ライフサイエンスコーパス: olfactory cortex

1 in independent subnetworks of neurons in the olfactory cortex.

2 itic inputs with coincidence excitation from olfactory cortex.

3 so present in projections from the OB to the olfactory cortex.

4 ty of odor signals that are delivered to the olfactory cortex.

5 factory neuroepithelium, olfactory bulb, and olfactory cortex.

6 stantially enhanced in the limbic system and olfactory cortex.

7 ted through the axons of bulb neurons to the olfactory cortex.

8 n adult Rana pipiens induces a projection to olfactory cortex.

9 onjugated to horseradish peroxidase into the olfactory cortex.

10 entral relay before being transferred to the olfactory cortex.

11 te to the olfactory bulb, and migrate to the olfactory cortex.

12 etween the bilateral OFC and between the OFC-olfactory cortex.

13 OM cells) contribute to odor coding in mouse olfactory cortex.

14 olfactory epithelium and relays this to the olfactory cortex.

15 ape processing of sensory information in the olfactory cortex.

16 he telencephalic area Dp, the homolog of the olfactory cortex.

17 ry processing occurs at the level of primary olfactory cortex.

18 ells and cortical neurons in slices of mouse olfactory cortex.

19 amic inhibition in space and time within the olfactory cortex.

20 en shown to depend on synaptic adaptation in olfactory cortex.

21 s unclear how this map is represented in the olfactory cortex.

22 c mechanisms shaping odor representations in olfactory cortex.

23 and fate decisions to generate neocortex or olfactory cortex.

24 ation in long-term functional changes within olfactory cortex.

25 olfactory bulb, and hence shape signaling to olfactory cortex.

26 result of reduced plasticity in the primary olfactory cortex.

27 to be combined in individual neurons in the olfactory cortex.

28 to determine how odor identity is encoded in olfactory cortex.

29 that odor coding is broad and distributed in olfactory cortex.

30 ates NMDA receptors at primary inputs to the olfactory cortex.

31 of the adult mouse hippocampus and accessory olfactory cortex.

32 rom piriform cortex, the traditional primary olfactory cortex.

33 ory transmission in pyramidal neurons of rat olfactory cortex.

34 he original engram are preserved in unimodal olfactory cortex.

35 ume loss was most severe in the amygdala and olfactory cortex (82-83% of controls), especially the ca

36 ed functional lateralization in both primary olfactory cortex - a region critical for odor memory and

37 apoptotic death of pyramidal neurons in rat olfactory cortex after total bulbectomy.

38 ceptor to the olfactory bulb and then to the olfactory cortex, allowing visualization of cortical neu

39 e neuron and volume loss in the amygdala and olfactory cortex, although the patterns and extent of lo

40 dor convergence occurs in posterior piriform olfactory cortex and calls for a reformulation of classi

41 rmality in extrahippocampal divisions of the olfactory cortex and cortical and subcortical structures

42 n the thalamus, receiving strong inputs from olfactory cortex and having reciprocal connections with

43 cortex (PCX) is the largest component of the olfactory cortex and is hypothesized to be the locus of

44 performing sequential developmental roles in olfactory cortex and neocortex.

45 t inputs to the hippocampus from the primary olfactory cortex and the general expansion of telencepha

46 gion that in other vertebrates gives rise to olfactory cortex and, when present, to other components

47 sses in the olfactory bulb, olfactory nerve, olfactory cortex, and nervus terminalis located on the a

48 wed significant volume loss in the amygdala, olfactory cortex, and septal region, but others displaye

49 Amygdala, olfactory cortex, and septum occasionally displayed earl

50 was identified superficially, dorsal to the olfactory cortex, and was subsequently covered by the Nr

51 were studied in slices of anterior piriform (olfactory) cortex, and Schaffer-commissural synapses wer

52 her-level association functions derived from olfactory cortex; and human cortical evolution was enhan

53 ergic feedback selectively from the anterior olfactory cortex (AOC) to the OB.

54 egration of sensory information in mammalian olfactory cortex are unclear.

55 nizes electrical activity in human piriform (olfactory) cortex, as well as in limbic-related brain ar

56 interneurons before being transmitted to the olfactory cortex by mitral and tufted (M/T) cells.

57 information processing may occur within the olfactory cortex, direct electrophysiological evidence f

58 the septum, dorsomedial thalamus, amygdala, olfactory cortex, dorsal and ventral hippocampus, substa

59 for the entrainment of slow oscillations in olfactory cortex during ketamine-xylazine anesthesia.

60 evidence of sensory-specific reactivation of olfactory cortex during remembering.

61 These results suggest that SWS replay in the olfactory cortex enhances memory consolidation, and that

62 Progenitors did not generate ectopic olfactory cortex following Lhx2 deletion at E11.5.

63 ncluding six-layer neocortex and three-layer olfactory cortex, generated by telencephalic progenitors

64 calretinin (CR) were found in the neocortex, olfactory cortex, hippocampus, and amygdala, these neuro

65 noreactivity were observed in the neocortex, olfactory cortex, hippocampus, and amygdala.

66 c operations across the serial stages of the olfactory cortex-hippocampus network.

