ライフサイエンスコーパス: cocultivation

1 animals were undetectable in the absence of cocultivation.

2 d Jurkat T reporter cell lines readily after cocultivation.

3 ted with a decrease in embryo response after cocultivation.

4 gments, 56 were already regulated 24 h after cocultivation.

5 ed from infected cells to uninfected ones by cocultivation.

6 ven induced viremias detectable by leukocyte cocultivation.

7 hat were at least as high as transduction by cocultivation.

8 transduced on CH-296 as compared with BSA or cocultivation.

9 sed to transduce murine bone marrow cells by cocultivation.

10 different from that obtained after prolonged cocultivation (24 h, 96 h, and 21 days).

11 ned by varying the germination time prior to cocultivation and altering the bacterium: fungus ratio.

12 produce infectious virus, following explant cocultivation and that spontaneous reactivation could be

13 aponica, cv. Maybelle were explants used for cocultivation, and gene transfer was accomplished using

14 We now show, by using a sensitive cocultivation assay, that these RNA structures and their

15 ype ability to induce syncytia in an XC cell cocultivation assay.

16 vitro with wild-type kinetics in an explant cocultivation assay.

17 Cocultivation assays indicated that the difference in im

18 poor ability to recover infectious virus in cocultivation assays, even after CD8 depletion.

19 ced the amount of fusion observed in XC cell cocultivation assays, suggesting that this region influe

20 Using long term stromal cocultivation assays, we studied the effects of FL on pr

21 n in vivo and in vitro assessed by BMDC OT-I cocultivation assays.

22 e outgrowth of HLA-matched lymphoma cells in cocultivation assays.

23 -dependent signaling during astrocyte-T cell cocultivation by a glutamate uptake inhibitor, l-asparti

24 v-target cell interface only after 30 min of cocultivation, concurrent with the first visible transfe

25 e to transmit the virus to uninfected MDM by cocultivation, confirming the infectiousness of this vir

26 s supernatant on FN 30/35 is as effective as cocultivation directly on producer cells; (2) recombinan

27 In vitro cocultivation experiments provided supporting evidence o

28 In cocultivation experiments, we demonstrate that although

29 hat hyperaccumulate glycogen were assayed by cocultivation experiments.

30 lyzed by plaque assay, PCR, and explantation cocultivation in both immunocompetent and cyclophosphami

31 es persistently upregulated during prolonged cocultivation included three genes (hfq, misR/phoP, and

32 cocci were also upregulated during prolonged cocultivation, indicating that our system models growth

33 EC-ASC cocultivation induced marked accumulation of activin A b

34 Inclusion of L-cysteine in cocultivation medium lead to an improvement in transient

35 A dual-species cocultivation model has been developed by using two ubiq

36 outgrew M2-del(29-31) virus in 4 days after cocultivation of a 100:1 ratio of M2-del(29-31) virus to

37 Cocultivation of ALL cell lines with packaging cell line

38 expression from infections in vivo or during cocultivation of bacteria with tissue culture cells.

39 Cocultivation of cells individually expressing chimerae

40 Cocultivation of CTLs recognizing different CMV epitopes

41 However, cocultivation of EBV-infected B lymphocytes with uninfec

42 equencies of in vitro reactivation following cocultivation of explanted ganglia but reduced frequenci

43 In vitro, cocultivation of hepatocytes and nonparenchymal cells ha

44 ered by direct culture of their urine and by cocultivation of kidney tissue for up to 247 days after

45 que assay or reactivation ex vivo by explant cocultivation of latently infected murine trigeminal gan

46 Cocultivation of lymphocytes from HIV-1-infected persons

47 Cocultivation of lymphoid cell lines with reactivated iS

48 vated from latency following explanation and cocultivation of murine trigeminal ganglia with Vero cel

49 Finally, cocultivation of P. quadriseptata with Arabidopsis enhan

50 tralize primary HIV-1 strains in an assay of cocultivation of peripheral blood mononuclear cells (PBM

