ライフサイエンスコーパス: olfactory organ

1 r chemosensory specialization (proteomics of olfactory organs).

2 or classes expressed in the single zebrafish olfactory organ.

3 ed predominantly in antenna, mosquito's main olfactory organ.

4 of olfactory receptor neurons throughout the olfactory organ.

5 odor coding by the receptor repertoire of an olfactory organ.

6 sociated with the aesthetasc sensilla in the olfactory organ.

7 th known and novel properties of the lobster olfactory organ.

8 esented by these clones were enriched in the olfactory organ.

9 hin the olfactory placode to form the mature olfactory organ.

10 regions, and without removing the peripheral olfactory organ.

11 ity to characterize all neurons in an entire olfactory organ.

12 any structurally distinct transcripts in the olfactory organs.

13 maxillary palp, the simpler of the fly's two olfactory organs.

14 sophila maxillary palp, one of the two adult olfactory organs.

15 thesis in the jaw region, pectoral fins, and olfactory organs.

16 nterpreted by sampling air pumped over their olfactory organs.

17 mbrane domain proteins that are expressed in olfactory organs.

18 reliable practical sensor device that mimics olfactory organs.

19 Unilateral olfactory organ ablations were performed on anesthetized

20 While IRs are expressed in olfactory organs across Protostomia, ORs have been hypot

21 s to placode-derived features, including the olfactory organ, adenohypophysis, lens, inner ear, later

22 any terrestrial vertebrates comprises a main olfactory organ and a vomeronasal organ each containing

23 that morphologically resemble the vertebrate olfactory organ and adenohypophysis.

24 ty against CR and CB was investigated in the olfactory organ and brain of Polypterus senegalus and co

25 y binds to the non-sensory epithelium of the olfactory organ and causes severe olfactory histopatholo

26 ephalon, and spinal cord) and the developing olfactory organ and retina.

27 Cells giving rise to progeny in both the olfactory organ and telencephalon express the distal-les

28 orylating G-protein-coupled receptors in the olfactory organ and the brain, respectively.

29 ngs support the hypothesis that the separate olfactory organ and VNO of terrestrial vertebrates arose

30 in the liver, and sult2st3 was found in the olfactory organs and choroid plexus.

31 , which display substantial asymmetry of the olfactory organs and forebrain.

32 hologies of the various sensory cells in the olfactory organs and skin were examined using antibodies

33 Expression of Scrib is widespread in olfactory organs and the central nervous system.

34 e functional roles in tissues other than the olfactory organ, and further, suggest that these functio

35 melanogaster is equipped with two peripheral olfactory organs, antenna and maxillary palp.

36 ve ORs in the transcriptomes of the two main olfactory organs, antenna and palp, of the locust Schist

37 Both gut and olfactory organs are the primary sites of invasion.

38 lescens) are expressed in the embryonic eye, olfactory organ, brain, and arms.

39 pressed in the respective nerve cords, eyes, olfactory organs, brain, and limbs.

40 It was most abundant in the brain and the olfactory organ but was absent in the eye/eyestalk.

41 of phospholipase C was isolated from lobster olfactory organ cDNA libraries and named lobPLCbeta.

42 coiled-coil protein and is expressed in the olfactory organs, central nervous system, and male repro

43 A. gambiae that are selectively expressed in olfactory organs, contain approximately seven transmembr

44 fan that serves as a presumptive tactile and olfactory organ during copulation.

45 ion of the anatomical changes of the Xenopus olfactory organ during metamorphosis.

46 ructural and cellular changes of the Xenopus olfactory organ during metamorphosis.

47 Simultaneous recordings in vivo from the olfactory organ [electro-olfactogram (EOG) or integrated

48 ndividual receptor neurons in the peripheral olfactory organ extend long axons into the olfactory bul

49 early marker of neural differentiation, the olfactory organs first differentiate at about stage 16 w

50 Analysis of serial sections from entire olfactory organs for epithelial area and patterns of imm

51 Removal of the olfactory organ in adult zebrafish results in a signific

52 truct a receptor-to-neuron map for an entire olfactory organ in Drosophila and find that two receptor

53 nary implications of the loss of a dedicated olfactory organ in spiders and its effects on the mushro

54 tly visualized in living mosquitoes from all olfactory organs, including the antenna.

55 Single cell RNA-Seq of the adult zebrafish olfactory organ indicated widespread loss of olfactory r

56 rise to the paired peripheral sense organs (olfactory organs, inner ears and anamniote lateral line

57 The trout olfactory organ is colonized by abundant symbiotic bacte

58 analysis of all neuronal types in this model olfactory organ is discussed in terms of its functional

59 This fish provides a model in which the olfactory organ is easily accessible for removal, the an

60 In conclusion, the olfactory organ is important in the preservation of norm

61 ansition zone resembled neither VNO nor main olfactory organ (MO) receptor cells and may represent th

62 etrical neurons was found in the peripheral "olfactory organ." NADPH-d-reactive non-neuronal cells we

63 extended previous descriptions of HA in the olfactory organ, nerve, and lobe, and describe HDC stain

64 on of odor receptor (Or) genes in the proper olfactory organ of Drosophila, and we identify an elemen

65 sed in the third antennal segment, the major olfactory organ of Drosophila.

66 of myeloid and lymphoid cells located in the olfactory organ of fish.

67 The olfactory organ of goldfish appears as a rosette, with t

68 highly expressed in the adult antennae, the olfactory organ of insects.

69 no differential gene expression in gustatory/olfactory organs of adult females with different oviposi

70 Olfactory organs of adult zebrafish were permanently and

71 an odorant binding protein expressed in the olfactory organs of Drosophila melanogaster that is requ

72 Studies of the two major olfactory organs of rodents, the olfactory mucosa (OM) a

73 The influence of the olfactory organ on maintenance of olfactory bulb structu

74 very rapid proinflammatory responses in the olfactory organ (OO), but dampened inflammation in the o

75 o cause neuroimmune responses in the teleost olfactory organ (OO).

76 edominantly to a 9 kb transcript in RNA from olfactory organ, pereiopod, brain, and eye-eyestalk and

77 130 kDa band in olfactory aesthetasc hairs, olfactory organ, pereiopod, dactyl, and brain.

78 Analysis of bulbs following olfactory organ removal revealed a significant loss of i

79 and associated sensory organs including the olfactory organ, retina, lens, cornea, otic vesicle, lat

80 ly from widely separated lamellae within the olfactory organ suggest that PWs are initiated in the se

81 d expression of biotransformation enzymes in olfactory organs suggests that they play an important ro

82 ripts that were more abundant in the lobster olfactory organ than in brain, eye/eyestalk, dactyl, per

83 We have examined odor coding in a model olfactory organ, the maxillary palp of Drosophila.

84 ressed specifically or preferentially in the olfactory organs, the antennae.

85 ead expression of the dsc1 gene in the major olfactory organs, the third antennal segment and the max

86 imals revealed that most, if not all, of the olfactory organ was missing on the ablated side, and the

87 scribed for squid OE, paraformaldehyde-fixed olfactory organs were cryosectioned (10 microm), double-

88 tion of rhythmically active neurons in their olfactory organs with the potential to peripherally enco

89 eptor families are segregated into different olfactory organs, with type 2 vomeronasal receptor (v2r)