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1 res were correctly identified (including one mixed culture).
2 nocytes to produce inflammatory cytokines in mixed culture.
3 for the direct identification of isolates in mixed culture.
4 ination of cancer cells from healthy ones in mixed culture.
5 smission or new infection events in cells in mixed culture.
6 the robust methylation efficiencies in this mixed culture.
7 mccartyi biomarkers in a well-characterized mixed culture.
8 stradiol (EE(2)) under aerobic conditions in mixed culture.
9 ncreasing the proportion of swarmer cells in mixed culture.
10 xed culture requires its separation from the mixed culture.
11 metabolic fluxes of targeted organisms in a mixed culture.
12 antify the frequencies of pairs of clones in mixed culture.
13 sing the same stimuli that were effective in mixed cultures.
14 t gram-negative bacteria in 12 of 41 (29.3%) mixed cultures.
15 isms and to isolate individual colonies from mixed cultures.
16 signal that mediates appropriate matching in mixed cultures.
17 hibited a modest replication disadvantage in mixed cultures.
18 d and easy to interpret and may be used with mixed cultures.
19 olony is possible, allowing the screening of mixed cultures.
20 ory setting when microorganisms are grown as mixed cultures.
21 use of technical difficulties in maintaining mixed cultures.
22 om both pure isolates and samples containing mixed cultures.
23 ns, which is in line with data obtained from mixed cultures.
24 with conventional bulk measurements of EBPR mixed cultures.
25 hurdle for isotopomer-based flux analysis of mixed cultures.
26 ion induces loss of self-renewing cells from mixed cultures.
27 ation for 400 single-pathogen cultures and 9 mixed cultures.
31 r, inhibition of astrocytic NFAT activity in mixed cultures ameliorated Abeta-dependent elevations in
32 obial biology arose in the context of a very mixed culture and cannot be understood without unscrambl
33 ion for these microbes, even when growing in mixed culture and utilizing a shared substrate which has
35 how that individual species or serovars in a mixed culture are identifiable among a biological VOC ba
45 ta indicate that nearly all neurons in these mixed cultures can undergo apoptosis in response to appr
47 ins can be individually purified from such a mixed culture (cocultivation) through the use of a combi
49 The mice were injected subcutaneously with mixed cultures containing Escherichia coli, Bacteroides
50 V-JHM, and MHV-A59/MHV-JHM) were passaged in mixed cultures containing progressively increasing conce
54 distributed relative to themselves, but, in mixed culture, each predator clusters around its respect
56 e in suppressing E. coli in these planktonic mixed cultures, even though PEf1 reached higher concentr
57 her reports of cooperative invasion in which mixed cultures exhibit a follow-the-leader mechanism, we
60 such as acetate are easily produced through mixed culture fermentation of many biological waste stre
61 uction of fine chemicals following undefined mixed culture fermentation, embedding carbon in industri
63 olation of Candida species either in pure or mixed culture from intraoperatively collected abdominal
64 mpeted by B. animalis subsp. lactis Bl-04 in mixed cultures growing on raffinose, the preferred ligan
65 ed monochloramine cometabolism by nitrifying mixed cultures grown under more relevant drinking water
67 e, studies of bacterial pathogenesis in well-mixed cultures have revealed virulence factors and the r
70 the responses of fresh control CD4+ cells in mixed cultures indicating that the apparent "anergy" was
71 uppress the response of naive CD4 T cells in mixed cultures, indicating that this tolerance mechanism
73 nin, on which astrocytes overgrow neurons in mixed cultures, laminin-coated soft gels encourage attac
76 a series of continuously fed dechlorinating mixed-culture microcosm experiments (n = 26), we varied
77 wever, when grown in MOPS minimal medium, in mixed cultures, more hmp mutant cells were recovered tha
78 nown target and two hypersensitive loci in a mixed culture of 233 strains in the presence of the drug
80 this inflammatory neurodegeneration using a mixed culture of neurons, microglia, and astrocytes, eit
82 s using an anaerobic bioreactor containing a mixed culture of sulfate-reducing bacteria which precipi
83 d DA cell death in mesencephalic neuron-glia mixed culture of wild-type (WT) mice, but this was atten
87 y from inoculated medium, sterile swabs, and mixed cultures of C. jejuni and coliform bacteria were t
88 This capability plus the ability to detect mixed cultures of Candida spp. promises to improve and s
89 n of Th1 and Th2 cytokines in OVA-stimulated mixed cultures of CD4(+) T cells from Tpl2(+/+)/OT2 or T
93 s of neurodegeneration/neuroprotection using mixed cultures of cortical cells challenged with beta-am
94 ection against excitotoxic neuronal death in mixed cultures of cortical cells; and 3) protection agai
96 f isolated crest-derived cells but did so in mixed cultures of crest- and non-neural crest-derived ce
98 y to show that TGFbeta promotes migration in mixed cultures of embryonic sclerotome and associated me
100 a shift in excitation/inhibition balance in mixed cultures of hippocampal neurons exposed to SAVAs.
103 but unlike GLT-1, the addition of dbcAMP to mixed cultures of neurons and astrocytes caused GLAST pr
104 GLT-1 protein, but the addition of dbcAMP to mixed cultures of neurons and astrocytes did not cause G
114 bolic flux analysis of a given organism in a mixed culture requires its separation from the mixed cul
115 coexistence between the two strains in well-mixed culture resulting from the fact that rare strategi
118 that monochloramine cometabolism occurred in mixed cultures similar to those found in drinking water
125 munities, study of individual organisms in a mixed culture using existing flux analysis methods is di
126 s were isolated from the PCBs-dechlorinating mixed culture using trichloroethene (TCE) and vinyl chlo
127 nt or depletion of PGK1 point mutants from a mixed culture was consistent with the expected results b
128 reductive dechlorination by a methanogenic, mixed culture was significantly inhibited when exposed t
129 res, activation of microglia in BDV-infected mixed cultures was associated with a significantly great
130 Moreover, the dominance of nonproducers in mixed cultures was associated with higher resistance to
131 In contrast, in the BDV-infected primary mixed cultures, we observed proliferation of microglia c
135 e Cryptococcus and Trichosporon species, and mixed cultures were often difficult to identify as such.
139 ltures but have a proliferation advantage in mixed cultures, where they can use the IGF-II provided b
140 alococcoides mccartyi strain JNA from the JN mixed culture which was enriched and maintained using th
141 nobacterium Synechocystis sp. PCC 6803) in a mixed culture with heterotrophic bacteria (i.e., Escheri
142 emoving T cells from the mix or treating the mixed culture with immune suppressants enhanced virus pr
143 ring co-culture with P. distasonis or during mixed culture with porcine or bovine faecal microbes pos
144 ell lines and depleted CD56(+) MM cells from mixed cultures with a CD56(-) cell line or adherent bone
145 n of the phrA mutant can also be obtained in mixed cultures with a wild-type strain, suggesting the p
147 atory strains of B. subtilis can co-exist as mixed cultures with group I Bacilli, and that the latter
149 ith sensitive or resistant strains in a well-mixed culture, yet all three phenotypes are recovered in
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