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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
3     Cartilage intermediate layer protein and platelet glycoprotein 4 (CD36) were identified as having
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
7  a locus immediately adjacent to that of the platelet glycoprotein (GP) Ib b.
8                                    An absent platelet glycoprotein (GP) Ib-IX receptor results in the
9                    We have reconstituted the platelet glycoprotein (GP) Ib-IX-mediated activation of
10                      The interaction between platelet glycoprotein (GP) Ib-IX-V complex and von Wille
11                                          The platelet glycoprotein (GP) Ib-IX-V complex is the recept
12                                          The platelet glycoprotein (GP) Ib-IX-V complex mediates the
13                       The interaction of the platelet glycoprotein (GP) Ib-IX-V complex with von Will
14 duced platelet aggregation by binding to the platelet glycoprotein (GP) Ib-IX-V complex.
15 imary hemostasis owing to the absence of the platelet glycoprotein (GP) Ib-IX-V membrane receptor.
16                      Shear stress causes the platelet glycoprotein (Gp) Ib/IX/V to bind to von Willeb
17 raction between the amino-terminal domain of platelet glycoprotein (GP) Ibalpha and immobilized von W
18                           We have identified platelet glycoprotein (GP) Ibalpha as a counterreceptor
19 tion between von Willebrand factor (VWF) and platelet glycoprotein (GP) Ibalpha.
20 uced brain injury in response to blockade of platelet glycoprotein (GP) Ibalpha.
21 erties regulating A1 domain interaction with platelet glycoprotein (GP) Ibalpha.
22 n the alphaMI domain as the binding site for platelet glycoprotein (GP) Ibalpha.
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
25                         Interactions between platelet glycoprotein (Gp) IIb/IIIa and plasma proteins
26 as done to determine whether eptifibatide, a platelet glycoprotein (GP) IIb/IIIa antagonist, prevents
27                                              Platelet glycoprotein (GP) IIb/IIIa antagonists are indi
28                                              Platelet glycoprotein (GP) IIb/IIIa antagonists prevent
29                       Monoclonal anti-rabbit platelet glycoprotein (GP) IIb/IIIa antibody (AZ1) was a
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
39                                          The platelet glycoprotein (GP) IIb/IIIa receptor antagonist
40                                              Platelet glycoprotein (GP) IIb/IIIa receptor antagonists
41                                      Several platelet glycoprotein (GP) IIb/IIIa receptor antagonists
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,
46                                          The platelet glycoprotein (GP) IIb/IIIa receptor is importan
47                                          The platelet glycoprotein (GP) IIb/IIIa receptor is the fina
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
50                                              Platelet glycoprotein (GP) VI is a 62-kDa membrane glyco
51 dies to fibrin cross-linking factor XIII and platelet glycoprotein (GP)-IIIa to identify fibrin-plate
52  a quantitative or qualitative defect in the platelet glycoprotein (GP)Ib/IX complex.
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
55                                           In platelets, glycoprotein (GP)Ib-IX receptor complex has b
56  intravascular bacteria, a process involving platelet glycoprotein GPIb and bacterial opsonization wi
57               Immunofluorescence staining of platelet glycoprotein GPIbalpha and fibrin(ogen) reveale
58                                          The platelet glycoproteins (GPs) Ib, integrin alpha(2)beta(1
59 IIb)beta3 (glycoprotein IIb-IIIa) is a major platelet glycoprotein heterodimeric receptor that mediat
60                                          The platelet glycoprotein Ib (GpIb) complex is composed of f
61 hemostasis is mediated by interaction of the platelet glycoprotein Ib (GPIb) surface receptor and its
62 ediates platelet adhesion through binding to platelet glycoprotein Ib (GPIb).
63 ed by absorption with mouse antihuman CD42b [platelet glycoprotein Ib (GPIb)] mAb, had sizes and carg
64                          Mutations in VWF or platelet glycoprotein Ib can either reduce or increase t
65 ntibody that inhibits binding of thrombin to platelet glycoprotein Ib inhibits secretory responses to
66                                              Platelet glycoprotein Ib, T-cell receptor, and integrins
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
69                                          The platelet glycoprotein Ib-IX receptor binds surface-bound
70 nd factor (vWF)-dependent recruitment of the platelet glycoprotein Ib-IX receptor complex and collage
71 idge between subendothelial collagen and the platelet glycoprotein Ib-IX-V complex (GPIb).
72                                          The platelet glycoprotein Ib-IX-V complex (GPIb-IX-IV) is th
73                                          The platelet glycoprotein Ib-IX-V complex plays critical rol
74                                          The platelet glycoprotein Ib-IX-V complex plays crucial role
75 (b)alpha), the ligand binding subunit of the platelet glycoprotein Ib-IX-V complex, is sulfated on th
76         This process requires the binding of platelet glycoprotein Ib-IX-V to the A1 domain of VWF mo
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)
79  for interaction with a peptide derived from platelet glycoprotein Ib.
80 A1 domain that mediates vWF interaction with platelet glycoprotein Ib.
81 upported platelet binding, which depended on platelet glycoprotein Ib.
82 ypes I and III but also decreased binding to platelet glycoproteins Ib and IIbIIIa.
83                    Domains A1 and A3 bind to platelet glycoprotein Ibalpha (GPIbalpha) and collagen,
84                 The adhesion was mediated by platelet glycoprotein Ibalpha (GPIbalpha) because the ad
85          We have determined the structure of platelet glycoprotein Ibalpha (GpIbalpha) bound to throm
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
91  von Willebrand factor binding region of the platelet glycoprotein Ibalpha (GPIbalpha) subunit.
