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1 nds for the scavenger receptor CD36, a major platelet glycoprotein.
2 adhesion molecule-1 (VCAM 1) P-selectin, and platelet glycoprotein-1balpha (GPIbalpha) in the thoraci
4 in a multimerized form, which interacts with platelet glycoproteins and integrins, is a major factor
5 es of vascular damage by binding to specific platelet glycoproteins and to constituents of exposed co
6 dial infarction (UA/NSTEMI) treated with the platelet glycoprotein (Gp IIb/IIIa) inhibitor tirofiban
15 imary hemostasis owing to the absence of the platelet glycoprotein (GP) Ib-IX-V membrane receptor.
17 raction between the amino-terminal domain of platelet glycoprotein (GP) Ibalpha and immobilized von W
23 ntegrin alpha(IIb)beta(3), also known as the platelet glycoprotein (GP) IIb-IIIa complex, mediates pl
24 erfusion, tirofiban, a specific inhibitor of platelet glycoprotein (GP) IIb-IIIa receptors (100 micro
26 as done to determine whether eptifibatide, a platelet glycoprotein (GP) IIb/IIIa antagonist, prevents
30 thin PLNs of ITP, but not controls, abundant platelet glycoprotein (GP) IIb/IIIa autoantigens was fou
31 nd eptifibatide (5 microg/mL), which inhibit platelet glycoprotein (GP) IIb/IIIa but not Mac-1, did n
32 s have been made to evaluate the role of the platelet glycoprotein (GP) IIb/IIIa complex in platelet-
33 ion (PCI) using bivalirudin with provisional platelet glycoprotein (GP) IIb/IIIa inhibition with that
34 ed to receive a double-blind infusion of the platelet glycoprotein (GP) IIb/IIIa inhibitor eptifibati
35 a strategy of upstream use of small molecule platelet glycoprotein (GP) IIb/IIIa inhibitors for all a
36 es have shown a survival benefit with use of platelet glycoprotein (GP) IIb/IIIa inhibitors in diabet
37 I) less than 25 kg/m2 and those treated with platelet glycoprotein (GP) IIb/IIIa inhibitors, in whom
38 ry revascularization who received either the platelet glycoprotein (GP) IIb/IIIa receptor antagonist
42 o-controlled randomized trials of parenteral platelet glycoprotein (GP) IIb/IIIa receptor antagonists
43 ribes the effects of tirofiban, a nonpeptide platelet glycoprotein (GP) IIb/IIIa receptor blocker, on
44 ents with ACS derive particular benefit from platelet glycoprotein (GP) IIb/IIIa receptor inhibition.
45 dogrel, low-molecular-weight heparin (LMWH), platelet glycoprotein (GP) IIb/IIIa receptor inhibitors,
48 ent of a monoclonal antibody directed to the platelet glycoprotein (GP) IIb/IIIa receptor, is a poten
49 inhibitor-1 (PAI-1) [-675] 4G/5G, and three platelet glycoprotein (GP) receptor variants (GPIa C807T
51 dies to fibrin cross-linking factor XIII and platelet glycoprotein (GP)-IIIa to identify fibrin-plate
53 onoclonal antibody 7E3, directed against the platelet glycoprotein (GP)IIb/IIIa receptor, on the char
54 reveals high-affinity antibody (Ab) against platelet glycoprotein (GP)IIIa 49-66, which correlates i
56 intravascular bacteria, a process involving platelet glycoprotein GPIb and bacterial opsonization wi
59 IIb)beta3 (glycoprotein IIb-IIIa) is a major platelet glycoprotein heterodimeric receptor that mediat
61 hemostasis is mediated by interaction of the platelet glycoprotein Ib (GPIb) surface receptor and its
63 ed by absorption with mouse antihuman CD42b [platelet glycoprotein Ib (GPIb)] mAb, had sizes and carg
65 ntibody that inhibits binding of thrombin to platelet glycoprotein Ib inhibits secretory responses to
67 rated that neither von Willebrand factor nor platelet glycoprotein Ib-alpha receptor (GPIb-alpha) is
68 induced by VWF binding to its receptor, the platelet glycoprotein Ib-IX (GPIb-IX), and p38 inhibitor
70 nd factor (vWF)-dependent recruitment of the platelet glycoprotein Ib-IX receptor complex and collage
75 (b)alpha), the ligand binding subunit of the platelet glycoprotein Ib-IX-V complex, is sulfated on th
77 pass (1) platelet rolling via interaction of platelet glycoprotein Ib-IX-V with endothelial-released
78 sease (PT-VWD) is a bleeding disorder of the platelet glycoprotein Ib-IX/von Willebrand factor (VWF)
