ライフサイエンスコーパス: main olfactory bulb

1 sters of glomeruli situated ventrally in the main olfactory bulb.

2 tors (CB1Rs) are present in glomeruli of the main olfactory bulb.

3 e newly described vasopressin neurons in the main olfactory bulb.

4 g fluorescence in tissue slices of the mouse main olfactory bulb.

5 e glomerular layer, across wide areas of the main olfactory bulb.

6 t response properties, and projection to the main olfactory bulb.

7 ential and reproducible projections onto the main olfactory bulb.

8 of the predominant alpha CaMKII in the mouse main olfactory bulb.

9 rons penetrate into the deeper layers of the main olfactory bulb.

10 trol of olfaction, with the exception of the main olfactory bulb.

11 helium and in virtually all glomeruli in the main olfactory bulb.

12 rcle, the anterior olfactory nucleus and the main olfactory bulb.

13 rated in the internal plexiform layer of the main olfactory bulb.

14 In the main olfactory bulb, activation of group I metabotropic

15 pressed in the olfactory sensory epithelium, main olfactory bulb and accessory olfactory bulb.

16 distribution of UEA vs. DBA labeling in the main olfactory bulb and are consistent with the hypothes

17 proteins are highly concentrated in the rat main olfactory bulb and are localized in distinct neuron

18 ive parallel olfactory circuits, four in the main olfactory bulb and one in the accessory olfactory b

19 projections innervate multiple layers of the main olfactory bulb and strongly influence odor discrimi

20 se (2-DG) within the glomerular layer of the main olfactory bulb and that the amount of 2-DG accumula

21 he glomerular and granule cell layers of the main olfactory bulb and the striatum.

22 information and acts as a relay between the main olfactory bulbs and higher brain regions such as th

23 licit responses in the olfactory epithelium, main olfactory bulb, and olfactory (piriform) cortex of

24 chemosensory information, the accessory and main olfactory bulb (AOB and MOB, respectively).

25 xons to glomeruli in the ventral area of the main olfactory bulb are involved in processing of inform

26 cillatory activity in the deep layers of the main olfactory bulb, as well as dendrodendritic synaptic

27 siological properties of mitral cells in rat main olfactory bulb brain slice preparations.

28 gic neurons innervate multiple layers in the main olfactory bulb but the precise circuitry of this in

29 Similarly, axons innervating the main olfactory bulb, but not the accessory olfactory bul

30 onomolecular odorants are represented in the main olfactory bulb by distinct spatial patterns of acti

31 Axons in all four main olfactory bulb circuits exhibited axonal localizati

32 In rodents, each main olfactory bulb contains two mirror-symmetric glomer

33 Glomeruli at the posterior margin of the main olfactory bulb differ in several respects from thos

34 of Y1 immunoreactivity were found the in the main olfactory bulb, dorsomedial part of suprachiasmatic

35 lasses of principal neurons in the mammalian main olfactory bulb, exhibit morphological differences b

36 Granule and periglomerular cells in the main olfactory bulb express group I metabotropic glutama

37 aracterize neuronal populations in the mouse main olfactory bulb, focusing on glomerular populations.

38 Axonal projections from these neurons to the main olfactory bulbs form reproducible patterns of glome

39 excitatory mitral projection neurons of the main olfactory bulb; here, these two classes of neurons

40 munofluorescence in glomeruli throughout the main olfactory bulb indicated a heterogeneous distributi

41 observed in olfactory structures such as the main olfactory bulb (internal granular layer), anterior

42 erns and neuronal olfactory responses in the main olfactory bulb, intracellular recordings were combi

43 fortunately, the mechanism and extent of the main olfactory bulb (MOB) and accessory olfactory bulb (

44 nt receptors and segregated glomeruli in the main olfactory bulb (MOB) are assembled into integrated

45 Granule cells (GCs) in the main olfactory bulb (MOB) are presumed to sculpt activit

46 In cerebellar stellate, thalamic relay, and main olfactory bulb (MOB) deep short-axon cells of Wista

47 eceptor neurons (ORNs) project to the rodent main olfactory bulb (MOB) from spatially distinct air ch

48 from the accessory olfactory bulb (AOB) and main olfactory bulb (MOB) in acute mouse brain slices to

49 The main olfactory bulb (MOB) is richly targeted by LC fiber

50 blished that a subset of mitral cells in the main olfactory bulb (MOB) projects directly to the media

51 The main olfactory bulb (MOB) receives a dense projection fr

52 born cells in the dentate gyrus (DG) and the main olfactory bulb (MOB) was determined in sheep.

53 ted myelin break down in the neuropil of the main olfactory bulb (MOB), cerebral cortex (CTX), caudat

54 In the main olfactory bulb (MOB), inhibitory circuits regulate

55 In the main olfactory bulb (MOB), odorants are ultimately repre

56 In the main olfactory bulb (MOB), the first station of sensory

57 culline/D,L-homocysteic acid mixture) of the main olfactory bulb (MOB).

58 small fraction of mitral cells in the mouse main olfactory bulb (MOB).

59 y defasciculated and a subset innervates the main olfactory bulb (MOB).

60 ion of a distinct subset of glomeruli in the main olfactory bulb (MOB).

61 ing their axons to their terminations in the main olfactory bulb (MOB).

62 m (MOE) send their axons to glomeruli in the main olfactory bulb (MOB); and (2) an accessory olfactor

63 We tested whether the main olfactory bulb (OB) of mice mediates daily changes

64 eling data suggest that the circuitry of the main olfactory bulb (OB) plays a critical role in olfact

65 the number of GABAergic interneurons in the main olfactory bulb (OB).

66 od to image bioluminescence in vivo from the main olfactory bulbs (OB) of intact and SCN-lesioned (SC

67 f mitral cells was recorded in vivo from the main olfactory bulb of freely breathing anesthetized rat

68 rent odorants in the glomerular layer of the main olfactory bulb of rats.

69 ons (primary neurons), to the posteroventral main olfactory bulb (PV MOB) in mice.

70 g circuitry of this cholinergic input to the main olfactory bulb remains unclear, however.

71 Electrophysiological studies in rat main olfactory bulb slices demonstrated that the mGluR a

72 minalis, most divisions of the amygdala, the main olfactory bulb, the endopiriform nucleus, the claus

73 n the basal forebrain project heavily to the main olfactory bulb, the first processing station in the

74 In the main olfactory bulb, the largest differences in laminar

75 In addition to receiving afferents from the main olfactory bulb, the olfactory amygdala receives aff

76 Mitral/tufted (M/T) cells of the main olfactory bulb transmit odorant information to high

77 By 42 days of age, main olfactory bulb volume was significantly decreased i

78 t study, the distribution of IP3R in the rat main olfactory bulb was determined by immunohistochemist

79 such complex mixtures are represented in the main olfactory bulb, we analysed the electrophysiologica

80 onal synchronization occurs in the mammalian main olfactory bulb where mitral cells that project to t

81 heavily labeled for leu-enkephalin, and the main olfactory bulb, where only met-enkephalin was obser

82 ombinatorial fashion across glomeruli in the main olfactory bulb, with each glomerulus corresponding