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1  donor's blood samples (both whole blood and platelet-rich plasma).
2 imilar to that observed in vitro using mouse platelet rich plasma.
3 bility to inhibit ADP-induced aggregation in platelet-rich plasma.
4 counts for approximately 20% of total VWF in platelet-rich plasma.
5 DP-induced aggregation of human platelets in platelet-rich plasma.
6 nic acid-induced platelet aggregation in rat platelet-rich plasma.
7 ntent of anandamide in either macrophages or platelet-rich plasma.
8 ergizes with soluble collagen in aggregating platelet-rich plasma.
9 er the stent and was sprayed with autologous platelet-rich plasma adhesive gel.
10   RPAI-1 inhibits in vitro the ADP-dependent platelet-rich plasma aggregation by collagen (COLL), TRA
11                        RPAI-1 inhibits human platelet-rich plasma aggregation triggered by low concen
12 ibition of aggregation of human platelets in platelet rich plasma, an IC50 of 6.8 nM for the inhibiti
13 orn trypsin inhibitor-treated whole blood or platelet rich plasma and subsequent array scanning via a
14 togenous bone and anorganic bovine bone with platelet-rich plasma and a bioabsorbable collagen membra
15 telet aggregation in response to collagen in platelet-rich plasma and firm adhesion on VWF under arte
16 antiplatelet activity both in vitro in human platelet-rich plasma and in vivo in mice.
17                                              Platelet-rich plasma and microneedling have been investi
18 arkedly enhanced thrombin generation in both platelet-rich plasma and platelet-poor plasma, indicatin
19 ysiologically relevant conditions such as in platelet-rich plasma and whole blood.
20 ibition of platelet aggregation in the human platelet rich plasma assay with IC(5)(0) values below 50
21 hat fails to inhibit platelet aggregation in platelet-rich plasma, blocked the inhibitory effect of t
22                      Also, in CypD-deficient platelet-rich plasma, clot retraction was altered.
23 llograft (ADM) to that of a CPT plus ADM and platelet-rich plasma (CPT/PRP) 4 months post-surgically.
24        This study evaluates the influence of platelet-rich plasma derived from bone marrow aspirate (
25 inced the Canadian Blood Services to abandon platelet-rich-plasma-derived concentrates.
26 groups: demineralized freeze dried bone with platelet-rich plasma (DFDB + PRP), DFDB alone, and no tr
27 se of autologous fibrin membrane and the eye platelet-rich plasma (E-PRP) clot could be considered as
28 ncoated stents were then immersed in porcine platelet-rich plasma for two min and the platelet cyclic
29           PT was performed ex vivo by mixing platelet-rich plasma from blood sampling performed at ba
30            Unlike fibrinogen-deficient mice, platelet-rich plasma from Fib(AEK) mice supported normal
31                                     Blood or platelet-rich plasma from healthy volunteers stimulated
32 ated primary glomerular endothelial cells to platelet-rich plasma from patients, or patient platelet-
33 hibited when compared to the wild-type using platelet-rich plasma from the principal donor, but adhes
34 l of PVR in which cells were coinjected with platelet-rich plasma into the vitreous.
35                                              Platelet-rich plasma obtained from healthy (PRP) or tumo
36  of blood microparticles (MPs) obtained from platelet-rich plasma of healthy individuals was characte
37 anufacture of whole-blood-derived platelets (platelet-rich plasma or buffy coat intermediate steps) r
38 Shear-induced GPVI shedding also occurred in platelet-rich plasma or washed platelets isolated from a
39                               Human-citrated platelet-rich plasma or washed platelets were subjected
40                      PMPs were isolated from platelet-rich plasma or were generated by activating was
41 nts or sample volumes can be used, either of platelet-rich plasma or whole blood from human subjects
42 r in agonist-induced aggregation measured in platelet-rich plasma or with washed platelets.
43 ormed in platelets, platelet microparticles, platelet-rich plasma, platelet-poor plasma, and serum.
44  platelet aggregation as measured in a human platelet rich plasma (PRP) assay.
45 th PMN and PMN-RBC combinations suspended in platelet rich plasma (PRP) than in platelet poor plasma
46 played inhibition of platelet aggregation in platelet rich plasma (PRP) with an IC(50) value of 53 nM
47                                           In platelet rich plasma (PRP), progressive APC resistance w
48 ADP stimulated human platelet aggregation in platelet rich plasma (PRP).
49 ration time (TGT) coagulation assay in human platelet rich plasma (PRP).
50 as to evaluate the regenerative influence of platelet-rich plasma (PRP) added to xenogenic bone graft
51 ion of CD62P by wild-type mouse platelets in platelet-rich plasma (PRP) and caused their secretion of
52 procoagulant potential of human platelets in platelet-rich plasma (PRP) and in purified systems.
