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1 ated with increased mRNA expression of VASP (vasodilator-stimulated phosphoprotein).
2 e highly related to Enabled as well as VASP (Vasodilator-Stimulated Phosphoprotein).
3 as an established protein substrate of PKG (vasodilator-stimulated phosphoprotein).
4 activation of cofilin 1 and inactivation of vasodilator-stimulated phosphoprotein.
5 al nitric oxide synthase, and phosphorylated vasodilator-stimulated phosphoprotein.
6 lls and increases the phosphorylation of the vasodilator-stimulated phosphoprotein.
7 ne of these clones was found to encode VASP (vasodilator-stimulated phosphoprotein), a previously ide
8 ICAM-1, and decreased phosphorylation of the vasodilator-stimulated phosphoprotein, a marker for nitr
9 of isoproterenol-induced phosphorylation of vasodilator-stimulated phosphoprotein, a membrane cytosk
11 actin and associated cellular proteins, like vasodilator-stimulated phosphoprotein, adjacent to the a
12 ficantly reduced phosphorylation of platelet vasodilator-stimulated phosphoprotein, an indicator of N
13 3 exposure also led to the redistribution of vasodilator-stimulated phosphoprotein, an NO regulated p
14 A2beta-null cells potentiates Ang II-induced vasodilator-stimulated phosphoprotein and Akt phosphoryl
15 ost actin-regulatory layer containing zyxin, vasodilator-stimulated phosphoprotein and alpha-actinin.
16 partners alpha-actinin and p130Cas, but not vasodilator-stimulated phosphoprotein and cysteine-rich
17 ted exaggerated levels of phosphorylation of vasodilator-stimulated phosphoprotein and extracellular
18 eton-associated proteins including mammalian vasodilator-stimulated phosphoprotein and murine Enabled
19 thromboxane A(2) significantly decreased and vasodilator-stimulated phosphoprotein and nitric oxide i
20 ostanes, and thromboxane A(2), and increased vasodilator-stimulated phosphoprotein and nitric oxide.
21 tivate PKG as measured by phosphorylation of vasodilator-stimulated phosphoprotein, and by in vitro k
22 Enabled, phosphorylated (p)-cortactin, and p-vasodilator-stimulated phosphoprotein, and increased act
23 sured by light transmittance aggregometry or vasodilator-stimulated phosphoprotein assays, was numeri
25 elin-1 may involve Ca(2+), cytoskeleton, and vasodilator-stimulated phosphoprotein changes mediated b
26 encies in actin cytoskeletal organization of vasodilator-stimulated phosphoprotein-containing lamelli
33 ruits host cell Arp2/3 complexes and enabled/vasodilator-stimulated phosphoprotein family members to
34 ave examined the function of a member of the vasodilator-stimulated phosphoprotein family of proteins
35 equently was shown to be a member of the Ena/vasodilator-stimulated phosphoprotein family of proteins
37 ion occurs because of associations involving vasodilator-stimulated phosphoprotein, focal adhesion ki
38 in in response to S-nitrosylation, including vasodilator-stimulated phosphoprotein, focal adhesion ki
39 ion occurs because of associations involving vasodilator-stimulated phosphoprotein, focal adhesion ki
40 es the rapid zyxin-dependent mobilization of vasodilator-stimulated phosphoprotein from focal adhesio
41 nitiation was the gradual coalescence of GFP-vasodilator-stimulated phosphoprotein (GFP-VASP) fluores
42 tions between the C-terminal EVH1 (Ena/VASP [vasodilator-stimulated phosphoprotein] homology domain 1
44 hidonoyl glycerol-induced phosphorylation of vasodilator-stimulated phosphoprotein is mediated by cAM
46 different assays, including VerifyNow P2Y12, vasodilator-stimulated phosphoprotein, light transmittan
47 TPase, peroxisomal farnesylated protein, Ena/vasodilator-stimulated phosphoprotein-like protein, alph
48 let Nox2, Rac1, p47(phox), protein kinase C, vasodilator-stimulated phosphoprotein, nitric oxide, and
53 d or prevented by postsynaptic expression of vasodilator-stimulated phosphoprotein phospho-mimetic or
54 al cyclic adenosine monophosphate (cAMP) and vasodilator-stimulated phosphoprotein phosphorylation (V
56 d IPA was lower and P2Y12 reaction units and vasodilator-stimulated phosphoprotein phosphorylation an
58 (P2Y12 assay) and platelet reactivity index (vasodilator-stimulated phosphoprotein phosphorylation as
59 PD was assessed by using VerifyNow P2Y12 and vasodilator-stimulated phosphoprotein phosphorylation as
60 d significant positive correlations with the vasodilator-stimulated phosphoprotein phosphorylation as
61 denosine diphosphate, VerifyNow P2Y(12), and vasodilator-stimulated phosphoprotein phosphorylation as
62 5 and 20 mumol/l and arachidonic acid), and vasodilator-stimulated phosphoprotein phosphorylation as
63 to dense granules, as confirmed by increased vasodilator-stimulated phosphoprotein phosphorylation in
64 e aggregometry, VerifyNow P2Y(12) assay, and vasodilator-stimulated phosphoprotein phosphorylation in
65 GP) IIb/IIIa after stimulation with ADP, and vasodilator-stimulated phosphoprotein phosphorylation le
66 and PKA, as determined by Rap1 activity and vasodilator-stimulated phosphoprotein phosphorylation, r
67 atment of the cells with kinetics similar to vasodilator-stimulated phosphoprotein phosphorylation.
