ライフサイエンスコーパス: central gray

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1 sion of the periaqueductal gray, and pontine central gray.

2 tectum, superior and inferior colliculi, and central gray.

3 ygdala, in a few thalamic nuclei, and in the central gray.

4 osis behavior when infused into the midbrain central gray.

5 ral and dorsal aspects of the periaqueductal central gray.

6 cleus, the median/paramedian nuclei, and the central gray.

7 if any TH-positive neurons were found in the central gray and dorsal raphe.

8 rrounding the locus coeruleus, including the central gray and the dorsal and median raphe nuclei.

9 rostral-linearis, the subcommissural organ, central gray, and in glia surrounding the cerebral aqued

10 ia caudal pontine reticular nucleus, pontine central gray, and MS, reached EC.

11 dopallium and arcopallium, the mesencephalic central gray, and the dorsolateralis anterior (DLL) and

12 isceral nucleus, the cerebellar nucleus, the central gray, and the nucleus of the solitary tract.

13 dian raphe, caudal dorsal raphe, and pontine central gray are major recipients of LHb efferents.

14 dala, lateral amygdala, arcuate nucleus, and central gray area, regardless of group.

15 gyrus, nucleus accumbens shell and core, and central gray area, regardless of whether or not priming

16 terminalis (BNST), lateral habenula (LHAB), central gray (CG), thalamus (THAL), septum (SEPT), and v

17 ith a smaller contribution from the midbrain central gray (CG).

18 enula, inferior colliculus, dorsal raphe and central gray compared to saline.

19 As predicted, DZ infusions into the midbrain central gray did not reduce the reticulospinal-evoked ax

20 us; 3) discrete nuclei of pontomesencephalic central gray (dorsal raphe nucleus, laterodorsal tegment

21 n control in the habenula, dorsal raphe, and central gray following adminstration of 18 microg/kg of

22 ent with the facilitatory effect of midbrain central gray infusions of DZ on the lordosis quotient.

23 acta (substantia nigra), intercollicular n., central gray, locus ceruleus, parabrachial n., ventrolat

24 t concentrations were measured in the dorsal central gray matter (periaqueductal gray), the locus coe

25 centration of postsynaptic DC neurons in the central gray matter of the L6-S1 spinal segments, and an

26 nuclei, the inferior colliculus, the ventral central gray matter, the pontine tegmentum, the amygdala

27 aroxetine binding was present throughout the central gray matter, with relatively homogeneous labelin

28 rain ventral to the cerebral aqueduct in the central gray matter.

29 n the lateral periaqueductal gray and in the central gray nucleus.

30 nigra, nucleus of the posterior commissure, central gray, nucleus of Darkschewitsch, peripeduncular

31 The midline central gray of the pons and nucleus incertus receive in

32 The lateral central gray of the pons receives bilateral input from t

33 formation, basolateral and medial amygdala, central gray, pontine nuclei, interpeduncular nucleus, s

34 n, substantia nigra, ventral tegmental area, central gray, raphe complex, locus coeruleus, multiple b

35 nd interpeduncular nuclei; substantia nigra, central gray; raphe nuclei; parabrachial nuclei; locus c

36 dian raphe, caudal dorsal raphe, and pontine central gray reside in characteristic, but sometimes ove

37 a, IPe, arcuate nucleus of hypothalamus, and central gray substance of midbrain, respectively.

38 n; medial region of the superior colliculus, central gray substance of the midbrain and dorsal raphe

39 l regions of the posterior hypothalamus, the central gray, the cerebellum, the parabrachial nuclei, t

40 he nucleus of Darkschewitsch, the oculomotor central gray, the cuneiform, and the lateral dorsal, ped

41 e zona incerta, the subthalamic nucleus, the central gray, the substantia nigra, the raphe nuclei, th

42 LC; medial GABAergic neurons in the pontine central gray; ventromedial, small GABAergic neurons that

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