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1 sed selectively in subsets of neurons of the vomeronasal organ.
2 ons for the logic of olfactory coding in the vomeronasal organ.
3 zebrafish olfactory epithelium and the mouse vomeronasal organ.
4 ing TRPC2, a key signalling component of the vomeronasal organ.
5 e developing hyoid bone, pituitary gland and vomeronasal organ.
6 (V2Rs), expressed in the pheromone detecting vomeronasal organ.
7 e OSNs in both the main olfactory system and vomeronasal organ.
8 quire the function of sensory neurons in the vomeronasal organ.
9 type-2 receptor genes (V1Rs and V2Rs) of the vomeronasal organ.
10 cular combinations with specific V2Rs in the vomeronasal organ.
11 y structures, including epithelium, bulb, or vomeronasal organs.
12 ge from vestigial to demonstrably functional vomeronasal organs.
13 lly naive male hamsters after removal of the vomeronasal organs.
14 Here, we considered this question in the vomeronasal organ, a pheromone-detecting epithelium cont
16 cal MHC molecules) proteins expressed in the vomeronasal organ adds to the list of non-traditional ro
17 are also expressed by sensory neurons of the vomeronasal organ, an olfactory structure mediating inna
18 d in subsets of sensory neurons of the mouse vomeronasal organ, an olfactory substructure essential f
19 es, generated by chemosensory input from the vomeronasal organ and (probably) GABA inhibition within
20 s expressed at high levels in the testis and vomeronasal organ and at lower levels in selected other
21 d the pheromone-sensing neurons of the mouse vomeronasal organ and found that responses to dilute uri
22 ed reductions in neuronal cell number in the vomeronasal organ and in the olfactory bulb; the morphol
23 mice, pheromone detection is mediated by the vomeronasal organ and the main olfactory epithelium.
24 stems including the Grueneberg ganglion, the vomeronasal organ, and chemosensory neurons within the m
25 mosensory receptor families expressed in the vomeronasal organ, and contribute to pheromone detection
26 tivates high-affinity sensory neurons in the vomeronasal organ, and downstream limbic neurons in the
27 ng behavior by pheromones is mediated by the vomeronasal organ, and not by the main olfactory epithel
29 The V2R genes are expressed in the mammalian vomeronasal organ, and their products are involved in de
31 in protein and LHRH in cells proximal to the vomeronasal organ anlage that was dependent upon midline
35 f the main olfactory epithelium, but not the vomeronasal organ, causes elevated levels of anxiety.
39 ory olfactory bulb, olfactory epithelial, or vomeronasal organ development at any age in Sey/+ animal
40 rates comprises a main olfactory organ and a vomeronasal organ each containing a morphologically dist
41 encoded by labeled lines at the level of the vomeronasal organ: each pheromonal compound is represent
43 trigeminal and spiral ganglia; olfactory and vomeronasal organ epithelia; postnatal cerebellum; and j
44 ance of sick conspecifics requires an intact vomeronasal organ, expanding the repertoire of biologica
45 ts imply independent evolution of tongue and vomeronasal-organ form, we find evidence for co-variatio
47 king-out selected genes for receptors of the vomeronasal organ has been found to impair specific aspe
48 annel have highlighted the importance of the vomeronasal organ in gender-specific sexual behavior.
53 etween the main olfactory epithelium and the vomeronasal organ in the regulation of sensory neuron de
55 ponents of the main olfactory epithelium and vomeronasal organ involved in pheromone detection; (b) p
57 cent work has shown that transduction in the vomeronasal organ is probably mediated by signalling pat
58 Hence, the neuronal epithelium lining the vomeronasal organ is unique in that it contains stem cel
60 nsduction has come with the cloning from rat vomeronasal organ of a family of putative pheromone rece
66 nasal sensory neurons (VSNs) residing in the vomeronasal organ project axons to the accessory olfacto
70 factory system, in which OSNs located in the vomeronasal organ send their axons to glomeruli in the a
71 accessory olfactory bulb and the survival of vomeronasal organ sensory neurons require the expression
72 crovilli of a number of other sensory cells: vomeronasal organ sensory neurons, solitary chemorecepto
73 ccessory olfactory system and a new role for vomeronasal organ signalling in inhibiting sexual behavi
74 late roughly with anatomical observations of vomeronasal organ size and quality; however, no single e
75 is the finding that deleting the gene for a vomeronasal-organ-specific ion channel causes gender bli
76 structures, including the nasal mucosa, the vomeronasal organ, the epithelium of the lung and intest
77 all neurons of the olfactory epithelium, the vomeronasal organ, the septal organ of Masera, and the G
82 nd neurochemically distinct zones within the vomeronasal organ (VNO) and accessory olfactory bulb (AO
83 tages of accessory olfactory processing, the vomeronasal organ (VNO) and accessory olfactory bulb (AO
84 anatomical and molecular architecture of the vomeronasal organ (VNO) and of its synaptic target, the
85 separate organs within the nasal cavity: the vomeronasal organ (VNO) and the main olfactory epitheliu
87 species, detection of pheromone cues by the vomeronasal organ (VNO) at different concentrations can
88 a neuroanatomical pathway that connects the vomeronasal organ (VNO) at the periphery with downstream
94 ported that female mice lacking a functional vomeronasal organ (VNO) displayed male-typical sexual be
98 e present study, we examined the role of the vomeronasal organ (VNO) in estrus induction and pair bon
100 changes; they are perceived primarily by the vomeronasal organ (VNO) in terrestrial vertebrates.
101 sing hormone (GnRH) neurons migrate from the vomeronasal organ (VNO) in the nasal compartment to the
102 pathfinding of vomeronasal neurons from the vomeronasal organ (VNO) in the periphery to select glome
104 eriments were conducted to determine whether vomeronasal organ (VNO) inputs in male mice mediate the
113 of putative pheromone receptors found in the vomeronasal organ (VNO) of mammals and also in the nose
119 em, the G(o)-containing neurons in the basal vomeronasal organ (VNO) project to the posterior accesso
121 y pheromones and detected by neurones in the vomeronasal organ (VNO) to the accessory olfactory bulb
122 sing hormone (LHRH) neurons migrate from the vomeronasal organ (VNO) to the forebrain in all mammals
124 tudy the transduction of chemosignals in the vomeronasal organ (VNO), for which the functional pathwa
125 e discovered in sensory neurons of the mouse vomeronasal organ (VNO), key detectors of pheromones and
126 vive gestation but die at birth, lacking OE, vomeronasal organ (VNO), nasal cavity, forebrain, lower
127 n of volatile odorants, while neurons in the vomeronasal organ (VNO), part of the accessory olfactory
129 f rodents, the olfactory mucosa (OM) and the vomeronasal organ (VNO), unraveled the molecular basis o
141 ecently that a primary function of the mouse vomeronasal organ (VNO)/accessory olfactory system is se
142 in rodents the chemosensory receptors of the vomeronasal organ, which is specialized in the detection
143 s in the developing olfactory epithelium and vomeronasal organ, with both ligand and receptors (CCK-1
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