ライフサイエンスコーパス: glomerular layer

1 ion of molecular features represented in the glomerular layer.

2 cteristic spatial pattern of activity in the glomerular layer.

3 2-DG uptake average over the entire analyzed glomerular layer.

4 gal projections that diffusely innervate the glomerular layer.

5 to interneurons of the granule cell layer or glomerular layer.

6 arization that was largely restricted to the glomerular layer.

7 ted by GABAergic synapses formed outside the glomerular layer.

8 al excitatory sensory input contained in the glomerular layer.

9 pe: axon-bearing dopaminergic neurons in the glomerular layer.

10 e bulbar granule cell (GC) layer but not the glomerular layer.

11 tion of SACs evoked robust DA release in the glomerular layer.

12 from olfactory sensory neurons (OSNs) in the glomerular layer.

13 neurons that integrate into the superficial glomerular layer.

14 c inhibition, a third of which arises in the glomerular layer.

15 t also leads to widespread disruption of the glomerular layer.

16 ated, alpha-BGT binding was localized to the glomerular layer.

17 expression in the olfactory nerve and in the glomerular layer.

18 iciency specifically alters formation of the glomerular layer.

19 minal maturation of neurons destined for the glomerular layer.

20 ransmission from second-order neurons in the glomerular layer.

21 ABAergic/nondopaminergic interneurons of the glomerular layer.

22 scattered in the anterior region of the AOB glomerular layer.

23 of glomeruli in the anterior half of the AOB glomerular layer.

24 minimal in the olfactory nerve layer and the glomerular layer.

25 ng axons before entering the neuropil of the glomerular layer.

26 to structure across approximately 80% of the glomerular layer.

27 [(14)C]2-deoxyglucose in the olfactory bulb glomerular layer.

28 ess that extends from the ventricle into the glomerular layer.

29 ylase, is largely confined to neurons in the glomerular layer.

30 and the juxtaglomerular (JG) neurons of the glomerular layer.

31 In previous studies, we mapped glomerular layer 2-deoxyglucose uptake evoked by hundred

32 arger percentage of GABAergic neurons in the glomerular layer (55% of all neurons) than previously re

33 atly in the posterolateral and posteromedial glomerular layer, a finding one should predict, given th

34 albindin-positive cells were detected in the glomerular layer, accompanied by an increase in cells po

35 of GC-D+ neurons form ectopically within the glomerular layer, across wide areas of the main olfactor

36 ncoded in the nervous system, we studied the glomerular-layer activity patterns in the rat olfactory

37 the effects of functional group position on glomerular-layer activity patterns.

38 reveals that ~90% of the cells arrive at the glomerular layer after day post injection (DPI) 7.

39 gic granule cells (GCs) and cells within the glomerular layer, although evidence supporting lateral i

40 el of the OB neuronal network including both glomerular layer and external plexiform layer (EPL) comp

41 of olfactory bulb inhibitory neurons in the glomerular layer and granule cell layer that innervate m

42 These oscillations arise in the glomerular layer and may be generated, in part, by the i

43 ion and later hypo-neuronal activity in both glomerular layer and mitral cell layer after TBI, which

44 ese output neurons, located primarily in the glomerular layer and superficial internal cell layer, ha

45 mpanied by the regrowth of axons into the OB glomerular layer and the return of smell perception.

46 Po2 has similar values in the olfactory bulb glomerular layer and the somatosensory cortex, whereas t

47 vity was heavy in the external plexiform and glomerular layers and localized to periglomerular somata

48 atterns (SAPs) in the olfactory nerve layer, glomerular layer, and external plexiform layer.

49 of calbindin-immunoreactive profiles in the glomerular layer, and parvalbumin-immunoreactive profile

50 atures appear to be encoded spatially in the glomerular layer, and the identity of the odorant may be

51 m layer, moderate in the olfactory nerve and glomerular layers, and localized to granule cells, mitra

52 d that distinct, functional odor maps in the glomerular layer are established from birth.

