ライフサイエンスコーパス: olfactory pathway

1 pathology in projection neurons (PNs) of the olfactory pathway.

2 sensory information at an early stage of the olfactory pathway.

3 oursegregation in downstream circuits of the olfactory pathway.

4 ted whether HHV-6 may infect the CNS via the olfactory pathway.

5 n to chemosensory coding along the accessory olfactory pathway.

6 ative metabolism at the first synapse on the olfactory pathway.

7 oliferate to form new neurons in the central olfactory pathway.

8 predict the existence of a yet-undiscovered olfactory pathway.

9 volved through odour images generated in the olfactory pathway.

10 o take advantage of this unique and critical olfactory pathway.

11 xtension of olfactory axons (OAs) within the olfactory pathway.

12 on all classes of glial cells in the primary olfactory pathway.

13 xon growth during the initial genesis of the olfactory pathway.

14 n neuronal differentiation in the developing olfactory pathway.

15 ptation at the first synaptic step along the olfactory pathway.

16 g of how odors are encoded by the peripheral olfactory pathway.

17 is not required for initial viral entry into olfactory pathway.

18 ct different functional contributions to the olfactory pathway.

19 for the normal development of the mammalian olfactory pathway.

20 ry bulb, the first processing station in the olfactory pathway.

21 he odor information by higher centers in the olfactory pathway.

22 ay contribute to the initial assembly of the olfactory pathway.

23 ral forebrain may constitute an extra-bulbar olfactory pathway.

24 d through activation of a single specialized olfactory pathway.

25 t (nonthalamic) and indirect (transthalamic) olfactory pathways.

26 y is restricted to projection neurons in the olfactory pathway; (4) neurogenesis in adult alpha-syn-T

27 it can be initiated even after disruption of olfactory pathways.(9) We investigated how subnucleus mu

28 Microarray screening of the injured olfactory pathway and of cultured OECs identified 102 ge

29 ls occupy discrete regions of the developing olfactory pathway and processes of gamma-aminobutyric ac

30 E virus initially enters the CNS through the olfactory pathways and initiates viral replication in th

31 many parallels in the functional anatomy of olfactory pathways and the organization of information-c

32 enin family member expression in the primary olfactory pathway, and because mechanisms of Wnt-Fz inte

33 f the oe during the early development of the olfactory pathway, and may influence differentiation and

34 istinct adhesive environments in the nascent olfactory pathway, and some of the molecules that charac

35 oad tuning and variability of neurons in the olfactory pathway,and by the distributed nature of olfac

36 zing in an identified glomerulus in the main olfactory pathway are morphologically and physiologicall

37 ese results support HHV-6 utilization of the olfactory pathway as a route of entry into the CNS.

38 punctate staining pattern in the developing olfactory pathway as early as E12.

39 In the olfactory pathway, as in the limbs, branchial arches, an

40 f pioneer neurons that prefigure the primary olfactory pathway before outgrowth of olfactory sensory

41 were expressed differentially in the primary olfactory pathway both during development and regenerati

42 ein, is extensively expressed in the primary olfactory pathway, but its function is unknown.

43 l of neurovirulence and neural spread in the olfactory pathway, but the Us9 deletion mutant of BHV-5

44 Exposures via the olfactory pathway can also lead to (anti-)inflammatory o

45 active for P0, including afferent visual and olfactory pathways, commissural and longitudinal tracts

46 em with unique neuronal architecture: a dual olfactory pathway comprising a medial projection-neuron

47 topographic maps in sensory systems, central olfactory pathways, corticocortical and commissural conn

48 The mammalian main olfactory pathway detects myriad volatile chemicals usin

49 The mammalian main olfactory pathway detects volatile chemicals using two f

50 genetic abnormalities includes disruption of olfactory pathway development.

51 alized Sema3A mRNA expression in the primary olfactory pathway during development, in adult rats, and

52 s between species in the organization of the olfactory pathway, from the nature of the odorant recept

53 ative importance of the MT and HB within the olfactory pathway have occurred during the evolution of

54 As in vertebrates, the olfactory pathway in Drosophila follows similar converge

55 ture and function of peripheral parts of the olfactory pathway in newly hatched and adult locusts.

