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1 ns within the North American racers (Coluber constrictor).
2 erial pressure imposed by means of an aortic constrictor.
3 al left anterior descending coronary ameroid constrictors.
4 ith infection in ball pythons but not in boa constrictors.
5 imal left circumflex coronary artery ameroid constrictors.
6 d (filmed) predation attempt by an adult Boa constrictor (~ 2 m) on a juvenile white-faced capuchin (
7 as associated with lower RT dose to superior constrictors (37 vs 53 Gy; mean difference, 16 Gy; 95% C
8  of the descending vasa recta as part of its constrictor action and that this vasoconstriction is buf
9                        To study its possible constrictor action, PAF was added to nonpreconstricted E
10   Dermal arterioles displayed no spontaneous constrictor activity in the absence of stimulation.
11 suggest a shift of postinspiratory laryngeal constrictor activity into inspiration.
12 neous blood vessels is mediated by increased constrictor activity of vascular alpha2-adrenoceptors (a
13  displays a normal or enhanced reactivity to constrictor agents as compared with nonrenal circulatory
14 temic vasodilation and hyporesponsiveness to constrictor agents, at a time when the pulmonary circula
15 nd hind limb vascular arterial reactivity to constrictor agonists.
16 ertension and a mouse model of hypertension, constrictor alpha1AR-PKCalpha-TRPV4 signaling was upregu
17  of neurotransmitters and hormones with both constrictor and dilator actions during hibernation are d
18 d concentration-response curves to different constrictor and dilator agonists were obtained at an int
19      The endothelium is involved in both the constrictor and dilator effects of endothelin in rat pul
20  blockade, raising the possibility that both constrictor and dilator fibres are present.
21 is study reports further characterization of constrictor and dilator function in mesenteric and cauda
22 nic responsiveness, together with testing of constrictor and dilator function.
23 arteries were harvested and, in one segment, constrictor and dilator reactivity was determined by wir
24                          Blood pressure, and constrictor and dilator responses in the aorta and mesen
25 ne by sensitizing the smooth muscle cells to constrictor and myogenic stimuli.
26 ciated with proasthmatic-like changes in ASM constrictor and relaxant responsiveness, and that these
27  in turn, evokes proasthmatic changes in ASM constrictor and relaxant responsiveness.
28 exhibited proasthmatic-like changes in their constrictor and relaxation responsiveness that were prev
29                              We infected boa constrictors and ball pythons by cardiac injection of pu
30                              We infected boa constrictors and ball pythons with purified reptarenavir
31 babilities of North American racers (Coluber constrictor) and coachwhips (Coluber flagellum) that ind
32 A2 is a platelet agonist, smooth muscle cell constrictor, and mitogen.
33 s also performed in two pigs with an ameroid constrictor applied to the left circumflex coronary arte
34              Three other groups had arterial constrictors applied to provoke CFVs: group 2 (n=28) rec
35 hemia was induced by placement of an ameroid constrictor around swine left circumflex artery.
36 sly made ischemic by placement of an ameroid constrictor around the circumflex artery.
37 on attempt and published reports of other B. constrictor attacks on primates, the coordinated efforts
38 hat introduced apex predators, such as giant constrictors, can exert significant top-down pressure on
39 rk model, the sensor of the follower pyloric constrictor cell was more informative than the pacemaker
40 via the release of nitric oxide, and have no constrictor component.
41 1 +/- 1.78 vs. CONTROLS: 5.69 +/- 1.56%) and constrictor (CPT %: Athletes: -2.95 +/- 1.07 vs. CONTROL
42                After placement of an ameroid constrictor (day 0) around the left anterior descending
43 el lineage of arenaviruses isolated from boa constrictors diagnosed with IBD.
44                                 The residual constrictor effect observed during AT1 receptor blockade
45  synthase in macula densa cells, reduces the constrictor effect of adenosine, but the regulation of N
46 e contribution of TRPV4(SMC) channels to the constrictor effect of alpha1 adrenergic receptor (alpha1
47 r functional role in the potent long-lasting constrictor effect of endothelin-1 in the cerebral micro
48                               The sum of the constrictor effects exceeds that of the dilator effects
49              Variable venular vs. arteriolar constrictor effects must be considered when evaluating t
50 s characterized by a hypersensitivity to the constrictor effects of endothelin 1 (ET-1).