53 neural activation across the olfactory bulb glomerular layer are not stable in this respect; rather,

54 l glia the apical process does not enter the glomerular layer but instead ramifies within the externa

55 synapses; synaptic density is reduced in the glomerular layer but not the external plexiform layer, l

56 in specific layers in the OB, including the glomerular layer but not the granule cell layer.

57 optical responses in the olfactory nerve and glomerular layers but only small responses within the ex

58 ulb, BACE was expressed predominantly in the glomerular layer, but labeling intensity within individu

59 Noradrenergic terminals are found in the glomerular layer, but noradrenaline receptors do not see

60 fore, blocking inhibition originating in the glomerular layer, but not granule-cell-mediated inhibiti

61 ed the response of the entire olfactory bulb glomerular layer by using a high-resolution [14C]-2-deox

62 Neural activity was mapped across the entire glomerular layer by using the inverted question mark(14)

63 the superficial granule cells deep to those glomerular layer cells.

64 150 ms after stimulation and are mediated by glomerular layer circuits.

65 into glomerular knots within the presumptive glomerular layer, dendrites of individual mitral cells i

66 ds showing that odors elicit activity within glomerular layer domains in the mammalian OB, and extend

67 olution functional MRI at 7 T, combined with glomerular-layer flat maps, to reveal responses to aliph

68 (ErbB4(+)) neurons are mainly located in the glomerular layer (GL) and granule cell layer (GCL) and d

69 ed (M/T) cell dendrites were observed in the glomerular layer (GL) and juxtaglomerular external plexi

70 onto granule cells or bath application after glomerular layer (GL) excision failed to increase mIPSCs

71 DAergic interneurons are located in the glomerular layer (GL) where they participate in the proc

72 of serotonergic fibers, particularly in the glomerular layer (GL), where they are thought to gate in

73 erficial external plexiform layer (sEPL) and glomerular layer (GL).

74 amplitudes of which were largest within the glomerular layer (GL); smaller amplitude responses were

75 ulb (OB), alpha7 expression localizes in the glomerular layer; however, the functional role of alpha7

76 , and the projection onto the bulb fills the glomerular layer in its entirety.

77 ites and by activating sensory inputs in the glomerular layer in truncated GCs lacking dendrodendriti

78 n of interneurons located in the granule and glomerular layers in the olfactory bulb.

79 tribution of activated neurons in the mature glomerular layer, in which the boundaries of individual

80 minalis ganglion innervating the mitral cell/glomerular layer (MC/GL).

81 s, are due to weaker excitation and stronger glomerular-layer-mediated inhibition.

82 and TCs emerge in part due to differences in glomerular-layer-mediated inhibition.SIGNIFICANCE STATEM

83 within the bulb, with one set located in the glomerular layer mediating suppression of MC spiking acr

84 Immunoreactivity to GluR1 was heavy in the glomerular layer, moderate in the external plexiform lay

85 the demand for olfactory interneurons in the glomerular layer modulates cell turnover in the RMS, but

86 of the GABAergic/dopaminergic subtype in the glomerular layer, no information exists concerning the g

87 eonates, focal postsynaptic responses in the glomerular layer occurred in the form of clusters of act

88 In the glomerular layer of adults, many juxtaglomerular neurons

89 of apoE mRNA were found in astrocytes in the glomerular layer of olfactory bulbs and in Bergmann glia

90 was intense immunofluorescence signal in the glomerular layer of the accessory olfactory bulb and in

91 on of glutamatergic neurons (VGLUT3+) in the glomerular layer of the adult mouse OB as well as severa

92 Fos-B, but not Jun-D, CREB, or pCREB, in the glomerular layer of the ipsilateral olfactory bulb.

93 ake of [14C]2-deoxyglucose (2-DG) within the glomerular layer of the main olfactory bulb and that the

94 to systematically different odorants in the glomerular layer of the main olfactory bulb of rats.

