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1 Further discs were alumina-air-abraded.
2 Two hundred forty porcelain discs were air-abraded.
3 LR3(-/-), TRIF(-/-), and MyD88(-/-) mice was abraded and stimulated with the synthetic TLR3 ligand po
5 LR2(-/-), TLR9(-/-), and MyD88(-/-) mice was abraded and treated with Pam(3)Cys, LPS, or CpG DNA, whi
7 helium of C57BL/6 and gene knockout mice was abraded, and 1 x 10(7) S. marcescens were added in the p
8 ium of BALB/c, C3H/HeJ, and C3H/HeN mice was abraded, and Pseudomonas aeruginosa endotoxin (10 microg
12 fected PA-III cells were inoculated over the abraded calvaria of nude mice, large tumors formed with
14 and a 2-mm diameter punch was placed on the abraded corneal epithelium of either untreated or cyclop
16 Using a murine model of keratitis in which abraded corneas are infected with P. aeruginosa parent a
21 ined decussating enamel rods but was rapidly abraded following weaning, despite the mice being mainta
24 find significant performance enhancements in abraded heterostructures compared to those fabricated th
27 n of aged dust particles relative to freshly abraded, metallic particles from the wheel/track/brake s
29 spores or vegetative bacilli onto intact or abraded mouse flank skin, followed by evaluation of the
33 ealed that in the respirable fraction of the abraded particles, approximately 4000 ppm of the MWCNTs
43 ndomly assigned to 3 groups: C, control (air abraded); SG, sol-gel silica infiltration; and GI, glass
44 layers of approximately 10 microns each were abraded simultaneously with reference slabs of sound ena
45 cur following topical administration through abraded skin and requires phosphatidylserine receptor, A
47 mas as early as 3 weeks after application to abraded skin on the muzzles and tails of athymic NCr nud
48 1 X 10(7) B. anthracis (Sterne) spores onto abraded skin or injected with the spores intradermally o
50 EBOV GP was applied to the surface of gently abraded skin to remove the stratum corneum; epidermal ke
51 curs through contact of mucous membranes and abraded skin with freshwater contaminated by pathogenic
57 amont oats were dehulled and/or sequentially abraded to produce ten pearling fines and corresponding
59 R4(-/-), TLR9(-/-), and MyD88(-/-) mice were abraded using a trephine and epithelial brush and were e
60 lock textile swatches made of polyester were abraded using abrasion tests with a Martindale tester.