ライフサイエンスコーパス: vomeronasal organ

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 quire the function of sensory neurons in the vomeronasal organ.

8 type-2 receptor genes (V1Rs and V2Rs) of the vomeronasal organ.

9 e OSNs in both the main olfactory system and 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 at GnRH(OB) neurons extend neurites into the vomeronasal organ and olfactory epithelium and project t

24 mice, pheromone detection is mediated by the vomeronasal organ and the main olfactory epithelium.

25 stems including the Grueneberg ganglion, the vomeronasal organ, and chemosensory neurons within the m

26 mosensory receptor families expressed in the vomeronasal organ, and contribute to pheromone detection

27 tivates high-affinity sensory neurons in the vomeronasal organ, and downstream limbic neurons in the

28 ng behavior by pheromones is mediated by the vomeronasal organ, and not by the main olfactory epithel

29 Fish do not have a vomeronasal organ, and their olfactory neurons-three dif

30 The V2R genes are expressed in the mammalian vomeronasal organ, and their products are involved in de

31 Cells within the vomeronasal organ anlage that turn on LHRH gene and pept

32 in protein and LHRH in cells proximal to the vomeronasal organ anlage that was dependent upon midline

33 tected in early expressing LHRH cells in the vomeronasal organ anlage.

34 GAD mRNA was dramatically reduced in the OP/vomeronasal organ by E16.5.

35 Snakes deliver odorants to the vomeronasal organ by means of tongue-flicks.

36 f the main olfactory epithelium, but not the vomeronasal organ, causes elevated levels of anxiety.

37 The vomeronasal organ detects chemical cues that trigger sex

38 The mammalian vomeronasal organ detects complex chemical signals that

39 The mammalian vomeronasal organ detects social information about gende

40 ory olfactory bulb, olfactory epithelial, or vomeronasal organ development at any age in Sey/+ animal

41 rates comprises a main olfactory organ and a vomeronasal organ each containing a morphologically dist

42 encoded by labeled lines at the level of the vomeronasal organ: each pheromonal compound is represent

43 The mammalian vomeronasal organ encodes pheromone information about ge

44 trigeminal and spiral ganglia; olfactory and vomeronasal organ epithelia; postnatal cerebellum; and j

45 ance of sick conspecifics requires an intact vomeronasal organ, expanding the repertoire of biologica

46 ts imply independent evolution of tongue and vomeronasal-organ form, we find evidence for co-variatio

47 ring in the pheromone-sensing neurons of the vomeronasal organ from female mouse urine.

48 king-out selected genes for receptors of the vomeronasal organ has been found to impair specific aspe

49 The AOS comprising the peripheral sensory vomeronasal organ has evolved elaborate molecular and ce

50 annel have highlighted the importance of the vomeronasal organ in gender-specific sexual behavior.

51 Growth deficiency of the vomeronasal organ in Heterocephalus may relate to a dimi

52 In light of the unique aspects of the vomeronasal organ in Heterocephalus, comparative studies

53 Electrical stimulation of the vomeronasal organ in male hamsters activated Fos express

54 with pheromonal communication involving the vomeronasal organ in other rodents.

55 etween the main olfactory epithelium and the vomeronasal organ in the regulation of sensory neuron de

56 ingly, no previous studies have examined the vomeronasal organ in this species.

57 ponents of the main olfactory epithelium and vomeronasal organ involved in pheromone detection; (b) p

58 Although the vomeronasal organ is often regarded as only a pheromone

59 cent work has shown that transduction in the vomeronasal organ is probably mediated by signalling pat

60 Hence, the neuronal epithelium lining the vomeronasal organ is unique in that it contains stem cel

61 The morphology of the tongue and the vomeronasal-organs is believed to mirror this dichotomy.

62 nsduction has come with the cloning from rat vomeronasal organ of a family of putative pheromone rece

63 nt-associated proliferation continues in the vomeronasal organ of aged (18-24 months) mice.

64 The vomeronasal organ of mammals is an olfactory sensory str

65 The vomeronasal organ of the accessory olfactory system dete

66 sory neurons in the olfactory epithelium and vomeronasal organ of transgenic mice.

