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1 A), traditionally considered a target of the accessory olfactory bulb.
2 ur in the main olfactory bulb and one in the accessory olfactory bulb.
3 FXGs were not seen in axons innervating the accessory olfactory bulb.
4 sensory epithelium, main olfactory bulb and accessory olfactory bulb.
5 ervate glomeruli in an ectopic domain of the accessory olfactory bulb.
6 r and posterior sub-regions of the mammalian accessory olfactory bulb.
7 oughout the anterior-posterior extent of the accessory olfactory bulb.
8 rons converge onto numerous glomeruli in the accessory olfactory bulb.
9 xons from vomeronasal sensory neurons in the accessory olfactory bulb.
10 ventrally, and another string dorsal to the accessory olfactory bulb.
11 afferent projections from both the main and accessory olfactory bulbs.
12 eurons and the secondary sorting in main and accessory olfactory bulbs.
13 glomeruli, which reside between the main and accessory olfactory bulbs.
14 d fluorescent microspheres into the main and accessory olfactory bulbs.
15 of the dorsal and lateral cortices, and the accessory olfactory bulb; 2) a bilateral projection that
16 ones, we recorded from single neurons in the accessory olfactory bulb, a nucleus that processes phero
18 scence signal in the glomerular layer of the accessory olfactory bulb and in the vomeronasal nerve.
19 The formation of this sensory map in the accessory olfactory bulb and the survival of vomeronasal
20 s received olfactory synaptic input from the accessory olfactory bulb and, with the exception of Type
21 of both in the pedunculopontine nuclei, the accessory olfactory bulb, and the supraoptic nucleus of
22 responses of mitral cells recorded from the accessory olfactory bulb (AOB) and main olfactory bulb (
23 es vomeronasal information directly from the accessory olfactory bulb (AOB) and main olfactory inform
24 urones in the vomeronasal organ (VNO) to the accessory olfactory bulb (AOB) and thence to other regio
26 in the periphery to select glomeruli in the accessory olfactory bulb (AOB) are not well understood.
27 Ca(2+) signals in vomeronasal inputs to the accessory olfactory bulb (AOB) during peripheral stimula
28 rsting activity in mitral cells of the mouse accessory olfactory bulb (AOB) emerges from interplay be
29 After salient chemosensory encounters, the accessory olfactory bulb (AOB) experiences changes in th
30 zones within the vomeronasal organ (VNO) and accessory olfactory bulb (AOB) have been identified that
31 ation on neurotransmitter (NT) expression in accessory olfactory bulb (AOB) interneurons during devel
32 extent of the main olfactory bulb (MOB) and accessory olfactory bulb (AOB) involvement in the discri
33 sing interneurons.SIGNIFICANCE STATEMENT The accessory olfactory bulb (AOB) is a site of experience-d
34 between the mitral and granule cells in the accessory olfactory bulb (AOB) is postulated to play a k
38 We examined local circuit changes in the accessory olfactory bulb (AOB) using targeted ex vivo re
39 ession of mGluRs is particularly high in the accessory olfactory bulb (AOB), a CNS structure critical
40 organ (VNO) and of its synaptic target, the accessory olfactory bulb (AOB), have suggested that uniq
41 Mitral cells, the principal cells of the accessory olfactory bulb (AOB), receive monosynaptic inp
43 n the vomeronasal organ project axons to the accessory olfactory bulb (AOB), where they form synapses
44 ronasal organ (VNO) project to the posterior accessory olfactory bulb (AOB), whereas more apically lo
55 aneously the responses in the main (MOB) and accessory olfactory bulbs (AOB) to odors and pheromones.
57 ssing G(o) and those expressing G(i2) in the accessory olfactory bulb are more clearly separated, in
58 n (LTD) after theta burst stimulation of the accessory olfactory bulb, but not the main accessory bul
59 rvating the main olfactory bulb, but not the accessory olfactory bulb, contained the FXG-associated m
60 ng in glomeruli in the rostral region of the accessory olfactory bulb express G(i2), whereas those pr
61 mating activity in the granule layer of the accessory olfactory bulb (gr-AOB), the bed nucleus of th
62 from the anterior and posterior sub-regions accessory olfactory bulb in mice, as has been reported t
63 mRNA was observed in neurons of the main and accessory olfactory bulbs; in the anterior olfactory nuc
65 ell dendrites, and we show that dendrites of accessory olfactory bulb mitral cells support action pot
66 ns of spontaneous neuronal activity in mouse accessory olfactory bulb mitral cells, the direct neural
67 We show for the first time that some rodent accessory olfactory bulb mitral cells-the direct link be
68 anatomically distinct regions, the main and accessory olfactory bulbs (MOB and AOB), which receive e
69 le-unit electrophysiological recordings from accessory olfactory bulb neurons in ex vivo preparations
70 owed electrophysiological recording from the accessory olfactory bulb of an anesthetized mouse during
73 erally connected inhibitory circuitry in the accessory olfactory bulb plays an important role in shap
74 he anterior and posterior sub-regions of the accessory olfactory bulb project to both the medial and
77 tion, we observe individual glomeruli in the accessory olfactory bulb that receive input from more th
78 nt projections to the NS arise solely in the accessory olfactory bulb, the nucleus of the accessory o
79 t, the MA, which receives afferents from the accessory olfactory bulb, the rostroventral lateral cort
80 lei, and granule cell layers of the main and accessory olfactory bulbs, the cerebellum, and the retro
81 Labeled lines might be transferred to the accessory olfactory bulb through convergent connections.
82 g of vomeronasal sensory neuron axons in the accessory olfactory bulb was more uniform for the two le
83 ing in an excess number of LHRH cells in the accessory olfactory bulb, was observed in the NCAM-180 m
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