95 However, as the axons approach the glomerular layer of the OB, axons from OSNs expressing t

96 l cavity project to localized regions in the glomerular layer of the OB.

97 the CA1 region of the hippocampus (top) and glomerular layer of the olfactory bulb (bottom) of anaes

98 erence is reflected in the separation of the glomerular layer of the olfactory bulb (OB) into dorsome

99 The glomerular layer of the olfactory bulb (OB) receives hea

100 r filtering out weak olfactory inputs in the glomerular layer of the olfactory bulb via the activatio

101 Neural activity across the entire glomerular layer of the olfactory bulb was mapped quanti

102 of odorants are represented spatially in the glomerular layer of the olfactory bulb, we used metaboli

103 ation of intrinsic signal responses from the glomerular layer of the olfactory bulb.

104 dient: lowest in the SVZa and highest in the glomerular layer of the olfactory bulb.

105 thelium and in the olfactory nerve layer and glomerular layer of the olfactory bulb.

106 gic trigeminal sensory fibers also enter the glomerular layer of the olfactory bulb.

107 terns of [(14)C]2-deoxyglucose uptake in the glomerular layer of the olfactory bulb.

108 terns of 2-deoxyglucose (2-DG) uptake in the glomerular layer of the rat olfactory bulb also were see

109 spatial activity patterns across the entire glomerular layer of the rat olfactory bulb evoked by oxy

110 of evoked neural activity across the entire glomerular layer of the rat olfactory bulb using primari

111 with unique spatial response patterns in the glomerular layer of the rat olfactory bulb.

112 Er81-positive cells in the granule cell and glomerular layers of the olfactory bulb derive from the

113 heir final positions in the granule cell and glomerular layers of the olfactory bulb in the same prop

114 tream (RMS) to populate the granule cell and glomerular layers of the olfactory bulb.

115 We injected neural tracers into the glomerular layer on one side of the bulb and examined th

116 classes of GABAergic neurons of the mouse OB glomerular layer, periglomerular (PG) and short axon (SA

117 e, we identify the first selective marker of glomerular layer-projecting deep short-axon cells (GL-dS

118 synaptic nicotinic and GABAergic currents in glomerular layer-projecting interneurons.

119 s entirely dependent on circuitry within the glomerular layer, rather than GCs, and it involved GABAe

120 tage-sensitive dye signals recorded from the glomerular layer reflect activity in periglomerular cell

121 Individual regions of the glomerular layer responded specifically to isoamyl ester

122 The optically recorded glomerular layer response was largely resistant to bath

123 unt of deoxyglucose uptake and extent of the glomerular layer showing high activity.

124 foci and were distributed widely across the glomerular layer, showing low overlap between trained an

125 Within the glomerular layer, the production of tyrosine hydroxylase

126 L-dSAC axons arborize extensively across the glomerular layer to provide highly divergent yet selecti

127 within the olfactory bulb extending from the glomerular layer to the granule cell layer that can be v

128 The glomerular layer was hypocellular, because of a decrease

129 Activity throughout the entire glomerular layer was measured as uptake of [(14)C]2-deox

130 nally, whereas the mechanosensitivity in the glomerular layer was observed repeatedly in the beta-glo

131 owed that homing of NPCs specifically to the glomerular layer was reduced in MT1-MMP-deficient mice i

132 anges in 2-DG uptake occur across the entire glomerular layer, we have mapped uptake throughout the l

133 atial patterns of neuronal activation in the glomerular layer were evident from birth, were sharply d

134 Large areas of the glomerular layer were not labeled by either lectin.

135 ween overlapping afferent streams within the glomerular layer were observed and partially characteriz

136 rough the olfactory nerve layer and into the glomerular layer, where its amplitude rapidly declined.

137 stricted to the periglomerular region of the glomerular layer, whereas c-met was expressed in the MCL

138 al TCs (eTCs), which are a TC subtype in the glomerular layer with large, direct OSN signals and capa