ライフサイエンスコーパス: thrombocyte

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 ate dehydrogenase (U/L) x creatinine (mg/dL)/thrombocytes (10(9) cells per L)-termed the Endothelial

12 4,326 gene transcripts were found in chicken thrombocytes across all ligand exposures.

13 regate formation, features predicted to make thrombocyte aggregates less resistant than platelets are

14 Zebrafish thrombocyte aggregation ex vivo and hemostasis in vivo a

15 for the use of other lipid-lowering therapy, thrombocyte aggregation inhibitors, and antihypertensive

16 al assays, botrocetin promoted VWF-dependent thrombocyte aggregation.

17 e is one abstract that describes kinetics of thrombocyte and thrombocyte-microparticle recruitment in

18 five factors were shown to be essential for thrombocyte and/or erythroid development in zebrafish.

19 Previously, we identified zebrafish thrombocytes and have shown that they participate in art

20 injury from endothelial cells and activated thrombocytes and, therefore, may give rise to acute post

21 ich had the morphologic appearance of mature thrombocytes, and a GFP(low) subset with an immature app

22 Avian thrombocytes are larger than mammalian platelets, spread

23 Thrombocytes are the nucleated equivalent of platelets i

24 Thrombocytes are thought to arise from bipotent thromboc

25 s, granulocytes, monocytes, lymphocytes, and thrombocytes, are formed through complex genetic signali

26 assified DiI+ thrombocytes as young and DiI- thrombocytes as mature thrombocytes.

27 po mRNA expanded itga2b:GFP(+) (cd41:GFP(+)) thrombocytes as well as hematopoietic stem and progenito

28 We classified DiI+ thrombocytes as young and DiI- thrombocytes as mature th

29 1/CD42b for the identification of aggregated thrombocytes, CD14/PM-1, and RAM-11 for identification o

30 h formed independent clusters and that young thrombocytes clustered first.

31 ays a critical role in supporting T cell and thrombocyte development.

32 Here, we recognized 2 populations of thrombocytes distinguishable by DiI-C18 (DiI) staining.

33 in agonists activates the less active mature thrombocytes, drawing them to the growing thrombus.

34 the immune system, leading to endothelia and thrombocyte dysfunction and neurological disease.

35 We found young and mature thrombocytes each formed independent clusters and that y

36 d triggered enhanced Akt phosphorylation and thrombocyte formation.

37 Silencing of nbeal2 in zebrafish abrogated thrombocyte formation.

38 tional role of Tpo in the differentiation of thrombocytes from HSPCs is well conserved among vertebra

39 telet activation could be confirmed in vivo: thrombocytes from mice infected with A. fumigatus showed

40 Flow sorting of thrombocytes from the mesonephros of adult CD41-GFP zebr

41 CR) signaling, PTEN-loss-driven cancers, and thrombocyte function.

42 DiI+ thrombocytes have a high density of adhesive receptors a

43 ngal culture supernatant potently stimulated thrombocytes in a time- and dose-dependent fashion, indu

44 Nucleated thrombocytes in fish are activated by collagen but lack

45 chemical pathways reveal the role of chicken thrombocytes in proinflammatory responses linked to key

46 study we show that collagen activates trout thrombocytes in whole blood and under flow conditions th

47 s bleeding accompanied by reduced numbers of thrombocytes in zebrafish embryos, recapitulating key as

48 We have also shown that young thrombocytes initiate arterial thrombus formation.

49 These results highlight that Dkk-1 from thrombocytes is an important regulator of leukocyte infi

50 s then silenced, reappearing in the platelet/thrombocyte lineage.

51 t that describes kinetics of thrombocyte and thrombocyte-microparticle recruitment in laser-induced a

52 It is now well understood that thrombocytes (nucleated platelets) express TLRs and resp

53 ke G-CSF, did not impede recovery of HS/PCs, thrombocyte numbers, or glucose metabolism.

54 ar inclusions were documented in bone marrow thrombocyte precursors of two young naturally infected d

55 hat it is possible to identify thrombocytes, thrombocyte precursors, and, possibly, early hematopoiet

56 ture appearance, suggesting that they may be thrombocyte precursors.

57 effects of interleukin-6, a known inducer of thrombocyte production, on globin gene expression during

58 systems like mammals but generate nucleated thrombocytes rather than platelets.

59 Here, we show that avian thrombocytes respond to many of the same activating stim

60 To deplete platelets, mice were given anti-thrombocyte serum or normal rabbit serum (control) 4 day

61 Platelets were depleted by anti-mouse thrombocyte serum; controls received nonimmunogenic seru

62 increased adhesive receptor density on young thrombocytes, they adhere first to the subendothelial ma

63 s have shown that it is possible to identify thrombocytes, thrombocyte precursors, and, possibly, ear

64 sed to analyze the complete transcriptome of thrombocytes treated with all four microbial products fo

65 Production of circulating thrombocytes was inhibited by the injection of antisense

66 ad diet significantly increased the level of thrombocytes when compared to control bread.

67 bocytopenia by mediating uptake of opsonized thrombocytes, whereas IgM anti-erythrocyte autoantibodie

68 logically relevant collagen receptor in fish thrombocytes which signals through the same ITAM-based s

69 ly, release agonists, and recruit more young thrombocytes, which further release more agonists.