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1 triatum, medial neostriatum, medial LPO, and archistriatum.
2  that projected to the robust nucleus of the archistriatum.
3 intermediate archistriatum into the anterior archistriatum.
4  and the volume of the robust nucleus of the archistriatum.
5 ers between these two divisions of the chick archistriatum.
6 nterior neostriatum, and subdivisions of the archistriatum.
7  small region in the forebrain, the anterior archistriatum.
8 ate that the central nucleus of the anterior archistriatum (AAc) is the source of ascending projectio
9 ining in the central nucleus of the anterior archistriatum (AAc) resembled that of surrounding archis
10 d to characterize ITD tuning in the auditory archistriatum (AAr), a subdivision of the forebrain gaze
11 ntal neostriatum (NAs), the ventral anterior archistriatum (AAv), the medial archistriatum (Am) and t
12 t to a region adjacent to RA known as dorsal archistriatum (Ad).
13 ral anterior archistriatum (AAv), the medial archistriatum (Am) and the medial HV.
14  limbic archistriatum includes the posterior archistriatum and extends rostrally through the ventral
15 t input to DMP originating in regions of the archistriatum and hypothalamus.
16 o DMP were distributed throughout the dorsal archistriatum and included the area that receives a proj
17 comprises the dorsal intermediate and medial archistriatum and largely gives rise to specific sensory
18 xidase (CO) activity relative to surrounding archistriatum and the underlying shelf, respectively.
19 ntricle, within the tectum, basal forebrain, archistriatum, and caudal neostriatum, and in the hippoc
20 m with its various subdivisions, part of the archistriatum, and probably also the piriform cortex, al
21 than at day 20 and the robust nucleus of the archistriatum, another song nucleus, showed BDNF labelin
22       The data demonstrate that in the avian archistriatum, as in the mammalian frontal cortex, there
23 interconnecting vocal control neurons in the archistriatum, basal ganglia (i.e., lobus parolfactorius
24 ion of the robust nucleus (RA) in the medial archistriatum by P7.
25 results of this study suggest that the chick archistriatum can be divided into two basic divisions ac
26                               The non-limbic archistriatum comprises the dorsal intermediate and medi
27 pallidum contained far less ELI, whereas the archistriatum contained far more than would be expected
28 d adults in area X (delta), robust n. of the archistriatum (delta and mu), and n. intercollicularis (
29 iatum primitivum) and somatomotor (anterior) archistriatum exhibit unique patterns of ELI.
30                    The posterior part of the archistriatum has been renamed the posterior pallial amy
31 rstriatum ventrale, the neostriatum, and the archistriatum have been renamed (respectively) the hyper
32 rons projecting to the robust nucleus of the archistriatum (HVC-RA) were retrogradely labeled with Fl
33 ppocampus, neostriatum, septum, ventromedial archistriatum, hypothalamic regions, dorsal mesencephalo
34                                   The limbic archistriatum includes the posterior archistriatum and e
35                                A part of the archistriatum intermedium and the lateral part of the ne
36 minor, projections to the NFL, TPO, NIL, and archistriatum intermedium.
37 s rostrally through the ventral intermediate archistriatum into the anterior archistriatum.
38 campus, parahippocampal area, hyperstriatum, archistriatum/nucleus (n.) taenia (amygdala), medial par
39                                          The archistriatum of the domestic chick has been implicated
40 ntrolateralis (Avl; comparable to the pigeon archistriatum pars dorsalis) is theorized to be a possib
41                                          The archistriatum pars ventrolateralis (Avl; comparable to t
42 nt targets of HVc, the robust nucleus of the archistriatum (RA) and area X, were smaller ipsilateral
43       In contrast, the robust nucleus of the archistriatum (RA) and the supralaminar area of the fron
44 ical recordings in the robust nucleus of the archistriatum (RA) in adult zebra finch brain slices rev
45 l center (HVC) and the robust nucleus of the archistriatum (RA) in males and females, suggesting a ro
46  to the motor cortical robust nucleus of the archistriatum (RA) is lacking at the onset of song devel
47 ds a projection to the robust nucleus of the archistriatum (RA) of the descending vocal pathway.
48 aration containing the robust nucleus of the archistriatum (RA), a forebrain song control nucleus, an
49 nt targets of HVC, the robust nucleus of the archistriatum (RA), and area X of the parolfactory lobe
50 tical song region, the robust nucleus of the archistriatum (RA), and cause massive RA neuron death in
51 n a compartment of the robust nucleus of the archistriatum (RA), however, this response dwindled as s
52 l center (HVC) and the robust nucleus of the archistriatum (RA), regions involved in song learning an
53 ng nuclei, HVc and the robust nucleus of the archistriatum (RA), the optical disector yielded intergr
54  motor cortex known as robust nucleus of the archistriatum (RA), whereas neurons in lMAN(shell) proje
55 ivity is the forebrain robust nucleus of the archistriatum (RA), which generates stereotyped sequence
56 al center (HVC) to the robust nucleus of the archistriatum (RA), which in turn innervates mesencephal
57  the song nucleus, the robust nucleus of the archistriatum (RA).
58 f the striatum and the robust nucleus of the archistriatum (RA).
59  "cup" adjacent to the robust nucleus of the archistriatum (RA).
60 e proper name) and the robust nucleus of the archistriatum (RA).
61 g-control nucleus, the robust nucleus of the archistriatum (RA).
62 Gold injections in the robust nucleus of the archistriatum (RA); 7 days later, a few such cells could
63 gh vocal center [HVc], robust nucleus of the archistriatum [RA], and Area X) were largest, T was high
64  high vocal center (HVC) and to the "cup" of archistriatum rostrodorsal to another song-control nucle
65  dorsal portion of the robust nucleus of the archistriatum, the motor-cortical output of the song con
66 projections from song control regions of the archistriatum to DMP may feed information back into tele
67  of discrete anatomical regions of the chick archistriatum were therefore investigated by iontophores
68 l fields, except for portions of the ventral archistriatum, which exhibited substantially more TH+ fi

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