1 We exposed 17 patients with SCD and 16 control participants t
2 We exposed 5XFAD mice and littermate controls to dim-light vs
3 To develop a neurological model for NiV infection,
we exposed 6 adult African green monkeys to a large-particle
4 and multiple cognitive domains in a non-aversive way, here
we exposed 6-month-old C57BL/6J male mice to whole-body space
5 We exposed a human trophoblast line, HTR8/SVneo, to PFBS.
6 We exposed a temperate heath/grassland to eCO(2) , warming, a
7 We exposed acoustically naive juvenile male and female cowbir
8 To test this hypothesis,
we exposed adult female Long-Evans rats to 2 weeks of moderat
9 To better understand these effects,
we exposed Arabidopsis plants at the seed setting stage to a
10 Here,
we exposed Atlantic haddock embryos to 10 and 80 mug oil/L (0
11 In this study,
we exposed autoimmune-prone female MRL/lpr mice to a human-re
12 We exposed calling males to predator cues under three differe
13 We exposed cells to mechanical, genetic, and pharmacological
14 Accordingly,
we exposed chimeric (CD45.2/CD45.1) mice to concentrated PM(2
15 Here,
we exposed Escherichia coli to a range of indole concentratio
16 In this study,
we exposed female FVB mice to weekly alternating light-dark c
17 We exposed field colonized benthic communities to aqueous met
18 n a large-scale field experiment conducted over five years,
we exposed &
gt; 106 000 transplants to historical, current, or f
19 We exposed hairless mice to low-dose UV radiation over a peri
20 We exposed healthy men and women to a stress (n = 27) or cont
21 We exposed human participants (male and female) to auditory c
22 We exposed human participants to auditory cues that predicted
23 We exposed human primary endothelial cells to radiation as a
24 In vitro,
we exposed human primary monocytes to (nor)adrenaline for 24
25 To investigate this possibility,
we exposed inland silversides (Menidia beryllina) to environm
26 We exposed lab raised beagles to varying densities of uninfec
27 We exposed male and female mice to morphine for one week, wit
28 We exposed male and female mice to physiologically comparable
29 We exposed male fish to sublethal low-dose ionizing radiation
30 To address this issue,
we exposed mice to a single episode of voluntary exercise, an
31 entral role of the liver in peripheral glucose homeostasis,
we exposed mice to filtered air or PM(2.5) for 16 weeks and e
32 We exposed mice to secondhand smoke for 8 wk, followed by a p
33 To address these issues,
we exposed Moina dubia to lead (Pb, 50 mug/L) under two tempe
34 In this study,
we exposed monarch larvae to six pesticides (insecticide: clo
35 We exposed mothers, fathers or both parents to visual cues of
36 Using mesocosms
we exposed phytoplankton to ambient (390 muatm) or future CO(
37 When
we exposed populations of Drosophila melanogaster to intense
38 In common-garden experiments,
we exposed populations of two desert rodents to two different
39 er understand the DNA damage response (DDR) in these cells,
we exposed pregnant mice to ionizing radiation (IR) at specif
40 We exposed preneoplastic, hTERT-immortalized Barrett's cell,
41 We exposed primary cells to disease-related modifiers that al
42 nt to proteotoxic stress elicited by brefeldin A treatment,
we exposed primary neurons to three different Parkinson's dis
43 roplastics at unrealistic environmental concentrations here
we exposed Salpa fusiformis to fractured and UV exposed polye
44 To this end,
we exposed sheepshead minnows (Cyprinodon variegatus) at thre
45 Using a repeated measures design,
we exposed small colonies of introduced O. taurus and native
46 We exposed successive generations of the wasp Nasonia vitripe
47 In this study,
we exposed the CBB panel of seven bacterial strains (nitrifyi
48 In this study,
we exposed Varroa mites to DWV type A via feeding on artifici
49 In the current study,
we exposed wild-caught zebrafish to oxazepam (~7 mug L(-1)) f
50 Here,
we exposed wild-type male mice to 5-60 min of 40 Hz or contro