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1 aled Vwf expression in endothelial cells and thrombocytes.
2  least a 1-fold change relative to unexposed thrombocytes.
3 ch as von Willebrand factor, fibrinogen, and thrombocytes.
4 ates, the functional units of hemostasis are thrombocytes.
5  influence the activity and functionality of thrombocytes.
6 rentiate into erythrocytes, neutrophils, and thrombocytes.
7  with green fluorescent protein (GFP)-tagged thrombocytes.
8 tes as young and DiI- thrombocytes as mature thrombocytes.
9 s and are functionally more active than DiI- thrombocytes.
10 ), monocytes, macrophages, granulocytes, and thrombocytes.
11 ression of VEGFC in both platelets and avian thrombocytes.
12 encoding genes expressed explicitly in young thrombocytes.
13 fish led to an increase in the percentage of thrombocytes.
14 ate dehydrogenase (U/L) x creatinine (mg/dL)/thrombocytes (10(9) cells per L)-termed the Endothelial
15 4,326 gene transcripts were found in chicken thrombocytes across all ligand exposures.
16 ing a detrimental role for infection-induced thrombocyte activation.
17 regate formation, features predicted to make thrombocyte aggregates less resistant than platelets are
18                                    Zebrafish thrombocyte aggregation ex vivo and hemostasis in vivo a
19 for the use of other lipid-lowering therapy, thrombocyte aggregation inhibitors, and antihypertensive
20 al assays, botrocetin promoted VWF-dependent thrombocyte aggregation.
21 n and whole blood clotting without affecting thrombocyte aggregation.
22  modulatory effect of the three microRNAs on thrombocyte aggregation/agglutination.
23                                   Functional thrombocyte analysis using plate tilt assay showed no mo
24 e is one abstract that describes kinetics of thrombocyte and thrombocyte-microparticle recruitment in
25  five factors were shown to be essential for thrombocyte and/or erythroid development in zebrafish.
26              Cells without nuclear DNA, i.e. thrombocytes and hair shafts, only showed the mitotype o
27          Previously, we identified zebrafish thrombocytes and have shown that they participate in art
28  injury from endothelial cells and activated thrombocytes and, therefore, may give rise to acute post
29 ich had the morphologic appearance of mature thrombocytes, and a GFP(low) subset with an immature app
30 nd then selected those that are expressed in thrombocytes, and from this list based on their role in
31                                        Avian thrombocytes are larger than mammalian platelets, spread
32                                              Thrombocytes are the nucleated equivalent of platelets i
33                                              Thrombocytes are thought to arise from bipotent thromboc
34 s, granulocytes, monocytes, lymphocytes, and thrombocytes, are formed through complex genetic signali
35 assified DiI+ thrombocytes as young and DiI- thrombocytes as mature thrombocytes.
36 po mRNA expanded itga2b:GFP(+) (cd41:GFP(+)) thrombocytes as well as hematopoietic stem and progenito
37                           We classified DiI+ thrombocytes as young and DiI- thrombocytes as mature th
38  the functional roles of identified genes in thrombocyte biology may elucidate mechanisms underlying
39 sion in large coronary arteries, circulating thrombocytes, cardiac adipocytes, and outflow tract smoo
40 1/CD42b for the identification of aggregated thrombocytes, CD14/PM-1, and RAM-11 for identification o
41 h formed independent clusters and that young thrombocytes clustered first.
42                                    Zebrafish thrombocytes could be used as a model to study their rol
43 12) cells/L, p = 2.75 x 10(-5)) and elevated thrombocyte count (5.523 [4.862, 6.183] x 10(9) cells/L,
44 phadenopathy (n = 2), lung function (n = 1), thrombocyte counts (n = 1), and chronic enteropathy (n =
45 y correlated with procalcitonin (P = 0.014), thrombocyte counts (P = 0.001), mean platelet volume (P
46 ifies Spi1b as a critical regulator of young thrombocyte development in zebrafish.
47 ays a critical role in supporting T cell and thrombocyte development.
48 nscription factor that potentially regulates thrombocyte development.
49         Here, we recognized 2 populations of thrombocytes distinguishable by DiI-C18 (DiI) staining.
50 in agonists activates the less active mature thrombocytes, drawing them to the growing thrombus.
51 the immune system, leading to endothelia and thrombocyte dysfunction and neurological disease.