51 Cocultivation of primary hepatocytes with a plethora of

52 ation, we adopted and modified the method of cocultivation of single-captured bacterial cells in gel

53 tokine releasing assays were performed after cocultivation of T cells with irradiated Ramos SAg-expre

54 em cells (HSC) is currently only possible by cocultivation of target cells directly on producer cell

55 n the rates of virus reactivation by explant cocultivation of TG from latently infected WT or KO mice

56 Nevertheless, cocultivation of TGN1412-treated T cells with HUVECs ind

57 of gusA transcripts within 18 to 24 hr after cocultivation of the bacteria with either tobacco or mai

58 When virus inhibition was examined after the cocultivation of transduced cells with chronically infec

59 When explant cocultivation of trigeminal ganglia was performed, the v

60 CD38- cells were stimulated with IL-3 during cocultivation on S17 stroma, on fibronectin, or in suspe

61 oviral vectors on CH-296-coated flasks or by cocultivation on vector-producing cells was studied in f

62 A 3-day cocultivation period follows, after which the cultures a

63 gamma nor TNF-alpha were required during the cocultivation period.

64 vidually purified from such a mixed culture (cocultivation) through the use of a combination of a mul

65 Following cocultivation, viral antigens appeared first on PC12 cel

66 Superinfection by either cell-free HIV-1 or cocultivation was blocked.

67 Virus isolation by cocultivation was positive for both CD4+ and CD8+ purifi

68 ould be recovered from the infected PBMCs by cocultivation with a canine indicator cell line, and we

69 heral blood mononuclear cells (PBMC) without cocultivation with a tissue culture cell line.

70 an be successfully transformed using a short cocultivation with A. tumefaciens cells.

71 ncentration for selection is also used after cocultivation with Agrobacterium to mature the transform

72 y regulated (0.5% down-regulated) 48 h after cocultivation with Agrobacterium.

73 An in vitro model of EC cocultivation with ASC was used, in which EC organized i

74 HLA-A2 HAM/TSP patient produced IFN-gamma by cocultivation with autologous CD4 cells, the main reserv

75 ns of primary rat hepatocytes are induced on cocultivation with Chinese hamster ovary cells engineere

76 was determined at intervals during prolonged cocultivation with confluent monolayers of the human res

77 test for PERV infection of human cells after cocultivation with either fetal porcine ventral mesencep

78 uman CD4(+) T cell lines were infected after cocultivation with epithelial cells at both early and la

79 ls and peripheral blood mononuclear cells by cocultivation with freeze-thawed Borrelia burgdorferi sp

80 ciens, and the resultant strain was used for cocultivation with germinated arthroconidia.

81 t infection with cell-free virus, as well as cocultivation with HHV-8-positive primary effusion lymph

82 med, the virus was recovered after 5 days of cocultivation with high efficiency.

83 The viral DNA was infectious, since cocultivation with human corneal fibroblasts (HCF) or hu

84 nd secretion of TNF-alpha was potentiated by cocultivation with IFN-gamma.

85 atant and NK cell supernatant generated from cocultivation with M. tuberculosis-infected monocytes al

86 of therapeutic outcome, while the results of cocultivation with macrophages were of moderate predicti

87 l methods using broth or agar, as well as by cocultivation with macrophages.

88 isolated from infected human cells following cocultivation with miniature swine peripheral blood mono

89 toencapsulation (e.g., double gel, Matrigel, cocultivation with nonparenchymal cells).

90 cted using this technique were transduced by cocultivation with retroviral producers expressing surfa

91 DMDS was depleted from the headspace during cocultivation with seedlings in bipartite Petri dishes,

92 HaCaT monolayers were slightly damaged by cocultivation with strain 35000-3 but this damage was mu

93 The appearance of infectious virus after cocultivation with SupT1 cells was delayed for the provi

94 ing capacity of astrocytes is increased upon cocultivation with T cells.

95 Cocultivation with the virus producer line was consisten