68 h using light transmission aggregometry and vasodilator-stimulated phosphoprotein phosphorylation.
69 production, cGMP synthesis, and PKG-induced vasodilator-stimulated phosphoprotein phosphorylation.
70 e aggregometry, VerifyNow P2Y(12) assay, and vasodilator-stimulated phosphoprotein phosphorylation.
71 ith different agonists as well as changes in vasodilator-stimulated phosphoprotein platelet reactivit
72 esidual platelet aggregation, p = 0.005) and vasodilator-stimulated phosphoprotein platelet reactivit
73 icantly reduced the effect of clopidogrel on vasodilator-stimulated phosphoprotein platelet reactivit
74 y Artery Bypass Graft (APTITUDE-CABG) study, vasodilator-stimulated phosphoprotein-platelet reactivit
75 e shown to contain the cytoskeletal proteins vasodilator-stimulated phosphoprotein profilin, vinculin
76 the actin-associated proteins alpha-actinin, vasodilator-stimulated phosphoprotein, profilin, Eps8, a
77 ogaster Enabled (Ena) is a member of the Ena/vasodilator-stimulated phosphoprotein protein family, wh
79 1) binding domains of Lpd and the host VASP (vasodilator-stimulated phosphoprotein) recruited to the
80 tream effects, increasing phosphorylation of vasodilator-stimulated phosphoprotein, reducing DNA synt
81 s of the actin-binding protein, cofilin, and vasodilator-stimulated phosphoprotein-regulating conform
82 21680 showed 1) increased phosphorylation of vasodilator-stimulated phosphoprotein that was blocked b
83 l proteins, including the Arp2/3 complex and vasodilator-stimulated phosphoprotein, throughout the ac
84 focal adhesion proteins, including zyxin and vasodilator-stimulated phosphoprotein, undergo retrograd
85 prevented NO-induced phosphorylation of the vasodilator-stimulated phosphoprotein VASP both when NO
86 decrease in PKG-mediated phosphorylation of vasodilator-stimulated phosphoprotein (VASP) and a subse
88 RRs were directly responsible for binding of vasodilator-stimulated phosphoprotein (VASP) and for the
89 d in a time-dependent loss of phosphorylated vasodilator-stimulated phosphoprotein (VASP) and signifi
90 ofilin-actin by the last poly-Pro segment of vasodilator-stimulated phosphoprotein (VASP) and the bin
91 toskeletal substrates for PKA, including the vasodilator-stimulated phosphoprotein (VASP) and the pro
96 le zyxin sequences capable of binding to Ena/vasodilator-stimulated phosphoprotein (VASP) family memb
97 associates with members of the Enabled (Ena)/vasodilator-stimulated phosphoprotein (VASP) family of c
98 more recently, as a member of the Ena/human vasodilator-stimulated phosphoprotein (VASP) family of p
99 (SH3), WW, GYF, and Drosophila enabled (Ena)/vasodilator-stimulated phosphoprotein (VASP) homology 1
100 oncentrations nor induced phosphorylation of vasodilator-stimulated phosphoprotein (VASP) in washed h
104 (NO) synthase (eNOS)/protein kinase G (PKG)/vasodilator-stimulated phosphoprotein (VASP) pathway.
109 rovide genetic and biochemical evidence that vasodilator-stimulated phosphoprotein (VASP) recruitment
110 ow the multifunctional actin-binding protein vasodilator-stimulated phosphoprotein (VASP) regulates t
111 n this study, we sought to determine whether vasodilator-stimulated phosphoprotein (VASP) signaling i
112 us sequence = FE(D)FPPPPTD(E)E(D)] to tether vasodilator-stimulated phosphoprotein (VASP) to the bact
113 e L. monocytogenes strains unable to recruit vasodilator-stimulated phosphoprotein (VASP) to their su
114 ctin (F-actin) and of the signaling molecule vasodilator-stimulated phosphoprotein (VASP) was measure
115 rylation and intracellular redistribution of vasodilator-stimulated phosphoprotein (VASP), a critical
116 were induced by macrophage overexpression of vasodilator-stimulated phosphoprotein (VASP), a key down
118 hances the phosphorylation at Ser-239 of the vasodilator-stimulated phosphoprotein (VASP), a major su
119 expression and phosphorylation state of the vasodilator-stimulated phosphoprotein (VASP), a membrane
120 by AE33 shares similarity with the mammalian vasodilator-stimulated phosphoprotein (VASP), a substrat
121 Microsequencing identified this protein as vasodilator-stimulated phosphoprotein (VASP), an actin b
122 that the actin polymerizing proteins Arp2/3, vasodilator-stimulated phosphoprotein (VASP), and neural
123 lation of actin-based propulsion require the vasodilator-stimulated phosphoprotein (VASP), which bind
130 oteins including the Ena/VASP family member, vasodilator-stimulated phosphoprotein (VASP); however, a
132 lls transfected with the cGKII phosphorylate vasodilator-stimulated phosphoprotein, VASP, after cGMP
134 Ras homolog gene family member A (RhoA) and vasodilator-stimulated phosphoprotein was increased in r
135 k was released, whereas a novel complex with vasodilator-stimulated phosphoprotein was stimulated.
136 aramagnetic resonance and phosphorylation of vasodilator-stimulated phosphoprotein were determined.
137 rotein kinase A (PKA), and the PKA substrate vasodilator-stimulated phosphoprotein were involved in A
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