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1 iatal-like projection neurons in the central extended amygdala.
2 nuclei are consistent with the concept of an extended amygdala.
3 CA1, and various nuclei of the amygdala and extended amygdala.
4 nticular gray region, including parts of the extended amygdala.
5 ), the two major subdivisions of the central extended amygdala.
6 ncluding glutamate, to the basal ganglia and extended amygdala.
7 and dynorphin, in the neurocircuitry of the extended amygdala.
8 a terminalis, a key component of the central extended amygdala.
9 previously identified as part of the medial extended amygdala.
10 weeks later in areas of the hypothalamus and extended amygdala.
11 d effects at nearby sites in adjacent LH and extended amygdala.
12 ons have characterized it as a member of the extended amygdala.
13 rminalis (BNST), a CRF-rich component of the extended amygdala.
14 function of extrahypothalamic systems in the extended amygdala.
15 mely low levels of c-fos mRNA in the central extended amygdala.
16 oned fear can inhibit neurons of the central extended amygdala.
17 alis (BSTov), which form part of the central extended amygdala.
18 the distributions of PVs in the striatum and extended amygdala.
19 itional feature distinguishing striatum from extended amygdala.
20 the ventral striatal-pallidal system and the extended amygdala.
21 l striatum, forming an avian analogue of the extended amygdala.
22 ivial amounts in the central division of the extended amygdala.
24 tively induced by morphine withdrawal in the extended amygdala, a group of limbic nuclei that mediate
25 ) and oxytocin (OT) receptor patterns in the extended amygdala, a neural pathway associated with pare
26 e diverse information arising from cortical, extended amygdala and basal forebrain networks to ultima
27 ed amygdala including the central and medial extended amygdala and bed nuclei of the stria terminalis
28 e link between the rostral accumbens and the extended amygdala and demonstrates that dopamine in the
29 y be a characteristic feature distinguishing extended amygdala and its projection areas from striatop
30 Nuclei within the ventromedial hypothalamus, extended amygdala and limbic circuits are known to encod
31 beta-gal expression in the continuum of the extended amygdala and nucleus accumbens, macrostructures
32 nnectivity between ventral striatum (but not extended amygdala) and motor cortex was heightened durin
33 cumbens shell, ventral pallidum, elements of extended amygdala, and lateral septum (but not prefronta
34 callosal cortex, hypothalamus, sublenticular extended amygdala, and left amygdala, even after control
35 urons project to NAc, prefrontal cortex, the extended amygdala, and other forebrain regions but less
36 he medial central nucleus, the sublenticular extended amygdala, and the posterior lateral bed nucleus
37 uitries that comprise the basal ganglia, the extended amygdala, and the prefrontal cortex result in c
38 in-releasing hormone (CRH) system within the extended amygdala appears to mediate stress-induced rela
39 l macrosystems, ventral striatopallidum, and extended amygdala are innervated by substantially coexte
40 ucleus accumbens and central division of the extended amygdala are telencephalic structures that infl
41 Together, this study establishes the medial extended amygdala as a major neural substrate regulating
42 minalis (BNST), a brain relay nucleus in the extended amygdala between cortical/limbic centers, and t
43 cretin transmission throughout hypothalamic, extended amygdala, brainstem, and mesolimbic pathways.
44 ntum produced robust labeling in the central extended amygdala but little in the nucleus accumbens.
