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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
15                                          The vomeronasal organ, a sensory structure within the olfact
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
28                           Fish do not have a vomeronasal organ, and their olfactory neurons-three dif
29 The V2R genes are expressed in the mammalian vomeronasal organ, and their products are involved in de
30                             Cells within the vomeronasal organ anlage that turn on LHRH gene and pept
31 in protein and LHRH in cells proximal to the vomeronasal organ anlage that was dependent upon midline
32 tected in early expressing LHRH cells in the vomeronasal organ anlage.
33  GAD mRNA was dramatically reduced in the OP/vomeronasal organ by E16.5.
34               Snakes deliver odorants to the vomeronasal organ by means of tongue-flicks.
35 f the main olfactory epithelium, but not the vomeronasal organ, causes elevated levels of anxiety.
36                                          The vomeronasal organ detects chemical cues that trigger sex
37                                The mammalian vomeronasal organ detects complex chemical signals that
38                                The mammalian vomeronasal organ detects social information about gende
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
42                                The mammalian vomeronasal organ encodes pheromone information about ge
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
46 ring in the pheromone-sensing neurons of the vomeronasal organ from female mouse urine.
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.
49                     Growth deficiency of the vomeronasal organ in Heterocephalus may relate to a dimi
50        In light of the unique aspects of the vomeronasal organ in Heterocephalus, comparative studies
51                Electrical stimulation of the vomeronasal organ in male hamsters activated Fos express
52  with pheromonal communication involving the vomeronasal organ in other rodents.
53 etween the main olfactory epithelium and the vomeronasal organ in the regulation of sensory neuron de
54 ingly, no previous studies have examined the vomeronasal organ in this species.
55 ponents of the main olfactory epithelium and vomeronasal organ involved in pheromone detection; (b) p
56                                 Although the vomeronasal organ is often regarded as only a pheromone
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
59         The morphology of the tongue and the vomeronasal-organs is believed to mirror this dichotomy.
60 nsduction has come with the cloning from rat vomeronasal organ of a family of putative pheromone rece
61 nt-associated proliferation continues in the vomeronasal organ of aged (18-24 months) mice.
62                                          The vomeronasal organ of mammals is an olfactory sensory str
63                                          The vomeronasal organ of the accessory olfactory system dete
64 sory neurons in the olfactory epithelium and vomeronasal organ of transgenic mice.
65                        Odors detected by the vomeronasal organ or the main olfactory epithelium (MOE)
66 nasal sensory neurons (VSNs) residing in the vomeronasal organ project axons to the accessory olfacto
67                     In sexually naive males, vomeronasal organ removal (VNX), but not main olfactory
68                                In males with vomeronasal organs removed (VNX), there was an also an i
69                                   Males with vomeronasal organs removed and without sexual experience
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
78 cloning efforts have extended studies of the vomeronasal organ to cellular and molecular levels.
79 unravel the functional connectivity from the vomeronasal organ to the hypothalamus.
80               Pheromones are detected by the vomeronasal organ using members of two receptor superfam
81               Because sensory neurons in the vomeronasal organ (VNO) also respond to MHC peptides but
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
86           Bipolar sensory neurons within the vomeronasal organ (VNO) are thought to mediate the detec
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
89                  The epithelium of the mouse vomeronasal organ (VNO) consists of apical and basal lay
90                The sensory epithelium of the vomeronasal organ (VNO) contains primary chemosensory re
91                  Chemosensory neurons in the vomeronasal organ (VNO) detect pheromones that elicit so
92              In terrestrial vertebrates, the vomeronasal organ (VNO) detects and transduces pheromone
93                                          The vomeronasal organ (VNO) detects pheromones in many verte
94 ported that female mice lacking a functional vomeronasal organ (VNO) displayed male-typical sexual be
95                                          The vomeronasal organ (VNO) does not appear to change functi
96                 Pheromonal activation of the vomeronasal organ (VNO) elicits genetically preprogramme
97                                          The vomeronasal organ (VNO) has a key role in mediating the
98 e present study, we examined the role of the vomeronasal organ (VNO) in estrus induction and pair bon
99 ges, and they are perceived primarily by the vomeronasal organ (VNO) in terrestrial vertebrates.
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
103                            The volume of the vomeronasal organ (VNO) in the terrestrial salamander Pl
104 eriments were conducted to determine whether vomeronasal organ (VNO) inputs in male mice mediate the
105                                          The vomeronasal organ (VNO) is a chemoreceptive organ that i
106                                          The vomeronasal organ (VNO) is a chemoreceptor organ enclose
107                                          The vomeronasal organ (VNO) is a chemosensory organ speciali
108                                The mammalian vomeronasal organ (VNO) is an accessory olfactory struct
109                                          The vomeronasal organ (VNO) is essential for intraspecies co
110  transduction in chemosensory neurons of the vomeronasal organ (VNO) is not known.
111                                    The mouse vomeronasal organ (VNO) is thought to mediate social beh
112                                          The vomeronasal organ (VNO) mediates detection of pheromones
113 of putative pheromone receptors found in the vomeronasal organ (VNO) of mammals and also in the nose
114                                          The vomeronasal organ (VNO) of mammals plays an essential ro
115                                          The vomeronasal organ (VNO) of mammals plays an essential ro
116                                          The vomeronasal organ (VNO) of terrestrial vertebrates plays
117                                          The vomeronasal organ (VNO) of the mouse has two neuronal co
118                                    The mouse vomeronasal organ (VNO) plays a critical role in semioch
119 em, the G(o)-containing neurons in the basal vomeronasal organ (VNO) project to the posterior accesso
120                                Microvilli of vomeronasal organ (VNO) sensory epithelium receptor cell
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
123                                The mammalian vomeronasal organ (VNO), a part of the olfactory system,
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
128                                       In the vomeronasal organ (VNO), receptor neurons with their cel
129 f rodents, the olfactory mucosa (OM) and the vomeronasal organ (VNO), unraveled the molecular basis o
130                                    The mouse vomeronasal organ (VNO), which detects pheromones and ot
131 y in trp2, a cation channel expressed in the vomeronasal organ (VNO).
132  in the main olfactory epithelium and in the vomeronasal organ (VNO).
133  nasal cavity and the neuroepithelium of the vomeronasal organ (VNO).
134  within a subsystem of the nasal cavity, the vomeronasal organ (VNO).
135  a separate olfactory epithelium lies in the vomeronasal organ (VNO).
136  the main olfactory epithelium (MOE) and the vomeronasal organ (VNO).
137  in terrestrial vertebrates primarily by the vomeronasal organ (VNO).
138 eromone receptors expressed in the mammalian vomeronasal organ (VNO).
139 are located in the sensory epithelium of the vomeronasal organ (VNO).
140  (MOE) and pheromones are sensed through the vomeronasal organ (VNO).
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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