ライフサイエンスコーパス: chemical stimulation

1 myocytes and fibroblasts induced by physico-chemical stimulation.

2 ies of these nanoassemblies in response to a chemical stimulation.

3 s elegans animals under precise microfluidic chemical stimulation.

4 cell death in response to virus infection or chemical stimulation.

5 ternally applied mechanical, electrical, and chemical stimulation.

6 cal stimulation and all responded to noxious chemical stimulation.

7 ked in experimental animals by electrical or chemical stimulation.

8 docrine cells respond to both mechanical and chemical stimulation.

9 cted from simple occlusion between light and chemical stimulation.

10 mical receptors responsive to mechanical and chemical stimulation.

11 d for sensitivity to mechanical, thermal and chemical stimulation.

12 somatic afferents to mechanical, thermal and chemical stimulation.

13 adjacent to individual mast cells following chemical stimulation.

14 Also striking was the finding that chemical stimulation (50 mm Glu) of the vBNST yielded lo

15 Conversely, the response to chemical stimulation alone (based on physiological CO2/H

16 ic multifunctional device that is capable of chemical stimulation and electrical sensing at the same

17 ry effects on dorsal horn neurones evoked by chemical stimulation at identified pressor and depressor

18 This chemical stimulation caused consistent excitatory cardio

19 m were necessary for tears evoked by noxious chemical stimulation (CO2 pulses) or drying of the ocula

20 brain region, such as lesion, electrical and chemical stimulation, electrophysiology and in vivo micr

21 plate, tail flick) and to persistent noxious chemical stimulation (formalin) and (2) the antinocicept

22 matrix and when presented with a controlled chemical stimulation from the artificial vasculature, th

23 tivation of LC neurons through electrical or chemical stimulation has also led to important insights,

24 Class 2 neurones were strongly inhibited by chemical stimulation in either sector of the PAG.

25 s throughout the spinal dorsal horn, noxious chemical stimulation in the normal rat only induces inte

26 ation is consistent with a potential role of chemical stimulation in triggering dyspeptic symptoms.

27 ding facilitation produced by electrical- or chemical-stimulation in the NGC and NGCalpha also signif

28 Electrical or chemical stimulation increased AbetaO synaptic localizat

29 We observed that repeated chemical stimulation led to a reversible reduction in th

30 esponding to mechanical, noxious thermal and chemical stimulation; mechanothermal nociceptors respond

31 In addition, electrical and chemical stimulation of A7 neurons produces antinocicept

32 Chemical stimulation of cAMP production by Mtb within ma

33 icrom) and deeper thoracic spinal neurons to chemical stimulation of cardiac afferents and effects of

34 Results showed that chemical stimulation of cardiac afferents excited superf

35 , both spontaneous activity and responses to chemical stimulation of cardiac afferents significantly

36 This study examined whether site-directed chemical stimulation of DMH/PeF neurons evoked changes i

37 Chemical stimulation of DMH/PeF neurons evoked significa

38 Chemical stimulation of DMH/PeF neurons evokes substanti

39 The demonstration of localized chemical stimulation of excitable cells illustrates the

40 ve examined the influences of electrical and chemical stimulation of Gi and DPGi inhibitory sites on

41 bition of glycolysis decreased SSC activity, chemical stimulation of glycolysis or transfection of ac

42 hypoxia-inducible factor (HIF-1alpha) after chemical stimulation of human pancreatic tumor cells enc

43 iation of central sensitization triggered by chemical stimulation of meningeal nociceptors.

44 Focal electrical or chemical stimulation of MPO in anesthetized rats induced

45 asured cardiovascular responses to localized chemical stimulation of neurons in area infraradiata of

46 Chemical stimulation of nonischemic ipsilateral cortex b

47 been considered to result from mechanical or chemical stimulation of pain-sensitive structures of the

48 characterize cardiovascular responses to the chemical stimulation of sites located in the medullary l

49 t to caudal regions of the PBN responsive to chemical stimulation of the anterior tongue as well as m

50 In the middle LPBN chemical stimulation of the dorsal PAG selectively incre

51 Tachycardia evoked by chemical stimulation of the dorsomedial hypothalamus can

52 displayed increased nociceptive responses to chemical stimulation of the face and hyperalgesic respon

53 The mechanism of cardiovascular responses to chemical stimulation of the hypothalamic arcuate nucleus

54 Chemical stimulation of the insula using L-glutamate was

55 ransiently abolishes behavioral responses to chemical stimulation of the intestine.

56 Chemical stimulation of the lateral or ventrolateral col

57 Chemical stimulation of the lateral PAG produces hyperte

58 acterized the effects of both electrical and chemical stimulation of the LH on 36 DMNV and 14 NST neu

59 We now report that chemical stimulation of the MeA enhanced levels of extra

60 Chemical stimulation of the MPO excited 17/97 cells and

61 responses to electrical, mechanical, and to chemical stimulation of the muscle.

62 r the increase in sympathetic tone caused by chemical stimulation of the nasal passages with ammonia

63 Chemical stimulation of the PVN by unilateral microinjec

64 ervated rats: 1) tachycardia elicited by the chemical stimulation of the PVN was mediated via both in

65 halamic activity on Up states, electrical or chemical stimulation of the thalamus triggered cortical

66 -, or Q-best on the basis of its response to chemical stimulation of the tongue.

67 However, stronger chemical stimulation of the vBNST (100 mm Glu) completel

68 tivation of DA neuron firing, the effects of chemical stimulation of the vSub on ventral tegmental ar

69 Chemical stimulation of their dural receptive fields wit

70 , cAMP, or MAPK pathway activation by either chemical stimulation or cotransfection of active cascade

71 threat and is also elicited by electrical or chemical stimulation over the rostro-caudal extent of th

72 , for the first time, that nerve impulses or chemical stimulation promote Ca2+ entry into PSNTs, incl

73 Neuronal responses to electrical and chemical stimulation showed specific firing patterns of

74 Yet, no subretinal electrical or chemical stimulation study has stimulated the OFF and ON

75 afferent sensitivity to both mechanical and chemical stimulations, suggesting that somatostatin play

76 Direct mechanical and chemical stimulation to peripheral nociceptors, peripher

77 mplants capable of delivering electrical and chemical stimulation to targeted regions of the central

78 energy levels for mechanical stimulation and chemical stimulation were comparable.

79 t, chorda tympani nerve responses to lingual chemical stimulation were maintained at 10 d but were el

80 e responses of thermally-sensitive fibers to chemical stimulation were modest at best with an absence

81 The CBF effects evoked from DPAG and VPAG by chemical stimulation were preserved in spinalized rats s

82 nteract with cocultured cells by physical or chemical stimulation, which significantly mediate their

83 itization in dorsal horn neurons produced by chemical stimulation with capsaicin.

84 l stimulus (up to 265 +/- 42%, P = 0.022) or chemical stimulation with formyl-methylleucylphenylalani

85 menon have been limited to digital (or step) chemical stimulation with little control over the tempor

86 Furthermore, RSR was enhanced by chemical stimulation with potassium chloride.

87 PAG comparably elevated AP and CBF, whereas chemical stimulation with the D,L-homocysteine produced