86 h increase affinity of the VWF A1 domain and platelet glycoprotein Ibalpha (GPIbalpha) for one anothe
87 tion initiation site (Kozak sequence) of the platelet glycoprotein Ibalpha (GPIbalpha) gene was assoc
88 filamin A binding to the cytoplasmic tail of platelet glycoprotein Ibalpha (GpIbalpha) is regulated b
89 ypothesis that VWF may self-associate on the platelet glycoprotein Ibalpha (GpIbalpha) receptor under
90 in, corresponding to the binding site of the platelet glycoprotein Ibalpha (GPIbalpha) receptor, ther
93 xosite I in alpha-thrombin (FIIa) binding to platelet glycoprotein Ibalpha (GPIbalpha), which could i
97 isting of von Willebrand factor (substrate), platelet glycoprotein Ibalpha (receptor), and ADAMTS13 (
98 pe 2B has increased binding affinity between platelet glycoprotein Ibalpha and von Willebrand factor
100 njury, suggesting that a major inhibition of platelet glycoprotein Ibalpha may be beneficial therapy.
101 single VWF A1A2A3 tridomain polypeptides by platelet glycoprotein Ibalpha or antibodies to measure t
102 has been suggested as a counter receptor to platelet glycoprotein Ibalpha that supports initial plat
103 s occurs through transient interactions with platelet glycoprotein Ibalpha via the VWF A1 domain whic
104 rmed on the 16-residue beta-switch region of platelet glycoprotein Ibalpha, for which crystal structu
106 was described to require the VWF receptor on platelets (glycoprotein Ibalpha (GPIbalpha)), the VWF/GP
107 d binding, a primary interaction that allows platelets glycoprotein Ibalpha (GPIbalpha)-induced gener
109 d from ITP patients, 2E7, specific for human platelet glycoprotein IIb heavy chain, and 5E5, specific
112 tes in the design of a novel class of potent platelet glycoprotein IIb-IIIa receptor (GPIIb-IIIa) ant
113 the vitronectin receptor) or alphaIIbbeta3 (platelet glycoprotein IIb-IIIa), and binding was blocked
114 inst platelet surface proteins, particularly platelet glycoprotein IIb/IIIa (alpha(IIb)beta(3)).
115 using a murine monoclonal antibody to human platelet glycoprotein IIB/IIIA (CD41) and immunomagnetic
116 The goal of this study was to test: 1) if platelet glycoprotein IIb/IIIa (GP IIb/IIIa) blockade wi
117 rrent guidelines recommend administration of platelet glycoprotein IIb/IIIa (Gp IIb/IIIa) inhibitors,
120 lacebo-controlled trials testing intravenous platelet glycoprotein IIb/IIIa antagonists in the settin
121 new adjunctive agents and devices, including platelet glycoprotein IIb/IIIa antagonists, primary sten
122 tion (MI) when performed with or without the platelet glycoprotein IIb/IIIa antibody, abciximab.
124 stent deployment and the effect of abciximab platelet glycoprotein IIb/IIIa blockade to improve clini
127 been characterized as a potent and specific platelet glycoprotein IIb/IIIa complex (GPIIb/IIIa) anta
128 IIb/IIIa Inhibitor for STENTing (EPISTENT), Platelet glycoprotein IIb/IIIa in Unstable angina Recept
129 tcomes of 429 patients from 153 sites in the Platelet glycoprotein IIb/IIIa in unstable angina: Recep
130 elet aggregation in patients enrolled in the Platelet glycoprotein IIb/IIIa in Unstable angina: Recep
131 ional, randomized, placebo-controlled trial (Platelet Glycoprotein IIb/IIIa in Unstable Angina: Recep
132 gment elevation ACS who were enrolled in the Platelet Glycoprotein IIb/IIIa in Unstable Angina: Recep
133 /IIIa receptor inhibitor eptifibatide in the Platelet Glycoprotein IIb/IIIa in Unstable Angina: Recep
134 e from the economic substudy of the PURSUIT (Platelet Glycoprotein IIB/IIIA In Unstable Angina: Recep
135 e and tPA for Occluded Arteries (GUSTO)-IIb, Platelet Glycoprotein IIb/IIIa in Unstable Angina: Recep
136 ed Coronary Arteries (GUSTO) IIb, GUSTO-III, Platelet Glycoprotein IIb/IIIa in Unstable Angina: Recep
137 tential of combined fibrinolytic therapy and platelet glycoprotein IIb/IIIa inhibition for improving
138 bosis-II (trial) (IMPACT-II), a trial of the platelet glycoprotein IIb/IIIa inhibitor eptifibatide.