56 ons, we investigated the organization of the olfactory pathway in queens, workers, and males of the e

57 adapted to guide the differentiation of the olfactory pathway in the developing forebrain.

58 ertaken both to examine the evolution of the olfactory pathway in the Eumalacostraca and to provide i

59 AL), the first synaptic relay of the central olfactory pathway in the insect brain.

60 Using calcium imaging, we identify olfactory pathways in D. sechellia that detect volatiles

61 e our understanding of the morphology of the olfactory pathways in H. americanus we also examined the

62 ment of vector control strategies, targeting olfactory pathways in larval-stage mosquitoes to reduce

63 has inspired theories about the role of the olfactory pathways in the development of cortical neurod

64 loss and the pathological involvement of the olfactory pathways in the formative stages of Alzheimer'

65 etween species across two well-characterized olfactory pathways, including regulatory genes controlli

66 fic channels in hardwired circuits along the olfactory pathway, insulated from influences of other od

67 d a conceptual framework that integrates the olfactory pathway into an understanding of the effects o

68 tion and neural processing in the peripheral olfactory pathway involve basic mechanisms that are univ

69 This loss of the entire primary olfactory pathway is accompanied by a failure of retinoi

70 nels at the earliest processing stage in the olfactory pathway leads to re-coding of odor identity to

71 the primary somatosensory cortex (S1) or the olfactory pathway of rats.

72 of two higher-order neuropils in the central olfactory pathway of the crayfish: the accessory lobe an

73 In the olfactory pathway of the moth Manduca sexta,we find that

74 Here, we explored pathologic changes in the olfactory pathway of transgenic (Tg) mice of both sexes

75 aturation, and synaptogenesis in the primary olfactory pathway of wild-type (WT) and apoE knockout (K

76 ronal populations has been documented in the olfactory pathways of both vertebrates and invertebrates

77 phenomenon through comparison of homologous olfactory pathways of Drosophila melanogaster and its cl

78 glomeruli, a feature that is not known from olfactory pathways of other animals.

79 the possible existence of homologies in the olfactory pathways of these eusocial Hymenoptera.

80 nal lobe, the first processing center of the olfactory pathway, of the moth Manduca sexta were studie

81 a degenerative spread of the disease through olfactory pathways, of neuroinflammatory events, or of t

82 initial sites of synaptic integration in the olfactory pathway, olfactory sensory axons terminate on

83 signaling is disrupted, distinct aspects of olfactory pathway patterning and differentiation are com

84 f information processing along the accessory olfactory pathway, projection neurons (mitral cells) dis

85 at parallel processing via the honeybee dual olfactory pathway provides enhanced odor processing capa

86 cts of sensory signaling along the accessory olfactory pathway remain largely unknown.

87 , we found that neuronal firing early in the olfactory pathway simultaneously conveyed fundamentally

88 suggesting a greater integration of the two olfactory pathways than traditionally believed.

89 ally separated into two subsystems: a 'main' olfactory pathway that detects and processes information

90 r results suggest that a novel Orco-mediated olfactory pathway that gains sensitivity to CO(2) in fli

91 t environmental odorants, and an 'accessory' olfactory pathway that is devoted to information about s

92 We focus on two integrative neuropils of the olfactory pathway, the antennal lobes and the mushroom b

93 During the initial assembly of the olfactory pathway, the behavior of olfactory axons chang

94 At the first stage of processing in the olfactory pathway, the patterns of glomerular activity e

95 eu)), there is a more discrete lesion to the olfactory pathway: The epithelium and bulb cannot be rec

96 is a noninvasive approach that utilizes the olfactory pathway to administer pharmacological agents d

97 tudies examine the inputs from each of these olfactory pathways to a population of neurons that plays

98 During embryogenesis, all neuropils of the olfactory pathway transiently expressed Sema 1a.

99 The impact of SARS-CoV-2 on the olfactory pathway was studied over several time points u

100 Cells of the olfactory pathway were found to express beta-galactosida

101 ces for early differentiation of the primary olfactory pathway-which comprises both craniofacial and

102 ed with tau accumulation in key areas of the olfactory pathway, with a particularly strong predictive

103 As in bees and ants, hornets display a dual olfactory pathway, with two major efferent tracts, the m