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1 l and MCF10A), colon cancer (HT-29), and normal colon (FHC) cells were incubated with [(14)C]MTHF in culture medium from
4 test the first hypothesis, purified PMNs and cultured HL-60 cells were incubated with [(3)H]-clarithromycin.
6 ected with the adenoviral vector Ad5CMVcatalase and control cells were incubated with Ad5CMVntLacZ for 24 h.
7 Pancreata and primary acinar cells were isolated; acinar cells were incubated with an inhibitor of p110alpha (PIK75) f
12 To probe the extracellular pathway, HepG2/shPCSK9 cells were incubated with conditioned media from transfected
17 Murine splenocytes and bone marrow-derived dendritic cells were incubated with HDEs, and supernatant cytokine conc
18 When Huh7 K2040 and Huh7 L2198S hepatoma cells were incubated with IFN-alpha-2a, expression of ISGs pe
19 pDCs from human peripheral blood mononuclear cells were incubated with infectious or aldrithiol 2 (AT-2)-i
21 haride (LPS) to induce expression of NLRP3, IL1B, and IL18; cells were incubated with LPS and adenosine triphosphate to a
22 ves were tyrosine phosphorylated after wild-type H. ducreyi cells were incubated with macrophages.
29 Primary mouse and human hepatocytes and Huh7 cells were incubated with palmitate, its metabolite lysophosp
30 No cytotoxic effect was observed when bronchial epithelial cells were incubated with PEG-PLGA based formulations.
32 UVA irradiation also induced AKT activation; when cells were incubated with phosphatidylinositol-3-OH kinase/AK
34 To assess Ig agonist activity, PDGFRalpha-expressing cells were incubated with pure Ig and the level of receptor p
35 induction of proliferation; these effects were blocked when cells were incubated with recombinant Bmp2.
36 To determine the effect of IL-12, hPDL cells were incubated with recombinant human IL-12 (p70) in a
39 e at codon 198 showed a significantly higher induction when cells were incubated with selenium and showed a distinct patt
41 In a metabolic cytometry experiment, single cells were incubated with substrate, washed, aspirated into a
42 Primary rat enteric neurons and human SH-SY5Y cells were incubated with supernatants from the mucosal biops
43 ed receptor expression was due to attenuated calcium entry, cells were incubated with the calcium chelator BAPTA-AM (1,2-
44 exed with copper, and nuclear fluorescence was reduced when cells were incubated with the CuDox complex as compared with
45 Prostate cancer, lymphoma, and leukemic cells were incubated with the drug for 4, 16, or 24 hours.
47 man peripheral blood mononuclear cells or mouse bone marrow cells were incubated with Toll-like receptor (TLR) agonists a
50 own-regulation of intracellular legumain activity than when cells were incubated with wild-type cystatin C.
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