67 In olfactory cortex, however, pyramidal cells receive direc

68 Here we identify a specific area of the olfactory cortex in mice that induces stress hormone res

69 that is enriched in hippocampus and primary olfactory cortex in the adult mouse brain.

70 process the signal and then relay it to the olfactory cortex in the brain.

71 Here, we will discuss the role of the olfactory cortex in the recognition, separation and comp

72 es revealed a stereotyped sensory map in the olfactory cortex in which signals from a particular rece

73 In the mouse olfactory cortex, individual odorants are represented by

74 How this map is linked with olfactory cortex is unknown.

75 ory bulb; it may be due to plasticity within olfactory cortex itself.

76 puncta in the dorsolateral prominence of the olfactory cortex may have relevance to the functional or

77 non-topographic projections to and from the olfactory cortex may suggest a flat, non-hierarchical or

78 tiating predictie information; the piriform (olfactory) cortex meanwhile clusters similar and co-occu

79 that "global" inhibition within the primary olfactory cortex might accomplish a similar end.

80 of a greater experimental tractability, the olfactory cortex might prove to be instrumental in uncov

81 uronal types in the hippocampus, cerebellum, olfactory cortex, neocortex, and elsewhere express from

82 of either spherical or rodlike shape in the olfactory cortex, nucleus isthmi, and hypothalamus.

83 hesized to help bind information together in olfactory cortex (OC).

84 allial portions of the FB, equivalent to the olfactory cortex of amniote vertebrates, whereas social

85 e we show that blockade of mGluRs within the olfactory cortex of awake, behaving rats diminishes habi

86 ions of as few as 300 neurons in the primary olfactory cortex of mice suffices for associative learni

87 eruli to third-order neurons (neurons in the olfactory cortex of vertebrates or Kenyon cells in the m

88 lectrical activity of neurons in the primary olfactory cortex on a rapid (<1 s) timescale but leaves

89 ed in KO compared with WT mice in either the olfactory cortex or hippocampus.

90 ent with oxytocin's function in the anterior olfactory cortex, particularly in social cue processing,

91 We speculate that the olfactory cortex plays a key role in tuning the readout

92 at AmPir, a small area comprising <5% of the olfactory cortex, plays a key part in the hormonal compo

93 gen level-dependent (BOLD) signal at primary olfactory cortex (POC) was weaker in AD than in HC subje

94 probe this attentional mechanism in primary olfactory cortex (POC).

95 hitecture, physiology, and plasticity of the olfactory cortex, principally the piriform cortex, will

96 nsiently increased the drive of the anterior olfactory cortex projecting to olfactory bulb interneuro

97 we selectively express channelrhodopsin-2 in olfactory cortex pyramidal cells and show that cortical

98 Olfactory cortex pyramidal cells integrate sensory input

99 postnatal time window at sensory synapses of olfactory cortex pyramidal cells.

100 to generate three-layer cortex, phenocopying olfactory cortex rather than lateral neocortex.

101 fact that multiple structures of the primary olfactory cortex receive projections from the olfactory

102 lly organized retinal projection in the frog olfactory cortex revealed that the temporal retina is th

103 lectrophoresis of DNA purified from lesioned olfactory cortex showed a ladder pattern of fragmentatio

104 by olfactory bulb afferents to the piriform (olfactory) cortex significantly contributes to adaptatio

105 e analysis of paired whole-cell recording in olfactory cortex slices.

106 This coupling between olfactory cortex slow oscillations and respiration may r

107 g evidence for slow- and fast-wave states in olfactory cortex that appear to gate the inflow of infor

108 ime window and is a feature intrinsic to the olfactory cortex that can be explained by the integratio

109 eferences of principal neurons in the OB and olfactory cortex that innervate granule cells (GCs) may

110 In vivo, activation of olfactory cortex that only weakly affects spontaneous M/

111 bulb (OB) receives top-down inputs from the olfactory cortex that produce direct excitation and feed

112 tatory inputs mostly from the regions of the olfactory cortex that project back to the OB.

113 ribe a novel seizure pattern peculiar of the olfactory cortex that resembles focal seizures with low-

114 eveals a sequence of ictogenic events in the olfactory cortex that were never described before in oth

115 found nostril-specific responses in primary olfactory cortex that were predictive of the accuracy of

116 h reinforces the top-down influence from the olfactory cortex to early stages of olfactory informatio

117 papers analyze the features of feedback from olfactory cortex to olfactory bulb.

118 e probed the excitatory network in the mouse olfactory cortex using variance analysis of paired whole

119 information is then transmitted to piriform (olfactory) cortex, via axons of olfactory bulb mitral an

120 to provide evidence of apoptosis; neurons in olfactory cortex were counted by stereology.

121 ibuted subnetworks are weak or absent in the olfactory cortex, whereas a hierarchical excitatory topo

122 all of the pallial amygdala but also to the olfactory cortex, which hitherto was considered to arise

123 In the olfactory cortex, which lacks an obvious columnar struct

124 heterogeneous functional connectivity in the olfactory cortex with a resolution surpassing substantia

125 t cell bodies, were studied in rat piriform (olfactory) cortex with antisera to gamma-aminobutyric ac