コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
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 the robust methylation efficiencies in this mixed culture.
5 ive bacteria from killing by phage lambda in mixed culture.
6 argoes to distinct cell populations within a mixed culture.
7 ination of cancer cells from healthy ones in mixed culture.
8 smission or new infection events in cells in mixed culture.
9 mccartyi biomarkers in a well-characterized mixed culture.
10 stradiol (EE(2)) under aerobic conditions in mixed culture.
11 ncreasing the proportion of swarmer cells in mixed culture.
12 that inhibits growth of Escherichia coli in mixed culture.
13 xed culture requires its separation from the mixed culture.
14 metabolic fluxes of targeted organisms in a mixed culture.
15 antify the frequencies of pairs of clones in mixed culture.
16 predict growth and infer relative fitness in mixed cultures.
17 ation for 400 single-pathogen cultures and 9 mixed cultures.
18 sing the same stimuli that were effective in mixed cultures.
19 t gram-negative bacteria in 12 of 41 (29.3%) mixed cultures.
20 isms and to isolate individual colonies from mixed cultures.
21 signal that mediates appropriate matching in mixed cultures.
22 hibited a modest replication disadvantage in mixed cultures.
23 d and easy to interpret and may be used with mixed cultures.
24 olony is possible, allowing the screening of mixed cultures.
25 competitive success over other organisms in mixed cultures.
26 being more resilient and dominating in well-mixed cultures.
27 ory setting when microorganisms are grown as mixed cultures.
28 use of technical difficulties in maintaining mixed cultures.
29 om both pure isolates and samples containing mixed cultures.
30 ns, which is in line with data obtained from mixed cultures.
31 with conventional bulk measurements of EBPR mixed cultures.
32 hurdle for isotopomer-based flux analysis of mixed cultures.
33 ion induces loss of self-renewing cells from mixed cultures.
34 distribution of PHA storage activity in this mixed culture activated sludge microbial communities.
38 r, inhibition of astrocytic NFAT activity in mixed cultures ameliorated Abeta-dependent elevations in
39 obial biology arose in the context of a very mixed culture and cannot be understood without unscrambl
40 col that can discriminate between strains in mixed culture and quantify their relative abundances.
41 ion for these microbes, even when growing in mixed culture and utilizing a shared substrate which has
43 edator-prey, Stylonychia pustula-P. caudatum mixed culture, and cheese microbial systems revealed con
44 how that individual species or serovars in a mixed culture are identifiable among a biological VOC ba
55 ta indicate that nearly all neurons in these mixed cultures can undergo apoptosis in response to appr
57 ins can be individually purified from such a mixed culture (cocultivation) through the use of a combi
60 The mice were injected subcutaneously with mixed cultures containing Escherichia coli, Bacteroides
61 V-JHM, and MHV-A59/MHV-JHM) were passaged in mixed cultures containing progressively increasing conce
64 of inorganic N availability, ECM species in mixed cultures demonstrated a preference for C over N, i
68 distributed relative to themselves, but, in mixed culture, each predator clusters around its respect
71 e in suppressing E. coli in these planktonic mixed cultures, even though PEf1 reached higher concentr
72 her reports of cooperative invasion in which mixed cultures exhibit a follow-the-leader mechanism, we
76 such as acetate are easily produced through mixed culture fermentation of many biological waste stre
77 uction of fine chemicals following undefined mixed culture fermentation, embedding carbon in industri
80 mposer and biosurfactant producer in pure or mixed cultures for the bioremediation of diesel-contamin
81 olation of Candida species either in pure or mixed culture from intraoperatively collected abdominal
84 mpeted by B. animalis subsp. lactis Bl-04 in mixed cultures growing on raffinose, the preferred ligan
85 ed monochloramine cometabolism by nitrifying mixed cultures grown under more relevant drinking water
88 e, studies of bacterial pathogenesis in well-mixed cultures have revealed virulence factors and the r
91 the responses of fresh control CD4+ cells in mixed cultures indicating that the apparent "anergy" was
92 uppress the response of naive CD4 T cells in mixed cultures, indicating that this tolerance mechanism
94 le this 'gene-sharing' cannot evolve in well-mixed cultures, it does evolve in a spatial population l