67 Odors detected by the vomeronasal organ or the main olfactory epithelium (MOE)

68 nasal sensory neurons (VSNs) residing in the vomeronasal organ project axons to the accessory olfacto

69 The rodent vomeronasal organ provides a unique system to examine in

70 In sexually naive males, vomeronasal organ removal (VNX), but not main olfactory

71 In males with vomeronasal organs removed (VNX), there was an also an i

72 Males with vomeronasal organs removed and without sexual experience

73 factory system, in which OSNs located in the vomeronasal organ send their axons to glomeruli in the a

74 accessory olfactory bulb and the survival of vomeronasal organ sensory neurons require the expression

75 crovilli of a number of other sensory cells: vomeronasal organ sensory neurons, solitary chemorecepto

76 ccessory olfactory system and a new role for vomeronasal organ signalling in inhibiting sexual behavi

77 late roughly with anatomical observations of vomeronasal organ size and quality; however, no single e

78 is the finding that deleting the gene for a vomeronasal-organ-specific ion channel causes gender bli

79 structures, including the nasal mucosa, the vomeronasal organ, the epithelium of the lung and intest

80 all neurons of the olfactory epithelium, the vomeronasal organ, the septal organ of Masera, and the G

81 cloning efforts have extended studies of the vomeronasal organ to cellular and molecular levels.

82 unravel the functional connectivity from the vomeronasal organ to the hypothalamus.

83 Pheromones are detected by the vomeronasal organ using members of two receptor superfam

84 Because sensory neurons in the vomeronasal organ (VNO) also respond to MHC peptides but

85 nd neurochemically distinct zones within the vomeronasal organ (VNO) and accessory olfactory bulb (AO

86 tages of accessory olfactory processing, the vomeronasal organ (VNO) and accessory olfactory bulb (AO

87 anatomical and molecular architecture of the vomeronasal organ (VNO) and of its synaptic target, the

88 cial and sexual behavior are detected by the vomeronasal organ (VNO) and processed in the accessory o

89 separate organs within the nasal cavity: the vomeronasal organ (VNO) and the main olfactory epitheliu

90 Bipolar sensory neurons within the vomeronasal organ (VNO) are thought to mediate the detec

91 species, detection of pheromone cues by the vomeronasal organ (VNO) at different concentrations can

92 a neuroanatomical pathway that connects the vomeronasal organ (VNO) at the periphery with downstream

93 The epithelium of the mouse vomeronasal organ (VNO) consists of apical and basal lay

94 The sensory epithelium of the vomeronasal organ (VNO) contains primary chemosensory re

95 The vomeronasal organ (VNO) contains two main types of vomer

96 Chemosensory neurons in the vomeronasal organ (VNO) detect pheromones that elicit so

97 In terrestrial vertebrates, the vomeronasal organ (VNO) detects and transduces pheromone

98 The vomeronasal organ (VNO) detects pheromones in many verte

99 ported that female mice lacking a functional vomeronasal organ (VNO) displayed male-typical sexual be

100 The vomeronasal organ (VNO) does not appear to change functi

101 Pheromonal activation of the vomeronasal organ (VNO) elicits genetically preprogramme

102 The vomeronasal organ (VNO) has a key role in mediating the

103 e present study, we examined the role of the vomeronasal organ (VNO) in estrus induction and pair bon

104 ges, and they are perceived primarily by the vomeronasal organ (VNO) in terrestrial vertebrates.

105 changes; they are perceived primarily by the vomeronasal organ (VNO) in terrestrial vertebrates.

