleus (STN) and external globus pallidus (GPe) are associated with the o

13 arvalbumin-expressing (PV(+)) neurons in the external globus pallidus (GPe) are critically involved i

14 in dopamine-depleted rats indicate that the external globus pallidus (GPe) contains two main types o

15 The external globus pallidus (GPe) coordinates action-select

16 show that the excitatory STN and inhibitory, external globus pallidus (GPe) form a feedback system th

17 Autonomously firing GABAergic neurons in the external globus pallidus (GPe) form a local synaptic net

18 Neurons in the external globus pallidus (GPe) generate pacemaker activi

19 ANCE STATEMENT Within the basal ganglia, the external globus pallidus (GPe) has long been recognized

20 ional roles of local axon collaterals in the external globus pallidus (GPe) have remained elusive bec

21 stigated whether the manipulation of the DMS-external globus pallidus (GPe) iMSNs circuit alters the

22 igrostriatal dopamine, the striatum, and the external globus pallidus (GPe) in regulating RLS-like mo

23 way cortical excitation and indirect pathway external globus pallidus (GPe) inhibition of the STN are

24 The external globus pallidus (GPe) is a critical node within

25 The external globus pallidus (GPe) is a key contributor to m

26 The external globus pallidus (GPe) is a key nucleus within b

27 Although external globus pallidus (GPe) is critical for action se

28 Within the basal ganglia circuit, the external globus pallidus (GPe) is critically involved in

29 We show how external globus pallidus (GPe) neuron is sensitive to th

30 efined an analogous division of labor in the external globus pallidus (GPe) of Parkinsonian rats, sho

31 The external globus pallidus (GPe) of the basal ganglia has

32 n of distinct neuronal subpopulations in the external globus pallidus (GPe) provides long-lasting the

33 The external globus pallidus (GPe) regulates motor control.

34 basal ganglia from prototypic neurons in the external globus pallidus (GPe) to their target neurons i

35 rstanding of the neuronal composition in the external globus pallidus (GPe) undermines our ability to

36 eneity of the constituent neurons within the external globus pallidus (GPe) was not fully appreciated

37 e suggests that pathological activity of the external globus pallidus (GPe), a nucleus in the basal g

38 ntly increased during all compulsions in the external globus pallidus (GPe), nucleus accumbens, anter

39 Focusing on the mouse external globus pallidus (GPe), we demonstrate that the

40 nd at the highest levels in the striatum and external globus pallidus (GPe).

41 g-range projection target of A2A-SPNs is the external globus pallidus (GPe).

42 trol signals to the striatum mediated by the external globus pallidus (GPe).

43 ) neurons are distinct neuron classes in the external globus pallidus (GPe): they have different topo

44 bumin-expressing neuronal populations in the external globus pallidus (GPe-PV) and their contribution

45 through the internal globus pallidus (GPi), external globus pallidus, motor cortex, thalamus, or cer

46 Furthermore, we reveal that hyperactivity of external globus pallidus neurons and excessive inhibitio

47 Downstream prototypic parvalbumin-expressing external globus pallidus (PV(+) GPe) neurons discharged

48 tiation of GPi from the internal capsule and external globus pallidus, respectively.

49 nd non-cholinergic projection neurons in the external globus pallidus, suggesting a potential source

50 he newly discovered feedback projection from external globus pallidus to striatum is crucial for inhi

51 mputational model of subthalamic nucleus and external globus pallidus, we extend the concept of adapt

52 rate into an aggregate representation in the external globus pallidus, which could broadcast updates