95 nin, on which astrocytes overgrow neurons in mixed cultures, laminin-coated soft gels encourage attac
98 a series of continuously fed dechlorinating mixed-culture microcosm experiments (n = 26), we varied
99 wever, when grown in MOPS minimal medium, in mixed cultures, more hmp mutant cells were recovered tha
100 nown target and two hypersensitive loci in a mixed culture of 233 strains in the presence of the drug
102 this inflammatory neurodegeneration using a mixed culture of neurons, microglia, and astrocytes, eit
104 s using an anaerobic bioreactor containing a mixed culture of sulfate-reducing bacteria which precipi
105 d DA cell death in mesencephalic neuron-glia mixed culture of wild-type (WT) mice, but this was atten
109 y from inoculated medium, sterile swabs, and mixed cultures of C. jejuni and coliform bacteria were t
110 This capability plus the ability to detect mixed cultures of Candida spp. promises to improve and s
111 n of Th1 and Th2 cytokines in OVA-stimulated mixed cultures of CD4(+) T cells from Tpl2(+/+)/OT2 or T
115 s of neurodegeneration/neuroprotection using mixed cultures of cortical cells challenged with beta-am
116 ection against excitotoxic neuronal death in mixed cultures of cortical cells; and 3) protection agai
118 f isolated crest-derived cells but did so in mixed cultures of crest- and non-neural crest-derived ce
120 y to show that TGFbeta promotes migration in mixed cultures of embryonic sclerotome and associated me
121 ces these cells to differentiate and produce mixed cultures of epithelial and mesenchymal cells.
122 a shift in excitation/inhibition balance in mixed cultures of hippocampal neurons exposed to SAVAs.
125 have benchmarked our approach using pure and mixed cultures of neuroblastoma and astrocytoma cell lin
126 but unlike GLT-1, the addition of dbcAMP to mixed cultures of neurons and astrocytes caused GLAST pr
127 GLT-1 protein, but the addition of dbcAMP to mixed cultures of neurons and astrocytes did not cause G
133 of this work was to evaluate how the use of mixed cultures of Saccharomyces cerevisiae and Lachancea
141 bolic flux analysis of a given organism in a mixed culture requires its separation from the mixed cul
142 coexistence between the two strains in well-mixed culture resulting from the fact that rare strategi
146 that monochloramine cometabolism occurred in mixed cultures similar to those found in drinking water
147 actate platform demonstrates the benefits of mixed cultures, such as their modularity and their abili
154 munities, study of individual organisms in a mixed culture using existing flux analysis methods is di
155 s were isolated from the PCBs-dechlorinating mixed culture using trichloroethene (TCE) and vinyl chlo
156 ting density-dependent microbial growth in a mixed culture utilizing data from monoculture and mixed-
157 nt or depletion of PGK1 point mutants from a mixed culture was consistent with the expected results b
158 reductive dechlorination by a methanogenic, mixed culture was significantly inhibited when exposed t
159 res, activation of microglia in BDV-infected mixed cultures was associated with a significantly great
160 Moreover, the dominance of nonproducers in mixed cultures was associated with higher resistance to
161 In contrast, in the BDV-infected primary mixed cultures, we observed proliferation of microglia c
165 e Cryptococcus and Trichosporon species, and mixed cultures were often difficult to identify as such.
166 all Lambda(C/Cl) could even be reversed when mixed cultures were precultivated on VC or DCEs and subs
170 ltures but have a proliferation advantage in mixed cultures, where they can use the IGF-II provided b
171 alococcoides mccartyi strain JNA from the JN mixed culture which was enriched and maintained using th
172 . coli expressing arsI, arsH or arsP grow in mixed culture with Burkholderia sp. MR1 in the presence
173 nobacterium Synechocystis sp. PCC 6803) in a mixed culture with heterotrophic bacteria (i.e., Escheri
174 emoving T cells from the mix or treating the mixed culture with immune suppressants enhanced virus pr
175 ring co-culture with P. distasonis or during mixed culture with porcine or bovine faecal microbes pos
176 ell lines and depleted CD56(+) MM cells from mixed cultures with a CD56(-) cell line or adherent bone
177 n of the phrA mutant can also be obtained in mixed cultures with a wild-type strain, suggesting the p
179 atory strains of B. subtilis can co-exist as mixed cultures with group I Bacilli, and that the latter
183 ith sensitive or resistant strains in a well-mixed culture, yet all three phenotypes are recovered in