ライフサイエンスコーパス: chemoreception

1 2 to regulate breathing (central respiratory chemoreception).

2 n of ASICs in the VLM contributes to central chemoreception.

3 oth sexes, suggesting their putative role in chemoreception.

4 ting towards an 'optimization' for efficient chemoreception.

5 nergic signalling is a unique feature of RTN chemoreception.

6 previously identified neuromodulators of RTN chemoreception.

7 planation of their importance to respiratory chemoreception.

8 , including genes regulating ion balance and chemoreception.

9 phobic olfactory cues by a "tactile" form of chemoreception.

10 retrotrapezoid nucleus (RTN) contributes to chemoreception.

11 ortance of medullary 5-HT neurons in central chemoreception.

12 etween the two competing theories of central chemoreception.

13 P2 receptor signaling in central respiratory chemoreception.

14 ctions are consistent with a role in central chemoreception.

15 a, thus playing an important role in central chemoreception.

16 K1R-ir neurons and processes are involved in chemoreception.

17 es" has added further interest in intranasal chemoreception.

18 al respiratory group, is involved in central chemoreception.

19 ntage of neurons not involved in respiratory chemoreception.

20 hemenon which is not directly linked with O2 chemoreception.

21 s currently proposed for the mechanism of CB chemoreception.

22 ness, (2) participate in central respiratory chemoreception, (3) stimulate breathing frequency, and (

23 he RTN and serotonergic cells to respiratory chemoreception also relies on many other types of eviden

24 gic (5-HT) neurons are implicated in central chemoreception and 5-HT abnormalities are present in man

25 nce factors or sensory enzymes involved with chemoreception and c-di-GMP signalling.

26 breathing that are important in central CO2-chemoreception and for gating active expiration.

27 nt receptors) and pseudogene accumulation in chemoreception and P450 genes compared with A. mellifera

28 The involvement of amphidial secretions in chemoreception and the behavioral and electrophysiologic

29 region (MRR) have been implicated in central chemoreception and the modulation of the ventilatory res

30 3- buffer is essential for the expression of chemoreception and to distinguish between pHi and pHo in

31 nteract with the surrounding environment via chemoreception, and in social insects such as ants, chem

32 l tentacles serve contact- or short-distance chemoreception, and SSCs and the rhinophores function fo

33 For chemoreception, animals are believed to orient by compar

34 1R)-expressing neurones that are involved in chemoreception at the retrotrapezoid nucleus are also pr

35 ) may serve as molecular sensors for central chemoreception because they are highly expressed in mult

36 e the extent to which ATP contributes to RTN chemoreception both in vivo and in vitro, and whether pu

37 h were previously established in respiratory chemoreception, but do not innervate respiratory motor n

38 ignalling in respiratory control and central chemoreception by characterising the profile of the P2X

39 (the P box) in the periplasmic domain alter chemoreception by Nart and signaling by NarX similarly.

40 o which purinergic signalling contributes to chemoreception by RTN neurons is not clear and the mecha

41 spel the theory that ACh is required for RTN chemoreception by showing that ACh, similar to serotonin

42 th types, we evaluated their role in central chemoreception by specific cell killing.

43 in the integration of peripheral and central chemoreception (carotid bodies, chemoreceptor afferents,

44 l known about the sense of taste, or contact chemoreception, compared with other sensory modalities,

45 itivity, the notion that central respiratory chemoreception could rely on a few specialized neurons s

46 s of positive selection in genes involved in chemoreception, detoxification and digestion, and copy n

47 contribution of purinergic signalling to RTN chemoreception did not increase with temperature (22-35C

48 can be modified by a prior period of altered chemoreception during exercise.

49 li and/or cAMP may play an important role in chemoreception, especially in titrating the release of t

50 wn, we now show that comparable progesterone chemoreception exists in the invertebrate monogonont rot

51 luding tandem expansions of genes related to chemoreception, feeding, and digestion that possibly con

52 ception, and in social insects such as ants, chemoreception functions to mediate diverse behaviors in

53 CO(2), probably do not contribute to central chemoreception, given that they innervate sympathetic ef

54 s in pH to regulate breathing (i.e., central chemoreception) have remained incompletely understood, i

55 mbrane channel hypothesis of carotid body O2 chemoreception, hypoxia suppresses K+ currents leading t

56 n system participates importantly in central chemoreception in a vigilance-state- and diurnal-cycle-d

57 omeostasis in renal epithelial cells and CO2 chemoreception in brainstem neurons.

58 Most studies on chemoreception in decapods have focused on the prominent

59 iration, photosynthesis in algae and plants, chemoreception in insects, and even global warming .

60 We consider recent progress in understanding chemoreception in the fly, including the identification

61 channels in postnatal maturation of hypoxic chemoreception in the rat carotid body.

62 did not support the redox hypothesis of O(2) chemoreception in the whole carotid body.

63 is known about the cells or mechanisms of O2 chemoreception in vertebrates other than mammals.

64 in the medulla are both involved in central chemoreception in vivo.

65 to define the cellular mechanisms of central chemoreception in vivo.

66 re thought to function as important sites of chemoreception including the nucleus of the solitary tra

67 In the RTN, mechanisms of chemoreception involve direct H(+)-mediated activation o

68 Chemoreception is essential for survival.

69 One of the early events in O2 chemoreception is inhibition of O2-sensitive K+ (KO2) ch

70 Insect chemoreception is mediated by a large and diverse superf

71 is that K+-O2 current is linked to events in chemoreception is not substantiated.

72 Central chemoreception is the mechanism by which CO(2)/H(+) -sen

73 Central chemoreception is the mechanism by which the brain regul

74 Central respiratory chemoreception is the mechanism by which the CNS maintai

75 A central question in insect chemoreception is whether signaling occurs via G-protein

76 Their contribution to central respiratory chemoreception may be behavior dependent or vary accordi

77 CO2 chemoreception may be mediated by the modulation of cert

78 Chemoreception, mediated by the odorant receptors on the

79 Females either rely less on 5-HT neurons in chemoreception or adapt more readily to the loss of 5-HT

80 d the rhinophores function for long-distance chemoreception or olfaction.

81 Chemoreception plays a crucial role in increasing mate e

82 understanding about the mechanisms of taste chemoreception, protein stabilization, etc.

83 Central respiratory chemoreception refers to the component of this homeostat

84 Central chemoreception refers to the detection within the brain

85 s underlying the purinergic component of RTN chemoreception remains unknown.

86 Nevertheless, the field of oxygen chemoreception still presents the general observer with

87 itability or specifically related to central chemoreception, such as potassium channels.

88 antic confusion between chemosensitivity and chemoreception (the mechanism by which CO(2) or pH activ

89 A long-standing theory posits that central chemoreception, the CNS mechanism for CO(2) detection an

90 Central chemoreception, the highly sensitive ventilatory respons

91 ins neurons thought to contribute to central chemoreception, the process by which systemic hypercapni

92 n neurotransmitters such as ACh modulate RTN chemoreception, the results of the present study provide

93 he assumptions that underlie the distributed chemoreception theory to a critical analysis.

94 The 'distributed chemoreception theory' attributes the central chemorefle

95 ences identified include a bias in bumblebee chemoreception towards gustation from olfaction, and str

96 host adaptation, including gene families for chemoreception, toxin and insecticide metabolism, cuticl

97 instead, cilia elongated and cilia-mediated chemoreception was abnormal.

98 ment of the control of breathing and central chemoreception, which may be pertinent to SIDS.