92                                   Binding of platelet glycoprotein Ibalpha (GPIbalpha) to von Willebr
93 xosite I in alpha-thrombin (FIIa) binding to platelet glycoprotein Ibalpha (GPIbalpha), which could i
94 : the von Willebrand factor (VWF) binding to platelet glycoprotein Ibalpha (GPIbalpha).
95 ebrand factor (VWF) regulates the binding to platelet glycoprotein Ibalpha (GPIbalpha).
96  and mediates the adhesion of neutrophils to platelet glycoprotein Ibalpha (GPIbalpha).
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
99      These cells expressed alphaIIbbeta3 and platelet glycoprotein Ibalpha but were devoid of hematop
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
105  not a strict requirement for VWF binding to platelet glycoprotein Ibalpha.
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
108                                          The platelet glycoprotein IIb (alpha(IIb); CD41) constitutes
109 d from ITP patients, 2E7, specific for human platelet glycoprotein IIb heavy chain, and 5E5, specific
110             In contrast, epinephrine-induced platelet glycoprotein IIb-IIIa expression increased afte
111                                          The Platelet Glycoprotein IIb-IIIa in Unstable Angina: Recep
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,
118                 Parenteral administration of platelet glycoprotein IIb/IIIa (GP IIb/IIIa) receptor bl
119               Pharmacodynamic effects of the platelet glycoprotein IIb/IIIa antagonist eptifibatide h
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.
123       However, the efficacy of stenting with platelet glycoprotein IIb/IIIa blockade has not yet been
124 stent deployment and the effect of abciximab platelet glycoprotein IIb/IIIa blockade to improve clini
125                                              Platelet glycoprotein IIb/IIIa blockade with abciximab (
126           Lotrafiban, an orally administered platelet glycoprotein IIb/IIIa blocker, induced a 33% in
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.
139 rst in vivo study of combination intravenous platelet glycoprotein IIb/IIIa inhibitor therapy.
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
144                                    Trials of platelet glycoprotein IIb/IIIa inhibitors as adjuncts to
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
147                   Although many believe that platelet glycoprotein IIb/IIIa inhibitors should be used
148           Stents were used in 12 trials, and platelet glycoprotein IIb/IIIa inhibitors were used in e
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
151                           To date, the other platelet glycoprotein IIb/IIIa inhibitors, including Int
152 VUS imaging in the era before routine use of platelet glycoprotein IIb/IIIa inhibitors.
153                                              Platelet glycoprotein IIb/IIIa is a membrane receptor fo
154                       Monoclonal antibody to platelet glycoprotein IIb/IIIa receptor (7E3) has been s
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
160             Previous work has suggested that platelet glycoprotein IIb/IIIa receptor blockade may con
161        We sought to determine the effects of platelet glycoprotein IIb/IIIa receptor blockade on adve
162                                              Platelet glycoprotein IIb/IIIa receptor blockade with ep
163                                   The use of platelet glycoprotein IIb/IIIa receptor blockers did not
164          Clinical benefit was seen even when platelet glycoprotein IIb/IIIa receptor blockers were ad
165                            Inhibitors of the platelet glycoprotein IIb/IIIa receptor given intravenou
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
173                                              Platelet glycoprotein IIb/IIIa receptor occupancy was si
174 e coronary syndromes results in higher local platelet glycoprotein IIb/IIIa receptor occupancy, which
175                        Thus, blockade of the platelet glycoprotein IIb/IIIa receptor reduces ischemic
176                              Blockade of the platelet glycoprotein IIb/IIIa receptor with abciximab (
177                            Inhibition of the platelet glycoprotein IIb/IIIa receptor with abciximab,
178                              Blockade of the platelet glycoprotein IIb/IIIa receptor with the monoclo
179                            Inhibition of the platelet glycoprotein IIb/IIIa receptor with the monoclo
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
184 rt-acting inhibitor of fibrinogen binding to platelet glycoprotein IIb/IIIa.
185                      Thermal denaturation of platelet glycoprotein IIbIIIa (integrin alpha IIb beta 3
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
189                                          The platelet glycoprotein IIIa Pl(A2) polymorphism and the f
190                        The gene encoding the platelet glycoprotein IIIa receptor (GPIIIa), shows poly
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.
193 dent antibodies (DDAbs) that bind tightly to platelet glycoproteins only when drug is present.
194                                              Platelet glycoprotein polymorphisms should be added to t
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
197               In this study we show that two platelet glycoprotein receptors that signal via an immun
198 nalysis suggested a link between the VLR and platelet glycoprotein receptors.
199                                              Platelet glycoprotein VI (GPVI) interacts with collagen
200                                              Platelet glycoprotein VI (GPVI) is a key receptor for co
201 nvestigated whether TULA-2 has a key role in platelet glycoprotein VI (GPVI) signaling.
202 roup box 1 (HMGB1) protein, but not membrane platelet glycoprotein VI (GPVI), with dependence on extr
203                       PDE levels of PDGF-AA, platelet glycoprotein VI, integrin-linked kinase-1, high
204 reas PDEs had significantly higher levels of platelet glycoprotein VI.
205 promote tight binding of these antibodies to platelet glycoproteins without linking covalently to pro

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