ライフサイエンスコーパス: amygdaloid nucleus

1 us, and the dorsolateral part of the lateral amygdaloid nucleus.

2 is remarkably similar to that of the medial amygdaloid nucleus.

3 ed to be a possible homologue of the central amygdaloid nucleus.

4 is theorized to be homologous to the medial amygdaloid nucleus.

5 ield CA1 and mainly targeted the basolateral amygdaloid nucleus.

6 s-expression by 3.7-times in the basolateral amygdaloid nucleus, 1.2-times in the supraoptic nucleus

7 The anterior cortical amygdaloid nucleus (ACo) is a chemosensory area of the c

8 tly higher in female rats, and in the medial amygdaloid nucleus (Am), GAD(67) mRNA was higher in male

9 c area, several hypothalamic nuclei, central amygdaloid nucleus, amygdalohippocampal area, dorsal per

10 followed by moderate labeling of the medial amygdaloid nucleus, amygdalostriatal zone and caudoputam

11 area of the hypothalamus and also the medial amygdaloid nucleus and CA1 subfield of the hippocampus.

12 l in naked mole-rats include the basolateral amygdaloid nucleus and dentate gyrus, but the septohippo

13 nuclei, hippocampal CA3 region, centromedial amygdaloid nucleus and thalamic paraventricular and reun

14 mporal lobe was associated with the cortical amygdaloid nucleus and the pyramidal cells of the hippoc

15 amygdaloid area, the posterolateral cortical amygdaloid nucleus, and the dorsolateral part of the lat

16 al parvocellular part of the basal accessory amygdaloid nucleus, and the magnocellular part of the ba

17 n neocortex and magnocellular cells in basal amygdaloid nucleus are also intensely CRF(1)-ir.

18 alon: IRP-LI was concentrated in the central amygdaloid nucleus, bed nucleus of stria terminalis and

19 of patients with anxiety and the basolateral amygdaloid nucleus (BLA) in chronic stress mice.

20 Induction in the central amygdaloid nucleus (CeA) and in the bed nucleus of the s

21 The central amygdaloid nucleus (CeA) is a key limbic structure invol

22 al ventricular ridge, PDVR, and dorsolateral amygdaloid nucleus, DLA) subdivisions.

23 at in Cape mole-rats include the basolateral amygdaloid nucleus, hippocampal CA3 subfield, and dentat

24 monkeys (orbitofrontal region) or in the BL amygdaloid nucleus in cats.

25 intaining a central role for the basolateral amygdaloid nucleus in the acquisition and storage of thi

26 specifically, the lateral septum and medial amygdaloid nucleus, indicate greater c-fos mRNA inductio

27 x (PR), and moderate labeling in the lateral amygdaloid nucleus (L).

28 The medial amygdaloid nucleus (Me) is a key nodal point in the neur

29 ing increased c-fos expression in the medial amygdaloid nucleus of both DOM and SUB males as well as

30 iform cortex (Pir), posteriolateral cortical amygdaloid nucleus (PLCo), and the amygdalopiriform tran

31 piriform cortex and posterolateral cortical amygdaloid nucleus (PLCo).

32 ory tubercle, nucleus accumbens, basolateral amygdaloid nucleus, rostroventrolateral medulla and nucl

33 striatal area is more related to the central amygdaloid nucleus than to the striatum.

34 ustrum, bed nucleus of the stria terminalis, amygdaloid nucleus, ventral posterior division of the th

35 ampus and magnocellular cells in basolateral amygdaloid nucleus were also intensely FLNa immunoreacti

36 levels of mRNA of DA receptors in the basal amygdaloid nucleus were measured postmortem in subjects

37 olus vulgaris-leucoagglutinin in the central amygdaloid nucleus were shown to contact cSLR/AAA cholin

38 in the lateral septal nucleus and the medial amygdaloid nucleus, which have numerous Fos-stained nucl