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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.
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
19 ced the amount of fusion observed in XC cell cocultivation assays, suggesting that this region influe
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
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
36 outgrew M2-del(29-31) virus in 4 days after cocultivation of a 100:1 ratio of M2-del(29-31) virus to
38 expression from infections in vivo or during cocultivation of bacteria with tissue culture cells.
42 equencies of in vitro reactivation following cocultivation of explanted ganglia but reduced frequenci
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
48 vated from latency following explanation and cocultivation of murine trigeminal ganglia with Vero cel
50 tralize primary HIV-1 strains in an assay of cocultivation of peripheral blood mononuclear cells (PBM
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
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
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
64 vidually purified from such a mixed culture (cocultivation) through the use of a combination of a mul
68 ould be recovered from the infected PBMCs by cocultivation with a canine indicator cell line, and we
71 ncentration for selection is also used after cocultivation with Agrobacterium to mature the transform
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
81 t infection with cell-free virus, as well as cocultivation with HHV-8-positive primary effusion lymph
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
88 isolated from infected human cells following cocultivation with miniature swine peripheral blood mono
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
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