52                    We found young and mature thrombocytes each formed independent clusters and that y
53                                              Thrombocytes emerged as the initial Vegfc source during
54 ted 69 CBRP genes from the list of zebrafish thrombocyte-expressed genes.
55 d triggered enhanced Akt phosphorylation and thrombocyte formation.
56   Silencing of nbeal2 in zebrafish abrogated thrombocyte formation.
57 tional role of Tpo in the differentiation of thrombocytes from HSPCs is well conserved among vertebra
58 telet activation could be confirmed in vivo: thrombocytes from mice infected with A. fumigatus showed
59                              Flow sorting of thrombocytes from the mesonephros of adult CD41-GFP zebr
60 CR) signaling, PTEN-loss-driven cancers, and thrombocyte function.
61                                         DiI+ thrombocytes have a high density of adhesive receptors a
62 yte maturation and platelet function because thrombocytes have both megakaryocyte features and platel
63 ngal culture supernatant potently stimulated thrombocytes in a time- and dose-dependent fashion, indu
64                                    Nucleated thrombocytes in fish are activated by collagen but lack
65 chemical pathways reveal the role of chicken thrombocytes in proinflammatory responses linked to key
66                          A reduced number of thrombocytes in the blood (thrombocytopenia) as well as
67  a significantly decreased number of CD41(+) thrombocytes in vivo.
68  study we show that collagen activates trout thrombocytes in whole blood and under flow conditions th
69 s bleeding accompanied by reduced numbers of thrombocytes in zebrafish embryos, recapitulating key as
70                We have also shown that young thrombocytes initiate arterial thrombus formation.
71      These results highlight that Dkk-1 from thrombocytes is an important regulator of leukocyte infi
72 alysis identified 89 tmem genes in zebrafish thrombocytes, leading to further investigation through k
73 ion versus post-administration and, although thrombocyte levels increased (p=0.011), all were within
74 s then silenced, reappearing in the platelet/thrombocyte lineage.
75 t that describes kinetics of thrombocyte and thrombocyte-microparticle recruitment in laser-induced a
76               It is now well understood that thrombocytes (nucleated platelets) express TLRs and resp
77 ke G-CSF, did not impede recovery of HS/PCs, thrombocyte numbers, or glucose metabolism.
78 om their roles in hemostasis and thrombosis, thrombocytes or platelets also promote tumor growth via
79 Cs and niche cells during restoration of the thrombocyte pool.
80 ar inclusions were documented in bone marrow thrombocyte precursors of two young naturally infected d
81 hat it is possible to identify thrombocytes, thrombocyte precursors, and, possibly, early hematopoiet
82 ture appearance, suggesting that they may be thrombocyte precursors.
83                                        While thrombocyte production and aggregation were unaffected,
84 then studied the effect of the 13 targets on thrombocyte production and identified 5 genes, irf5, tgi
85 effects of interleukin-6, a known inducer of thrombocyte production, on globin gene expression during
86 7148, let-7b, and mir-223 are repressors for thrombocyte production.
87  systems like mammals but generate nucleated thrombocytes rather than platelets.
88                     Here, we show that avian thrombocytes respond to many of the same activating stim
89   To deplete platelets, mice were given anti-thrombocyte serum or normal rabbit serum (control) 4 day
90        Platelets were depleted by anti-mouse thrombocyte serum; controls received nonimmunogenic seru
91 ists of Runx1-positive endocardial cells and thrombocytes that induce expression of smooth muscle and
92 increased adhesive receptor density on young thrombocytes, they adhere first to the subendothelial ma
93 s have shown that it is possible to identify thrombocytes, thrombocyte precursors, and, possibly, ear
94 sed to analyze the complete transcriptome of thrombocytes treated with all four microbial products fo
95 ur laboratory, we identified 15 microRNAs in thrombocytes using single-cell RNA sequencing.
96                    Production of circulating thrombocytes was inhibited by the injection of antisense
97  of neutrophils, monocytes, lymphocytes, and thrombocytes were obtained from blood samples.
98 ad diet significantly increased the level of thrombocytes when compared to control bread.
99 bocytopenia by mediating uptake of opsonized thrombocytes, whereas IgM anti-erythrocyte autoantibodie
100 logically relevant collagen receptor in fish thrombocytes which signals through the same ITAM-based s
101 ly, release agonists, and recruit more young thrombocytes, which further release more agonists.

 
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