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1 rates for the future investigation of aortic depressor afferent physiology, structural remodeling of
2 the pressor agent phenylephrine (PE) and the depressor agent sodium nitroprusside (SNP) in 57 urethan
4 t of VAGSTIM was specific for ERSNA, because depressor and bradycardia responses to VAGSTIM were unaf
5 tachycardic response which was followed by a depressor and bradycardic response; when high concentrat
6 l cerebrospinal (aCSF) fluid, confirmed that depressor and bradycardic responses are elicited from al
7 e medial subnucleus of the NTS (mNTS) elicit depressor and bradycardic responses via activation of io
9 njections of l-Glu remained unchanged, i.e., depressor and bradycardic responses were elicited from a
10 tory effects of E-2 in the mNTS resulting in depressor and bradycardic responses, on one hand, and in
15 (2) activation of these receptors results in depressor and bradycardic responses; (3) for a complete
16 In sham rats, BDNF evoked a dose-dependent depressor and sympatho-inhibitory effect and ANA-12 prod
18 EMG activity recorded from the frontalis and depressor anguli oris during a contrived expression.
19 during the horror look and the frontalis and depressor anguli oris during one of the contrived expres
20 cus major during smiling, the corrugator and depressor anguli oris during the sad look and the fronta
21 robably more prevalent in the corrugator and depressor anguli oris during the sad look, the frontalis
22 ocated in the caudal ventrolateral medullary depressor area (CVLM) in regulating/modulating cardiovas
23 ea (RVLM) and caudal ventrolateral medullary depressor area (CVLM), and the nucleus tractus solitariu
24 were found ipsilaterally in the pressor and depressor areas of the medulla and the spinal trigeminal
28 MS and control site responses to pressor and depressor challenges during sleep that resulted in somat
29 es differed in direction between pressor and depressor challenges, neural activity increased later in
31 phic color pattern in that levator (Lev) and depressor (Dep) of females tend to be much darker than t
32 We studied the Caenorhabditis elegans anal depressor development in larval males and hermaphrodites
34 ating that AT2 receptor does not exert acute depressor effects in these mice lacking AT1 receptors.
39 n that the M. protractor pterygoideus and M. depressor mandibulae act on the quadrate as a pure torqu
41 ntified leg motoneurons (such as the femoral depressor motoneuron) expressed detectable levels of TM-
42 th silence of the slow and fast trochanteral depressor motoneurons and activation of the common inhib
44 (fSR) makes direct cholinergic synapses with depressor motor neurons (MN) controlling that wing, incl
45 MGs and with differences in the responses of depressor motor neurons recorded in reduced, in vitro pr
47 levation/depression and trochanteral levator/depressor muscle bursts, suggesting that the neural modu
48 h simultaneously recorded differences in leg depressor muscle EMGs and with differences in the respon
50 lossal (GG) muscle is the main protruder and depressor muscle of the tongue and contributes to upper
53 y killing the SPC motor neurons and the anal depressor muscle: cells that directly contact the protra
55 ameter values are based on measurements from depressor muscles and observations of kinematics and dyn
56 s generated by slow contractions of hind leg depressor muscles and then stored by bending specialised
57 adhesive bandages (19 cases), wooden tongue depressors (n = 5), ostomy bags (n = 2), water circuitry
58 ited by electrical stimulation of the aortic depressor nerve (ADN) at 5 Hz or 15 Hz in urethane anest
60 of the solitary tract (NTS) receiving aortic depressor nerve (ADN) inputs was examined during blood p
61 ified according to their responses to aortic depressor nerve (ADN) stimulation: monosynaptic neurones
65 ormed during control, after bilateral aortic depressor nerve section, after bilateral cervical vagus
66 vagus nerve section, after bilateral aortic depressor nerve section, and during central aortic depre
71 ast three adult-specific muscles, the tergal depressor of the trochanter and dorsoventral muscles I a
72 n the number of fibers comprising the tergal depressor of the trochanter muscle (TDT, or jump muscle)
73 as TpnC41C is the main isoform in the tergal depressor of the trochanter muscle (TDT; jump muscle).
74 entobarbitone-anaesthetized animals, the jaw-depressor reflex (JDR) evoked by stimulation of the tong
78 Lidocaine pretreatment also inhibited the depressor response caused by intramuscular formalin (5%;
79 lateral hypothalamus (LH) contributes to the depressor response evoked by somato-visceral nociception
80 t the hypothesis that the vlPAG mediates the depressor response evoked by visceral nociception and in
81 into anesthetized rats elicited a transient depressor response followed by pronounced pressor respon
82 profile and their predominant cardiovascular depressor response to anandamide is mediated through CB(
84 BP (AL=152+/-5; FR=113+/-2 mmHg), less of a depressor response to ganglionic blockade (AL=-58+/-4; F
89 consisting of the Bezold-Jarisch-associated depressor response, a pressor action, and long-lasting d
90 4 had no effect on the endothelin-B-mediated depressor response, whereas SB-209,670 abolished it.
93 s from the lateral column vs. quiescence and depressor responses from the ventrolateral column), rais
94 sion in RA+ mice, we determined the relative depressor responses to intravenous administration of the
95 VLM were functionally defined by pressor and depressor responses to microinjected GABA (500 pmol, 50
96 adycardia, reduction in lumbar SNA, and both depressor responses were equivalent in sham-lesioned and
97 /kg) without cocaine produced dose-dependent depressor responses with recovery typically within 2 hrs
98 eceptors to prevent sympathetically mediated depressor responses, OZRs still had reduced sympathetic
100 giotensin II, and hypoxia; enhance pulmonary depressor responses; and attenuate pulmonary hypertensio
101 his demarcation is not dependent on the anal depressor's intrinsic genetic sex, but is influenced by
103 emical stimulation at identified pressor and depressor sites in the lateral and ventrolateral periaqu
106 ps in the dimorphic re-sculpting of the anal depressor that are regulated by genetic sex and by cell-
108 eas unc-94b is expressed in pharyngeal, anal depressor, vulval and uterine muscles and in spermatheca
109 o address when the changes occur in the anal depressor, we used YFP:actin to monitor, and mutant anal
110 of infection was identified as wooden tongue depressors, which were used on the nursery to construct
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