1 ce flight simulation studies of 105 and 205 days' duration,
we exposed 10 healthy men to 3 salt intake levels (12, 9, or
2 We exposed 36 specimens of tambaquis to acidic water (pH 4.0)
3 ssful experience during adolescence affects adult behavior,
we exposed adolescent male and female C57BL/6J mice to chroni
4 ffects mitochondrially transcribed mRNA (mtRNA) expression,
we exposed adult male rats to both acute and chronic immobili
5 We exposed Arabidopsis thaliana plants to herbivory and inves
6 To generate cetuximab-resistant cells,
we exposed cetuximab-sensitive colorectal cancer cells to cet
7 To consider multiple metal-metal interactions,
we exposed D. magna neonates to Cd, Cu, Ni, or Zn alone and i
8 Therefore,
we exposed damselfly larvae to chlorpyrifos and cues from pre
9 igate the chronological events of early prion pathogenesis,
we exposed deer to CWD prions and monitored the tissue distri
10 Using a split half-sibling design,
we exposed embryos of 10 families from each of two population
11 Here,
we exposed F2 hybrids, used to separate Eda genotype from gen
12 We exposed five Australian frog species to Bd, and monitored
13 We exposed four common CCA genera and a crustose calcifying r
14 In an effort to fill this gap
we exposed four naive clones of green peach aphid (Myzus pers
15 We exposed fragments of eight Acropora millepora colonies (ge
16 ors, tissue distribution, and metabolite formation in fish,
we exposed gilt-head bream (Sparus aurata) to AMI in seawater
17 As a proof of concept
we exposed growing colonies of Escherichia coli to a virulent
18 rgy metabolism and drug metabolism crosstalk in this study,
we exposed HepG2 cells to varying glucose concentrations.
19 We exposed human bronchial epithelial cultures (HBECs) to air
20 To investigate this,
we exposed human fetal testes (7-17 gestational weeks (GW)) t
21 To test the hypothesis,
we exposed human lung fibroblasts with various doses of nicot
22 Thus,
we exposed intact sediment cores containing European flat oys
23 genesis from those likely to be secondary to hyperglycemia,
we exposed islets from human donors to normal or high glucose
24 We exposed isolated rat islets for 1 h to increasing glucose
25 We exposed juvenile emerald rockcod Trematomus bernacchii to
26 Building on their natural responsiveness to odors,
we exposed juvenile rats for 1 h daily to a dynamic series of
27 We exposed larval mayflies (Baetis tricaudatus) and their foo
28 We exposed larval wood frogs (Lithobates sylvaticus) to one o
29 We exposed male mice implanted with wireless telemetry transm
30 We exposed mice to chronic cocaine or chronic social defeat s
31 asia by stimulating stromal endothelial cell proliferation,
we exposed mice to cigarette smoke for 6 months.
32 increase light exposure without eliminating daily rhythms,
we exposed mice to either a standard photoperiod or a long da
33 We exposed mice with conditional deletion of the Tnfaip3 gene
34 To test this hypothesis,
we exposed model-populations of the shredder Gammarus fossaru
35 Here,
we exposed MPCCs to hypo-, normo- and hyperglycemic culture m
36 We exposed multi-trophic protist microcosm landscapes with on
37 We exposed multiple ramets of 26 goldenrod genets to nutrient
38 We exposed oak (Quercus robur) saplings under wet and dry soi
39 In a third experiment
we exposed only the mother, or only the offspring to the elev
40 We exposed pig and human airway explants, pig and human ASL,
41 Here
we exposed populations of Drosophila melanogaster to repeated
42 We exposed pregnant outbred CD1 female mice and the male prog
43 We exposed purified NK cells and full PBMCs from healthy dono
44 We exposed rats to two different experiences (running in diff
45 We exposed RNA oligomer segments from the genome of bacteriop
46 To address these questions,
we exposed Scnn1b transgenic (Scnn1b-Tg(+)) mice to SHS from
47 We exposed the aquatic larvae to the pesticide esfenvalerate
48 We exposed the P5.5 to -11.5 explants to various concentratio
49 o investigate this knowledge gap in early CWD pathogenesis,
we exposed white-tailed deer to CWD prions by mucosal routes
50 Using controlled laboratory experiments,
we exposed wild-caught amphibian species with terrestrial and