53 lyze the content and specific effect of both platelet-rich plasma (PRP) and platelet-poor plasma (PPP
54                          The comparison used platelet-rich plasma (PRP) and platelet-poor plasma (PPP
55                                              Platelet-rich plasma (PRP) and platelet-poor plasma (PPP
56              The antimicrobial activities of platelet-rich plasma (PRP) and related plasma preparatio
57 nhanced by 127% (P < 0.001) in study patient platelet-rich plasma (PRP) compared to control PRP and c
58                                              Platelet-rich plasma (PRP) consists of platelet-derived
59                                              Platelet-rich plasma (PRP) contains a number of biologic
60 lcium sulfate hemihydrate (MGCSH) mixed with platelet-rich plasma (PRP) for extraction socket preserv
61                                              Platelet-rich plasma (PRP) from normal mice was able to
62                                              Platelet-rich plasma (PRP) harbors growth factors identi
63                                              Platelet-rich plasma (PRP) has been promoted as a surgic
64 e mineral (NBM) with and without addition of platelet-rich plasma (PRP) has been shown to result in s
65 ch surrounding intra-articular injections of platelet-rich plasma (PRP) has not produced clear eviden
66 hput microfluidic removal of leukocytes from platelet-rich plasma (PRP) in a continuous flow regime.
67 of autologous platelet-rich fibrin (PRF) and platelet-rich plasma (PRP) in the treatment of intrabony
68 al benefits provided by the incorporation of platelet-rich plasma (PRP) into a regenerative protocol
69                                              Platelet-rich plasma (PRP) is a milieu of bioactive fact
70                                              Platelet-rich plasma (PRP) is used to stimulate the repa
71                                              Platelet-rich plasma (PRP) is widely used for many clini
72                                              Platelet-rich plasma (PRP) promotes regeneration of bone
73             Calibrated thrombin assays using platelet-rich plasma (PRP) showed that tissue factor-tri
74 of recalcified platelet-free plasma (PFP) or platelet-rich plasma (PRP) supplemented with corn trypsi
75 al intrabony defects, the benefits of adding platelet-rich plasma (PRP) to a bone replacement graftin
76 plored through a spectrophotometric assay on platelet-rich plasma (PRP) treated with the thromboxane
77                                     Citrated platelet-rich plasma (PRP) turbidimetry is used for asse
78                                              Platelet-rich plasma (PRP) was prepared from 28 healthy
79             Blood samples were collected and platelet-rich plasma (PRP) was prepared.
80 aggregation tests (PATs) were performed with platelet-rich plasma (PRP), a shorter lag time was measu
81                                              Platelet-rich plasma (PRP), an autologous derivative of
82                             A combination of platelet-rich plasma (PRP), bovine porous bone mineral (
83                                              Platelet-rich plasma (PRP), containing autologous growth
84 tomorphometrically analyzes the influence of platelet-rich plasma (PRP), low-level laser therapy (LLL
85 ractionated to yield red blood cells (RBCs), platelet-rich plasma (PRP), platelet-poor plasma (PPP),
86                  Recent reports suggest that platelet-rich plasma (PRP), presumably high in levels of
87                                     In human platelet-rich plasma (PRP), RvE1 selectively blocked bot
88 ng of recombinant human TPO (rhTPO) to human platelet-rich plasma (PRP), washed platelets (WP), and c
89 activation occurred during leukodepletion of platelet-rich plasma (PRP).
90 FXI-depleted plasma and markedly enhanced in platelet-rich plasma (PRP).
91 was modified with PAR4-AP and incubated with platelet-rich plasma (PRP).
92 PVR was induced by the injection of RCFs and platelet-rich plasma (PRP).
93 specifically in VAT, in addition to elevated platelet-rich-plasma (PRP) NPY, compared to control fema
94 12-hydroxyeicosatetraenoic acid to P-12LO-/- platelet-rich plasma rescues the hyperresponsive phenoty
95    Platelet aggregation assays with citrated platelet-rich plasma reveal that the primary and seconda
96 d at baseline in increasing proportions with platelet-rich plasma sampled 4 hours after loading dose.
97 ation, including the use of gene therapy and platelet-rich plasma scaffolds, are also discussed.
98 ing, hydrogel-coated PVC membranes soaked in platelet-rich plasma showed less adhesion and activation
99                                              Platelet-rich plasma showed markedly higher levels of mi
100 ctor Xa-inhibited (250 nM apixaban), diluted platelet rich plasma that had been loaded with the calci
101 ld be prevented by simply reducing the pH of platelet-rich plasma to about 6.5 prior to centrifugatio
102    Using gel-filtered platelets derived from platelet-rich plasma treated with alpha-tocopherol (500
103 r, second-wave aggregation induced by MDC in platelet-rich plasma was inhibited by aspirin, ADP scave
104                                              Platelet-rich plasma was obtained for aggregometry induc
105          Differential levels of endotoxin in platelet-rich plasma were detected using the limulus ame
106  the coagulation cascade in platelet poor or platelet-rich plasma, when activation was initiated by t
107                                  However, in platelet-rich plasma, where formation of both Tx and PGD
108 roparticles in megakaryocyte cultures and in platelet-rich plasma, which are predominantly derived fr
109 atelets derived from apheresis compared with platelet-rich plasma whole-blood-derived platelets.
110 ma cofactor, because a 35-hour incubation of platelet-rich plasma with 125I-factor V showed no specif

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