51         Furthermore, L-arginine reversed the constrictor effects of L-NMMA, indicating that the actio
52 ticoid-inhibitable hyporesponsiveness to the constrictor effects of norepinephrine and abolished symp
53    Estrogen also affects endothelium-derived constrictor factors.
54 chanisms in premucosal vessels with enhanced constrictor forces in inflow vessels.
55 ial impacts on radial artery vasodilator and constrictor function.
56 rts of the swallowing structures: pharyngeal constrictors, glottic and supraglottic larynx, and esoph
57 le increasing NO bioavailability, offsetting constrictor hyper-reactivity and replenishing endothelia
58 scle is best known for its role as an airway constrictor in diseases such as asthma.
59                         Because 15-HETE is a constrictor in this vascular bed, it may play an importa
60 hire swine underwent placement of an ameroid constrictor into the left circumflex artery to induce ch
61  macrophages, and is converted to the potent constrictor LTD(4) and the stable metabolite, LTE(4) .
62 th a time course that suggests a sympathetic constrictor mechanism.
63 y also reduce the proinflammatory effects of constrictor mediators.
64 r the phasic inspiratory activity of glottal constrictor muscle during nasal pressure support ventila
65 n the phasic inspiratory activity of glottal constrictor muscle during nasal pressure support ventila
66 al constrictor muscle or inferior pharyngeal constrictor muscle lying outside the high-dose target vo
67 volume of the superior and middle pharyngeal constrictor muscle or inferior pharyngeal constrictor mu
68  with phasic inspiratory activity of glottal constrictor muscle was measured and compared between the
69 ryngeal motor outputs that control laryngeal constrictor muscles.
70 ated by endothelial-derived vasodilators and constrictors, O2 sensing is intrinsic to ductal smooth m
71              Endothelin-1 (ET-1) is a potent constrictor of bronchial smooth muscle, but there is lim
72              Endothelin-1 (ET1) was a potent constrictor of isolated arterioles and induced a sustain
73 oxyeicosatetraenoic acid (20-HETE), a potent constrictor of pial arterioles.
74 oxyeicosatetraenoic acid (20-HETE), a potent constrictor of the renal and cerebral microcirculation a
75 onstrated the role of endothelin-1 as both a constrictor of uterine myometrial smooth muscle and a pr
76 rticular, by their function as smooth muscle constrictors of airways and microvasculature.
77 five swine underwent placement of an ameroid constrictor on the left circumflex artery.
78 ular systolic dysfunction induced by ameroid constrictors on the coronary arteries, animals were rand
79 al muscles, lips, tongue, palate, pharyngeal constrictors, or smooth and striated muscles of the esop
80 he superior, middle, and inferior pharyngeal constrictor (PC) muscles was examined in 10 normal adult
81 ly more than did the endothelium-independent constrictor phenylephrine (P < .05) despite comparable p
82  of L-NMMA, and in the presence of a control constrictor phenylephrine.
83 ted by successive injections of an hydraulic constrictor placed around the inferior vena cava and mea
84 ated by successive injections of a hydraulic constrictor placed around the inferior vena cava.
85      Chronic ischemia was induced by ameroid constrictor placement around the circumflex artery.
86 ion, chronic ischemia was induced by ameroid constrictor placement around the circumflex coronary art
87 terol diet underwent left circumflex ameroid constrictor placement to induce chronic ischemia at 8 we
88                             Four weeks after constrictor placement, CD31+ mononuclear cells (MNCs) we
89                Twelve dogs underwent ameroid constrictor placement.
90 ngeal elevator thyrohyoid and the pharyngeal constrictors, proved to be different from pharyngeal swa
91  the lateral pyloric (LP) neuron and pyloric constrictor (PY) neuron has an inhibitory depressing che
92 er neurons [lateral pyloric (LP) and pyloric constrictor (PY)] are thought to be primarily responsibl
93 se expression attenuates afferent arteriolar constrictor reactivity and hypertension-induced increase
94 d phenylephrine, but Dex enhanced peripheral constrictor reactivity to endothelin-1.
