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1  infusion of methacholine chloride (Mch), an endothelium-dependent vasodilator.
2 mulative administration of acetylcholine, an endothelium-dependent vasodilator.
3 itric oxide bioavailability at rest and with endothelium-dependent vasodilators.
4 t K(IR) channels function as 'amplifiers' of endothelium-dependent vasodilators.
5 ty and preserves renal vascular responses to endothelium-dependent vasodilators.
6 at rest, during exercise, and in response to endothelium-dependent vasodilators.
7 n produced by neocortical application of the endothelium-dependent vasodilator acetylcholine (10 micr
8 r changes were determined in response to the endothelium-dependent vasodilator acetylcholine (ACh, 10
9 nses to intra-arterial administration of the endothelium-dependent vasodilator acetylcholine (P=0.03)
10 n during intracoronary administration of the endothelium-dependent vasodilator acetylcholine and the
11       Coronary blood flow in response to the endothelium-dependent vasodilator acetylcholine as well
12  threshold dose of genistein potentiated the endothelium-dependent vasodilator acetylcholine but not
13                                          The endothelium-dependent vasodilator acetylcholine elicited
14 n but did not ameliorate the response to the endothelium-dependent vasodilator acetylcholine.
15 d by neural activity, hypercapnia, or by the endothelium-dependent vasodilator acetylcholine.
16 ndothelial cell function was assessed by the endothelium-dependent vasodilator acetylcholine.
17 cterized by vasoconstrictive response to the endothelium-dependent vasodilator acetylcholine.
18 coronary vasoconstriction in response to the endothelium-dependent vasodilator acetylcholine.
19 ) were calculated during (1) infusion of the endothelium-dependent vasodilators acetylcholine (ACh) a
20 008), Responses of resistance vessels to the endothelium-dependent vasodilators acetylcholine and ADP
21                        Dose responses for an endothelium-dependent vasodilator, acetylcholine (ACh, v
22                    Elevation of IP(3) by the endothelium-dependent vasodilator, acetylcholine, increa
23 absolute forearm blood-flow responses to the endothelium-dependent vasodilator, acetylcholine, increa
24 renergic receptor agonist, phenylephrine; b) endothelium-dependent vasodilator, acetylcholine; and c)
25 ents the impaired vascular relaxation to the endothelium-dependent vasodilator ACh, this agent may be
26 ion responses of precontracted arterioles to endothelium-dependent vasodilators adenosine 5'-diphosph
27 ter 2 hours of reperfusion, but those to the endothelium-dependent vasodilator ADP and the endotheliu
28 alpha(1) -agonist) during (i) infusion of an endothelium-dependent vasodilator alone (Protocol 1: ACh
29 tudies show that apelin receptor ligands are endothelium-dependent vasodilators and potent inotropes,
30 cetylcholine (7.5, 15 and 30 microg/min), an endothelium-dependent vasodilator, and sodium nitropruss
31 in) and bradykinin (BK, 2.5 micrograms/min), endothelium-dependent vasodilators, and sodium nitroprus
32      Although responses to acetylcholine, an endothelium-dependent vasodilator, are abnormal in patie
33                                 Responses to endothelium-dependent vasodilators, both in resistance v
34 /min), SLIGKV (160 to 800 nmol/min), and the endothelium-dependent vasodilator bradykinin (100 to 100
35                            Relaxation to the endothelium-dependent vasodilator bradykinin was decreas
36 cid (LPA) has been recognized recently as an endothelium-dependent vasodilator, but several lines of
37      Similar to Ercc1(d/-) mice, age-related endothelium-dependent vasodilator dysfunction in Xpd(TTD
38 ate that blockade of ET-1 receptors improves endothelium-dependent vasodilator function in hypertensi
39                                        Since endothelium-dependent vasodilator function may be affect
40 n of increased ET-1 activity to the impaired endothelium-dependent vasodilator function of hypertensi
41 e and that this is associated with a reduced endothelium-dependent vasodilator function, endothelium-
42 s to acetylcholine and in vitro responses to endothelium-dependent vasodilators in angiotensin II-tre
43  sepiapterin or MH4 restores the response to endothelium-dependent vasodilators in pig coronary arter
44 ctors, indicating that the reduced effect of endothelium-dependent vasodilators in those with hyperte
45 blood flow elicited by neural activity or by endothelium-dependent vasodilators in WT mice but not in
46                       Response of IP(DVP) to endothelium-dependent vasodilators may provide a measure
47  graded intrafemoral artery infusions of the endothelium-dependent vasodilator methacholine chloride
48  graded intrafemoral artery infusions of the endothelium-dependent vasodilator methacholine chloride
49  graded intrafemoral artery infusions of the endothelium-dependent vasodilator methacholine chloride
50  graded intrafemoral artery infusions of the endothelium-dependent vasodilator methacholine chloride
51  response to norepinephrine, and an impaired endothelium-dependent vasodilator response to acetylchol
52 erhomocyst(e)inemic mice restored the normal endothelium-dependent vasodilator response.
53                                              Endothelium-dependent vasodilator responses to acetychol
54 t with apo A-I(M)/PC prevented impairment of endothelium-dependent vasodilator responses to acetylcho
55 on and no impairments in vasoconstrictor and endothelium-dependent vasodilator responses, associated
56 amin E therapies similarly improved arterial endothelium-dependent vasodilator responsiveness consist
57  lipoprotein levels, specific improvement in endothelium-dependent vasodilator responsiveness is simi
58 ange in augmentation index in response to an endothelium-dependent vasodilator (salbutamol).
59 nd dilated in a dose-dependent manner to the endothelium-dependent vasodilators serotonin, ATP, and i
60  coronary artery constriction in response to endothelium-dependent vasodilator stimuli such as the co
61 w responses to intrabrachial infusion of the endothelium-dependent vasodilators substance P and acety
62 IK(Ca)/SK(Ca)), NS309 (10(-5) M), and to the endothelium-dependent vasodilators, substance P (10(-8)
63                                              Endothelium-dependent vasodilators, such as acetylcholin
64 roxide production and the response to either endothelium-dependent vasodilator used.
65  systemic vascular reactivity in response to endothelium-dependent vasodilators, which may be mediate
66 , we hypothesized that the responsiveness to endothelium-dependent vasodilators would be greater in t