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6 To assay changes in the actin cytoskeleton, TM-1 cells were incubated for 24 hours with or without the HepII domain,
7 FG human pancreatic adenocarcinoma cells were incubated for various time periods in media at a physiol
10 ated for a longer period of time to allow maturation, cells were incubated for 8 days in LD followed by 2 days in DD.
13 ations, the class 2 phenotype could be corrected when cells were incubated for 24 hours at reduced temperature (27 degree
19 murine splenocytes and from blood samples of healthy donors were incubated for 8 days under Th2-like conditions with aque
20 e samples (undiluted) spiked with E. coli or N. gonorrhoeae were incubated for 5 min with 1% Tween 80.
23 Unfractionated BMDSC from diabetic Lepr mice were incubated for 20 hours with SDF-1alpha (100 ng/mL) or bo
24 ary cultures of neurons and glial cells from Npc1(-/-) mice were incubated for 24 h with 0.1 to 10 mm CD after which surv
26 For ex vivo studies, SVG segments from 24 patients were incubated for 6 hours with atorvastatin 0, 5, or 50 mumo
30 Hepatocytes isolated from adult male Sprague-Dawley rats were incubated for 4 hours in buffer containing the hydrophob
32 extensor digitorum longus muscles isolated from normal rats were incubated for 1 hr in the Krebs-Henseleit buffer media c
33 extensor digitorum longus muscles isolated from normal rats were incubated for 1 hr in the Krebs-Henseleit buffer media c
34 Human CBSM cells isolated from donor corneoscleral rims were incubated for 24 hours with control (0.015% ethanol in D
35 Nearly 90% of the ovules aborted when roots were incubated for 12 h in a hydroponic medium supplemented w
40 After seeding at 15 x 10(6) cells/cm2, scaffolds were incubated for 10 days in a roller bottle with or without
41 After seeding at 2 x 10(6) cells/cm2, scaffolds were incubated for 5 days in a roller bottle, with or without
43 In the ex vivo model, posterior segments were incubated for up to 120 minutes in peptide solution.
44 broblasts attached to collagen-glycosaminoglycan substrates were incubated for 5 wk in media containing 0.0 mM or 0.1 mM
45 ls isolated from lung samples incidental to patient surgery were incubated for 24 h (overnight) in medium (control) or 1
47 h muscle strips by reversible permeabilization, and tissues were incubated for 2 days to allow for protein expression.
48 oduced into tracheal smooth muscle tissues, and the tissues were incubated for 2 days to allow for protein expression.
50 For the in vitro wound assay, triplicate wells were incubated for 1, 3, 5, and 7 days using 0.1% fetal bovin
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