95 promotes hypertrophic remodelling, increases constrictor reactivity via protein kinase C signalling,
96               In contrast, GoGV-infected boa constrictors remained free of clinical signs for 2 years
97                             In contrast, boa constrictors remained healthy over 2 years, despite high
98 , assessed as the reduction in phenylephrine constrictor response after insulin preincubation, was lo
99 plain why it elicits a monophasic arteriolar constrictor response distinct from the multiphasic dilat
100                We hypothesized that an early constrictor response to acetylcholine, indicative of end
101 amin C markedly depressed the normal femoral constrictor response to acute hypoxaemia in the fetus (5
102 sponse distinct from the multiphasic dilator/constrictor response to adenosine.
103 e controls, an attenuated afferent arteriole constrictor response to endothelin-1 and enhanced dilato
104 elerythrine and staurosporine, decreased the constrictor response to endothelin-1.
105 e in skeletal muscle, but both contribute to constrictor responses evoked by high frequency bursts of
106                                      Venular constrictor responses in OZR were comparable to LZR for
107 found that L-NMMA (1.0 microM) did not alter constrictor responses of the basilar artery in nondiabet
108 o examine the effect of diabetes mellitus on constrictor responses of the basilar artery in vivo.
109  synthesis/release of nitric oxide modulates constrictor responses of the basilar artery to angiotens
110 otential role for nitric oxide in modulating constrictor responses of the basilar artery.
111                          They showed similar constrictor responses to a range of agonists and K+ conc
112 on control diameters in CH or N rats, nor on constrictor responses to air in CH, but reversed or redu
113  endothelium-dependent dilation and enhanced constrictor responses to norepinephrine and the thrombox
114         Endothelial dysfunction and enhanced constrictor responses to norepinephrine were also observ
115             Hypoxia increased uterine artery constrictor responses to norepinephrine, angiotensin II
116 m nitroprusside (SNP; 1 x 10(9)-1 x 10(4)m), constrictor responses to phenylephrine (PE; 1 x 10(9)-1
117                                     However, constrictor responses to UK 14,304, a selective alpha2-A
118 ness, however it is not known if sympathetic constrictor responses vary in men and women.
119 ter vasoreactivity (greater vasodilatory and constrictor responses) than age-matched controls, contri
120 m-sensitized ASM ablated both their enhanced constrictor responsiveness to acetylcholine (ACh) and th
121 tissue with RV induced heightened ASM tissue constrictor responsiveness to acetylcholine and attenuat
122 ell surface expression, and induce increased constrictor responsiveness to acetylcholine and impaired
123      Respiratory-related superior pharyngeal constrictor (SPC) muscle activity was determined in 18 o
124  C(4), LTD(4), and LTE(4), are smooth muscle constrictors that signal via the CysLT(1) receptor.
125 nhibition of these enzymes converted CO from constrictor to dilator.
126 nduced O2*- production and converted CO from constrictor to dilator.
127 day 0) with a hydraulic occluder and ameroid constrictor to enable reversible and gradual total LAD o
128 d increased alpha1 - (and alpha2 -) mediated constrictor tone (collecting).
129           This suggests increased basal ET-1 constrictor tone among obese and type 2 diabetic subject
130  combined effect of ET(A) blockade to reduce constrictor tone and augment dilator tone.
131  normally maximally dilated but have a basal constrictor tone.
132    Using anesthetized dogs, a micromanometer constrictor was applied to either an intact coronary art
133                 Four weeks later, an ameroid constrictor was placed on the left circumflex artery.
134                                      Ameroid constrictors were placed around the proximal coronary ar
135 us (UHV; a virus that we isolated from a Boa constrictor with BIBD) to show that BIBDAV can also repl
136 thelin-1 was the most potent and efficacious constrictor, with a biphasic concentration-response curv

 
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