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1 uman lung epithelial cells to the carcinogen crocidolite.
2 increased with increasing treatment dose of crocidolite.
3 ocation, were induced by both chrysotile and crocidolite.
4 se dependent for all types of asbestos, with crocidolite (5 microg/cm2) inducing 15.0+/-1.1% (mean+/-
6 (rabbit or human) were exposed to asbestos (crocidolite, amosite, or chrysotile) or control particle
7 ing the similarities and differences between crocidolite and chrysotile asbestos in terms of their tr
11 d that incubation with low concentrations of crocidolite asbestos (0.5-1.25 microg/cm(2)) resulted in
13 (MET5A) exposed to various concentrations of crocidolite asbestos and man-made vitreous fibers (MMVF-
16 e, to focus on a specific membrane effect of crocidolite asbestos exposure, which deserves to be test
19 57/BL6 mice were exposed to 7-mg/m(3) air of crocidolite asbestos for 5 and 30 days, the times requir
20 te asbestos was addressed by instillation of crocidolite asbestos in a series of wild-type or SPARC-n
21 ew of the transcriptional changes induced by crocidolite asbestos in A549 human lung epithelial cells
24 enitor cells of lung cancers, we report that crocidolite asbestos initially depletes intracellular gl
26 terations in gene expression associated with crocidolite asbestos or cristobalite silica exposures in
27 ells to nitric oxide (NO) in the presence of crocidolite asbestos resulted in a marked decrease in in
29 ole of SPARC in the in vivo lung response to crocidolite asbestos was addressed by instillation of cr
30 Activation of activator protein (AP-1) by crocidolite asbestos was examined in vitro in a JB6 P+ c
31 esothelial (RPM) cells, RPM cells exposed to crocidolite asbestos, and rat mesotheliomas, subsets of
32 cell signaling, we evaluated the effects of crocidolite asbestos, EGF and H2O2, on MAPK activation i
35 que to alpha-quartz, being also increased by crocidolite asbestus fibers but not by titanium dioxide
37 ssively increased for 10 or more weeks after crocidolite exposure, but returned to background levels
40 human-hamster hybrid (A(L)) cells induced by crocidolite fibers in an attempt to determine the role o
41 dy specific for 8-OHdG, we demonstrated that crocidolite fibers induced a dose-dependent increase in
42 CD59 locus induced by a 4 microg/cm2 dose of crocidolite fibers was increased by more than 3-fold (P
44 minerals-grunerite (amosite) and riebeckite (crocidolite)-have been almost completely eliminated from
46 analyses was used to explore the effects of crocidolite in the context of known molecular interactio
47 G12 cells were treated with 3 microg/cm2 of crocidolite in the presence of nitric oxide-generating c
49 bust, comprehensive data set documenting the crocidolite-induced changes in the A549 transcriptome wa
52 Methods: Subjects were from two cohorts: 1) crocidolite mine and mill workers and Wittenoom Township
54 h inhibits membrane actin repair mechanisms, crocidolite or applied Fe(3+)/H(2)O(2) invariably produc
57 ed for the identification of novel, putative crocidolite-related genes, leading to several new hypoth
58 tion paints a much broader landscape for the crocidolite response than was previously appreciated and
59 lectrophysiological modifications induced by crocidolite suggested a modification of an intrinsic chl