ライフサイエンスコーパス: olfactory pathway

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

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

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

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

5 volved through odour images generated in the olfactory pathway.

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

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

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

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

10 n neuronal differentiation in the developing olfactory pathway.

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

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

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

14 ct different functional contributions to the olfactory pathway.

15 oursegregation in downstream circuits of the olfactory pathway.

16 for the normal development of the mammalian olfactory pathway.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

41 genetic abnormalities includes disruption of olfactory pathway development.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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