140 device, Angioguard, or double-blind use of a platelet glycoprotein IIb/IIIa inhibitor, abciximab, in
141 and pharmacodynamics of lotrafiban, an oral platelet glycoprotein IIb/IIIa inhibitor, as a secondary
142 in and neutrophil receptor CD11b/CD18, and a platelet glycoprotein IIb/IIIa inhibitor, were incubated
143 ere performed prior to the widespread use of platelet glycoprotein IIb/IIIa inhibitors and intracoron
145 ascularization, agents in the class known as platelet glycoprotein IIb/IIIa inhibitors have significa
146 combination with PTCA, coronary stenting and platelet glycoprotein IIb/IIIa inhibitors may further im
149 target microvascular dysfunction, including platelet glycoprotein IIb/IIIa inhibitors, and agents de
150 t implantation, concurrent administration of platelet glycoprotein IIb/IIIa inhibitors, and the exact
155 ught to determine the efficacy and safety of platelet glycoprotein IIb/IIIa receptor (GP IIb/IIIa) bl
156 ilin Therapy, PURSUIT) demonstrated that the platelet glycoprotein IIb/IIIa receptor antagonist eptif
157 ented a therapeutic benefit for abciximab, a platelet glycoprotein IIb/IIIa receptor antagonist, that
158 -aggregatory effects of currently prescribed platelet glycoprotein IIb/IIIa receptor antagonists duri
159 Although gender differences in response to platelet glycoprotein IIb/IIIa receptor blockade have be
166 tly recommended drug regimens to inhibit the platelet glycoprotein IIb/IIIa receptor have distinct ph
167 afiban, an oral, selective antagonist of the platelet glycoprotein IIb/IIIa receptor in patients stab
168 tion, combination reperfusion therapy with a platelet glycoprotein IIb/IIIa receptor inhibitor (abcix
169 who were randomly assigned to placebo or the platelet glycoprotein IIb/IIIa receptor inhibitor eptifi
170 ve suggested that agents that antagonize the platelet glycoprotein IIb/IIIa receptor may reduce the i
171 ST-segment resolution with higher levels of platelet glycoprotein IIb/IIIa receptor occupancy after
172 eptifibatide may result in higher levels of platelet glycoprotein IIb/IIIa receptor occupancy in the
174 e coronary syndromes results in higher local platelet glycoprotein IIb/IIIa receptor occupancy, which
180 l antibody Fab fragment directed against the platelet glycoprotein IIb/IIIa receptor, has reduced abr
181 ravenous administration of agents that block platelet glycoprotein IIb/IIIa receptors in the setting
182 ibatide, a cyclic heptapeptide antagonist of platelet glycoprotein IIb/IIIa, are substantially altere
183 e, and lamifiban are new agents that inhibit platelet glycoprotein IIb/IIIa, which serves as the fina
186 C resistance and the effect of aspirin and a platelet glycoprotein IIbIIIa antagonist (GR144053F) on
187 8 polymorphism and the Pl(A) polymorphism of platelet glycoprotein IIIa are reported to be independen
188 ociation of the fibrinogen Bbeta 448 and the platelet glycoprotein IIIa Pl(A) polymorphisms in relati
191 t data suggest that the Pl(A2) allele of the platelet glycoprotein IIIa receptor may be a genetic ris
192 ggregation via competitive interactions with platelet glycoprotein integrin receptor GPIIb/IIIa.
195 helium relies on the interaction between the platelet glycoprotein receptor Ib alpha (GPIb(alpha)) an
196 ation of reversible tether bonds between the platelet glycoprotein receptor Ibalpha and the A1 domain
202 roup box 1 (HMGB1) protein, but not membrane platelet glycoprotein VI (GPVI), with dependence on extr
205 promote tight binding of these antibodies to platelet glycoproteins without linking covalently to pro
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