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1 an (VNO), which transmits information to the accessory olfactory bulb.
2 We additionally observe CB1 expression in accessory olfactory bulb.
3 ur in the main olfactory bulb and one in the accessory olfactory bulb.
4 FXGs were not seen in axons innervating the accessory olfactory bulb.
5 A), traditionally considered a target of the accessory olfactory bulb.
6 sensory epithelium, main olfactory bulb and accessory olfactory bulb.
7 ervate glomeruli in an ectopic domain of the accessory olfactory bulb.
8 r and posterior sub-regions of the mammalian accessory olfactory bulb.
9 oughout the anterior-posterior extent of the accessory olfactory bulb.
10 rons converge onto numerous glomeruli in the accessory olfactory bulb.
11 xons from vomeronasal sensory neurons in the accessory olfactory bulb.
12 ventrally, and another string dorsal to the accessory olfactory bulb.
13 afferent projections from both the main and accessory olfactory bulbs.
14 eurons and the secondary sorting in main and accessory olfactory bulbs.
15 glomeruli, which reside between the main and accessory olfactory bulbs.
16 d fluorescent microspheres into the main and accessory olfactory bulbs.
17 of the dorsal and lateral cortices, and the accessory olfactory bulb; 2) a bilateral projection that
18 ones, we recorded from single neurons in the accessory olfactory bulb, a nucleus that processes phero
20 udied experience-dependent plasticity in the accessory olfactory bulb and found that internal granule
21 scence signal in the glomerular layer of the accessory olfactory bulb and in the vomeronasal nerve.
22 lidation depends on synaptic inputs from the accessory olfactory bulb and on synaptic outputs to the
23 The formation of this sensory map in the accessory olfactory bulb and the survival of vomeronasal
24 s received olfactory synaptic input from the accessory olfactory bulb and, with the exception of Type
25 of both in the pedunculopontine nuclei, the accessory olfactory bulb, and the supraoptic nucleus of
26 responses of mitral cells recorded from the accessory olfactory bulb (AOB) and main olfactory bulb (
27 es vomeronasal information directly from the accessory olfactory bulb (AOB) and main olfactory inform
29 urones in the vomeronasal organ (VNO) to the accessory olfactory bulb (AOB) and thence to other regio
31 in the periphery to select glomeruli in the accessory olfactory bulb (AOB) are not well understood.
32 Ca(2+) signals in vomeronasal inputs to the accessory olfactory bulb (AOB) during peripheral stimula
33 rsting activity in mitral cells of the mouse accessory olfactory bulb (AOB) emerges from interplay be
34 After salient chemosensory encounters, the accessory olfactory bulb (AOB) experiences changes in th
35 zones within the vomeronasal organ (VNO) and accessory olfactory bulb (AOB) have been identified that
36 ty and an increase in the amount of incoming accessory olfactory bulb (AOB) inputs, as confirmed by e
37 ation on neurotransmitter (NT) expression in accessory olfactory bulb (AOB) interneurons during devel
38 extent of the main olfactory bulb (MOB) and accessory olfactory bulb (AOB) involvement in the discri
39 sing interneurons.SIGNIFICANCE STATEMENT The accessory olfactory bulb (AOB) is a site of experience-d
40 between the mitral and granule cells in the accessory olfactory bulb (AOB) is postulated to play a k
41 nsory information.SIGNIFICANCE STATEMENT The accessory olfactory bulb (AOB) is the first central stag
42 ANCE STATEMENT Information processing in the accessory olfactory bulb (AOB) plays a central role in c
46 We examined local circuit changes in the accessory olfactory bulb (AOB) using targeted ex vivo re
47 ession of mGluRs is particularly high in the accessory olfactory bulb (AOB), a CNS structure critical
48 he first brain relay of the VNS, namely, the accessory olfactory bulb (AOB), change during the cycle.
49 The first dedicated circuit in the AOS, the accessory olfactory bulb (AOB), exhibits cellular and ne
50 organ (VNO) and of its synaptic target, the accessory olfactory bulb (AOB), have suggested that uniq
51 Mitral cells, the principal cells of the accessory olfactory bulb (AOB), receive monosynaptic inp
54 n the vomeronasal organ project axons to the accessory olfactory bulb (AOB), where they form synapses
55 ronasal organ (VNO) project to the posterior accessory olfactory bulb (AOB), whereas more apically lo
56 t central processing stage of the VNS is the accessory olfactory bulb (AOB), which sends information
69 aneously the responses in the main (MOB) and accessory olfactory bulbs (AOB) to odors and pheromones.
71 ssing G(o) and those expressing G(i2) in the accessory olfactory bulb are more clearly separated, in
72 n (LTD) after theta burst stimulation of the accessory olfactory bulb, but not the main accessory bul
74 rvating the main olfactory bulb, but not the accessory olfactory bulb, contained the FXG-associated m
75 ng in glomeruli in the rostral region of the accessory olfactory bulb express G(i2), whereas those pr
76 mating activity in the granule layer of the accessory olfactory bulb (gr-AOB), the bed nucleus of th
77 from the anterior and posterior sub-regions accessory olfactory bulb in mice, as has been reported t
78 mRNA was observed in neurons of the main and accessory olfactory bulbs; in the anterior olfactory nuc
79 tic drive are key elements in organizing the accessory olfactory bulb into functional microcircuits,
80 ynchronized microcircuits that subdivide the accessory olfactory bulb into segregated functional clus
82 ell dendrites, and we show that dendrites of accessory olfactory bulb mitral cells support action pot
83 ns of spontaneous neuronal activity in mouse accessory olfactory bulb mitral cells, the direct neural
84 We show for the first time that some rodent accessory olfactory bulb mitral cells-the direct link be
85 anatomically distinct regions, the main and accessory olfactory bulbs (MOB and AOB), which receive e
86 le-unit electrophysiological recordings from accessory olfactory bulb neurons in ex vivo preparations
87 owed electrophysiological recording from the accessory olfactory bulb of an anesthetized mouse during
90 activity, indeed, reflect the idle state of accessory olfactory bulb output in awake male and female
91 erally connected inhibitory circuitry in the accessory olfactory bulb plays an important role in shap
92 he anterior and posterior sub-regions of the accessory olfactory bulb project to both the medial and
95 tion, we observe individual glomeruli in the accessory olfactory bulb that receive input from more th
98 nt projections to the NS arise solely in the accessory olfactory bulb, the nucleus of the accessory o
99 t, the MA, which receives afferents from the accessory olfactory bulb, the rostroventral lateral cort
100 lei, and granule cell layers of the main and accessory olfactory bulbs, the cerebellum, and the retro
101 Labeled lines might be transferred to the accessory olfactory bulb through convergent connections.
102 ically determined circuit-extending from the accessory olfactory bulb to the posterior medial amygdal
103 nar organization of the deeper layers of the accessory olfactory bulb was indistinct, perhaps as a co
104 g of vomeronasal sensory neuron axons in the accessory olfactory bulb was more uniform for the two le
105 ing in an excess number of LHRH cells in the accessory olfactory bulb, was observed in the NCAM-180 m