106 sing hormone (GnRH) neurons migrate from the vomeronasal organ (VNO) in the nasal compartment to the

107 pathfinding of vomeronasal neurons from the vomeronasal organ (VNO) in the periphery to select glome

108 The volume of the vomeronasal organ (VNO) in the terrestrial salamander Pl

109 eriments were conducted to determine whether vomeronasal organ (VNO) inputs in male mice mediate the

110 urons (GnRH-1ns) migrate from the developing vomeronasal organ (VNO) into the brain asserting control

111 The vomeronasal organ (VNO) is a chemoreceptive organ that i

112 The vomeronasal organ (VNO) is a chemoreceptor organ enclose

113 The vomeronasal organ (VNO) is a chemosensory organ speciali

114 The mammalian vomeronasal organ (VNO) is an accessory olfactory struct

115 The vomeronasal organ (VNO) is essential for intraspecies co

116 transduction in chemosensory neurons of the vomeronasal organ (VNO) is not known.

117 The mouse vomeronasal organ (VNO) is thought to mediate social beh

118 The vomeronasal organ (VNO) mediates detection of pheromones

119 Pheromone detection by the vomeronasal organ (VNO) mediates important social behavi

120 of putative pheromone receptors found in the vomeronasal organ (VNO) of mammals and also in the nose

121 The vomeronasal organ (VNO) of mammals plays an essential ro

122 The vomeronasal organ (VNO) of mammals plays an essential ro

123 The vomeronasal organ (VNO) of terrestrial vertebrates plays

124 The vomeronasal organ (VNO) of the mouse has two neuronal co

125 The mouse vomeronasal organ (VNO) plays a critical role in semioch

126 em, the G(o)-containing neurons in the basal vomeronasal organ (VNO) project to the posterior accesso

127 behaviorally instructive chemical cues, the vomeronasal organ (VNO) remains a poorly characterized m

128 Microvilli of vomeronasal organ (VNO) sensory epithelium receptor cell

129 The vomeronasal organ (VNO) serves as a primary sensory chan

130 y pheromones and detected by neurones in the vomeronasal organ (VNO) to the accessory olfactory bulb

131 sing hormone (LHRH) neurons migrate from the vomeronasal organ (VNO) to the forebrain in all mammals

132 The mammalian vomeronasal organ (VNO), a part of the olfactory system,

133 cted aggression are tightly regulated by the vomeronasal organ (VNO), but how diverse subsets of sens

134 tudy the transduction of chemosignals in the vomeronasal organ (VNO), for which the functional pathwa

135 e discovered in sensory neurons of the mouse vomeronasal organ (VNO), key detectors of pheromones and

136 vive gestation but die at birth, lacking OE, vomeronasal organ (VNO), nasal cavity, forebrain, lower

137 n of volatile odorants, while neurons in the vomeronasal organ (VNO), part of the accessory olfactory

138 In the vomeronasal organ (VNO), receptor neurons with their cel

139 f rodents, the olfactory mucosa (OM) and the vomeronasal organ (VNO), unraveled the molecular basis o

140 The mouse vomeronasal organ (VNO), which detects pheromones and ot

141 are detected by chemosensory neurons of the vomeronasal organ (VNO), which transmits information to

142 y in trp2, a cation channel expressed in the vomeronasal organ (VNO).

143 in the main olfactory epithelium and in the vomeronasal organ (VNO).

144 nasal cavity and the neuroepithelium of the vomeronasal organ (VNO).

145 ons and subsequent stimulus detection by the vomeronasal organ (VNO).

146 within a subsystem of the nasal cavity, the vomeronasal organ (VNO).

147 the main olfactory epithelium (MOE) and the vomeronasal organ (VNO).

148 in terrestrial vertebrates primarily by the vomeronasal organ (VNO).

149 eromone receptors expressed in the mammalian vomeronasal organ (VNO).

150 a separate olfactory epithelium lies in the vomeronasal organ (VNO).

151 are located in the sensory epithelium of the vomeronasal organ (VNO).

152 (MOE) and pheromones are sensed through the vomeronasal organ (VNO).

153 ecently that a primary function of the mouse vomeronasal organ (VNO)/accessory olfactory system is se

154 erated single cell transcriptomic atlases of vomeronasal organs (VNO) from juvenile and adult mice.

155 in rodents the chemosensory receptors of the vomeronasal organ, which is specialized in the detection

156 s in the developing olfactory epithelium and vomeronasal organ, with both ligand and receptors (CCK-1