45 n motivational centers (ventral striatum and extended amygdala) but also exerted a motivational effec
49 signed to explore the brain sites within the extended amygdala [central nucleus of the amygdala (CeA)
50 a dorsal anterior cingulate-ventral striatum/extended amygdala circuit, such that the "risk allele" d
52 These data reveal that D2R signaling in the extended amygdala constitutes an important checkpoint th
54 Given recent attention to the role of the extended amygdala (EA) in brain reward processes, this s
55 the multisynaptic boundaries of the central extended amygdala extend into BST subnuclei previously i
56 it from understanding alterations in central extended amygdala function in relation to stress-related
57 ites in the anterior half of VP, or in LH or extended amygdala, generally failed to produce any hedon
58 transition" zone between striatopallidum and extended amygdala, had extended amygdala-like afferents
60 ifferent parts of ventral striatopallidum or extended amygdala (homotypic injection pairs) or with on
61 aoptic [SON], and suprachiasmatic [SCN]) and extended amygdala (i.e., bed nucleus of the stria termin
63 ined within the intrinsic connections of the extended amygdala in the caudal sublenticular region and
64 articularly on the basal complex, and on the extended amygdala in the control of states of fear and a
66 bens dopamine neurons and components of the 'extended amygdala' in motivated behavior and reward, it
67 tral viscerolimbic basal ganglia; subpallial extended amygdala including the central and medial exten
68 d in the central and medial divisions of the extended amygdala, including the bed nucleus of stria te
70 nephrine in extrahypothalamic systems in the extended amygdala, including the central nucleus of the
71 e of CRF in extrahypothalamic systems in the extended amygdala, including the central nucleus of the
72 ntral nucleus of the amygdala, sublenticular extended amygdala, interstitial nucleus of the posterior
74 from the parabrachial nuclei to the central extended amygdala, lateral hypothalamus, and ventromedia
75 n striatopallidum and extended amygdala, had extended amygdala-like afferents but produced few double
76 rocessing by the ventral striatopallidal and extended amygdala macrosystems, is reflected in a corres
77 strate that opiate receptors in parts of the extended amygdala may be responsible for the reinforcing
78 pothesis that D-1 dopamine receptors in the 'extended amygdala' may play a significant role in cocain
79 of the amygdala, together referred to as the extended amygdala, may play a role in opiate dependence.
80 ic connections within the central and medial extended amygdala, monosynaptic and transneuronal viral
81 ctures making up the central division of the extended amygdala occurred following injections that inv
83 in signal were observed in the sublenticular extended amygdala of the basal forebrain (SLEA) and the
85 In this investigation, nucleus accumbens and extended amygdala outputs were compared by using retrogr
86 us, multisynaptic circuits within the medial extended amygdala overlap the direct connections making
87 eezing, open-arm avoidance) dependent on the extended amygdala, periaqueductal gray, or septum, all r
89 ved that inhibitory synaptic inputs from the extended amygdala preferentially innervate and suppress
91 injection pairs in the ventral striatum and extended amygdala produced extensive overlap of retrogra
92 indicating that ventral striatopallidum and extended amygdala receive inputs from separate sets of p
93 f the stria terminalis (BST), a component of extended amygdala recently shown to influence feeding vi
94 ions compel a reconsideration of the central extended amygdala's contributions to fear and anxiety an
95 the frontal cortex, ventral striatopallidum, extended amygdala, septum, preoptic region, lateral, par
96 that these two components of the so-called "extended amygdala" serve distinct roles in the encoding
97 Hemodynamic responses in the sublenticular extended amygdala (SLEA) and orbital gyrus tracked the e
98 us of the amygdala (CeA, 77%), sublenticular extended amygdala (SLEA, 86%), interstitial nucleus of t
99 nogamous voles have more OT receptors in the extended amygdala than asocial, nonmonogamous voles.
100 erminalis (BNST), a major subdivision of the extended amygdala that has been proposed to regulate res
101 duncular nucleus, as well as portions of the extended amygdala that included the bed nucleus of the s
102 on of a conceptual macrostructure called the extended amygdala that is recruited during the transitio
103 rs, however, cannot be understood unless the extended amygdala, the basal nucleus of Meynert, and the
105 rvival depends on the ability of the central extended amygdala to rapidly integrate and respond to th
107 obust input from ventral striatopallidum and extended amygdala, whereas RMTg biased inputs arise in s
108 rat PAC increased metabolic activity in the extended amygdala, which is a key substrate of the extra
109 ng factor outside of the hypothalamus in the extended amygdala, which is particularly evident during
110 d less recruitment of the right VS and right-extended amygdala while anticipating responding for gain
111 which a significant number originate in the extended amygdala, while cholinergic neurons outside thi
112 striatum, olfactory tubercles, and areas of extended amygdala with somewhat lighter labeling in the
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