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1 nal mechanosensory and motor center, and the protocerebrum.
2 ginating from the anterior brain region, the protocerebrum.
3 y to neurons located in the posterior medial protocerebrum.
4 he adjacent lateral complex and the superior protocerebrum.
5 ral horn, and the posterior superior lateral protocerebrum.
6 shroom body (MB) and axons into the inferior protocerebrum.
7 t to discrete optic glomeruli in the lateral protocerebrum.
8 3 linked the bilateral auditory areas in the protocerebrum.
9 r clock cell differentiates in the posterior protocerebrum.
10 (MB) calyx and the lateral horn (LH) in the protocerebrum.
11 rge LNs then migrate to new positions in the protocerebrum.
12 li that occupy a major volume of the lateral protocerebrum.
13 rvate the ispsilateral AL and project to the protocerebrum.
14 re innervated at an anterior position on the protocerebrum.
15 riginate from processes that arborize in the protocerebrum.
16 ma-lobe of the mushroom body and the lateral protocerebrum.
17 us and a frontal appendage innervated by the protocerebrum.
18 eruli, optic neuropils, and neuropils of the protocerebrum.
19 very different patterns of projection in the protocerebrum.
20 argely nonoverlapping regions of the lateral protocerebrum.
21 inalis and hemiellipsoid body in the lateral protocerebrum.
22 gives rise to both the visual system and the protocerebrum.
23 before projecting to neuropil regions in the protocerebrum.
24 esses generally ascend to other areas of the protocerebrum.
25 rum/protocerebrum boundary and the posterior protocerebrum.
26 ns that lead from the mushroom body into the protocerebrum.
27 ensory processing) and the posterior lateral protocerebrum, a region we now define as a major site of
28 be efferent neurons terminate in the lateral protocerebrum among the endings of antennal lobe project
29 n a domain that includes a large part of the protocerebrum and a smaller part of the adjacent deutero
30 s are found in regions of the dorsal lateral protocerebrum and abdominal ganglion compared to wild-ty
31 e processes in the dorsomedial region of the protocerebrum and extensive neuronal branches with blebb
32 s extensively supplied by afferents from the protocerebrum and gives rise to a distinctive class of e
33 he optic lobes, circumscribed regions of the protocerebrum and the central complex, particularly the
35 al elements, one connecting with the lateral protocerebrum and the other that exits the optic lobes t
36 urons at the level of the lobula and lateral protocerebrum and with respect to the evolutionary impli
37 tract to the lateral horn of the ipsilateral protocerebrum and, collaterally, to the calyces of the m
39 MdCrz-producing neurons in the dorso-lateral protocerebrum, and eight pairs of bi-lateral neurons in
40 no appendage targets the first ganglion, the protocerebrum, and the corresponding segmental identity
41 true appendage shown to be innervated by the protocerebrum, and thus pycnogonid chelifores are not po
42 We found that most of these areas in the protocerebrum are connected with the AL through multiple
44 L-neurons that project to the contralateral protocerebrum are those that have their dendritic branch
45 M, we identified the ASM cells in the medial protocerebrum as the wake-promoting octopaminergic cells
46 ron with dendrites in an area of the lateral protocerebrum associated with motion-sensitive outputs f
47 the cricket brain occurs within the anterior protocerebrum at the first stage of auditory processing.
48 ly two large clusters at the deuterocerebrum/protocerebrum boundary and the posterior protocerebrum.
51 ctive (5HT-ir) neuron that projects into the protocerebrum, crosses the posterior midline, and innerv
53 cerebralis (group 2), in the superior median protocerebrum (group 3), and in the lateral protocerebru
55 ls in the optic lobe (group 5) and posterior protocerebrum (group 6) were stained only in P. american
56 ) and hemiellipsoid body (HB) in the lateral protocerebrum (higher order center) by a large populatio
57 ppression and projected to the ventrolateral protocerebrum, implying direct communication of chemosen
58 t of neuropils located on the midline of the protocerebrum in several arthropods and has been implica
59 caused by mutations that severely reduce the protocerebrum, including tailless (tll), suggesting that
61 n the fly Neobellieria bullata, the superior protocerebrum is composed of at least five clearly defin
62 Cobalt injections reveal that the superior protocerebrum is richly supplied with local interneurons
63 rconnecting the AMMC, inferior ventrolateral protocerebrum (IVLP), and ventrolateral protocerebrum (V
64 axons to neurons in the lateral horn of the protocerebrum (LHNs) and to Kenyon cells (KCs) in the mu
65 rthermore, areas such as the superior medial protocerebrum now appear to receive olfactory output bot
68 sociated with optic glomeruli in the lateral protocerebrum of the brain of the blowfly Phaenicia seri
69 ctrophysiological recordings from the medial protocerebrum of wild-type flies showed that METH ingest
70 ropils characterize the first brain segment (protocerebrum) of mandibulate and chelicerate arthropods
72 adjacent glomeruli in the Proximal-Antennal-Protocerebrum (PAP) forming a thermotopic map in the bra
75 rtship hearing via third-order ventrolateral protocerebrum Projection Neuron 1 (vPN1) neurons and fou
76 cells supplying the central complex from the protocerebrum propose that such neurons play key roles i
77 plex, and two large 5-HTi processes from the protocerebrum ramify in the medulla and lamina, where th
79 citatory and some inhibitory, in the lateral protocerebrum regulates courtship initiation in Drosophi
80 ned aversion project to the superior lateral protocerebrum (SLP) and convey taste information to mush
81 ivity in the anterior of the superior medial protocerebrum (SMPa) is also transiently and cumulativel
82 ecting the central complex with areas of the protocerebrum suggest that some classes of inputs into t
83 ctivates a sexually dimorphic circuit in the protocerebrum suggests a mechanism by which a single phe
84 dition, a few large 5-HTi processes from the protocerebrum supply the lobula complex, and two large 5
85 a cluster of cells in the posterior lateral protocerebrum that exerts reciprocal effects on the init
86 ring-like branching pattern in the anterior protocerebrum that overlapped with the axonal arborizati
87 sol cells) within a structure in the lateral protocerebrum, the hemiellipsoid body, which is located
88 ennal lobe glomeruli, regions of the lateral protocerebrum, the mushroom body calyces, and the lobula
89 of the main neuropil regions of the lateral protocerebrum: the medulla terminalis and the hemiellips
91 on to conveying olfactory information to the protocerebrum, uniglomerular projection neurons in the a
94 cells, slightly more anterior in the lateral protocerebrum, was found to inhibit courtship when its a
95 s relayed by efferent neurons to the lateral protocerebrum where it is integrated with information ab
96 neuropil structures in the eyestalks lateral protocerebrum, with respect to the optical pathways orig
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