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1               Control rats (n = 21) received sterile water.
2 rface coolant consisting of air (15 psi) and sterile water.
3 um into a 35-cc syringe preloaded with 28 mL sterile water.
4  subjects were injected with 5.0 microliters sterile water.
5 quot of freshly reconstituted Abeta(1-42) in sterile water (100 microM, pH 3.6) did not effectively s
6 eceive 0.5 mL 24% sucrose solution or 0.5 mL sterile water 2 min before undergoing a clinically requi
7  compared to fresh frozen plasma (28.6%) and sterile water (20.0%) (P = 0.01).
8 aration for PCR included mixing the stool in sterile water and extraction of nucleic acid using the M
9  1, lyophilised BPZE1 was reconstituted with sterile water and given intranasally (0.4 mL delivered t
10  nanoparticles (SPIONs) was verified in both sterile water and human serum at room temperature 6 and
11                                In tests with sterile water and sterile medium, the device maintained
12 he latter served as a positive control, with sterile water as a negative control.
13 f AGS-v with adjuvant (Montanide ISA 51), or sterile water as placebo.
14 perature and reconstituted within minutes in sterile water but are probably the least explored altern
15  doped PpyNWs was lifted on a single drop of sterile water by surface tension, and deposited onto a s
16 naltrexone (NTX), or an equivalent volume of sterile water (CO) and sacrificed 4 h later (i.e. 16:00
17 iferation of both cell lines by up to 40% of sterile water controls.
18  was dunked in sputum, swirled in 700 muL of sterile water (dunk and swirl method) and tested by the
19                                              Sterile water flushed through the units onto heterotroph
20 n intensified disinfection protocol and used sterile water for heater-cooler units of cardiopulmonary
21 ference was recorded between the sucrose and sterile water groups in the magnitude or latency of the
22 rrect lever response perseverations than did sterile water-injected subjects.
23 in infants given sucrose than in those given sterile water (mean 5.8, 95% CI 3.7-7.8 vs 8.5, 7.3-9.8;
24 water (sucrose: mean 0.10, 95% CI 0.04-0.16; sterile water: mean 0.08, 0.04-0.12; p=0.46).
25 ome (n = 11) after instillation of 60 microL sterile water onto the ocular surface.
26 rated by a 10-min infusion of 5% dextrose in sterile water, or three successive 10-min IV infusions o
27 tion interval and a 5-mL interacquisition of sterile water produced good images of the simulated fall
28 asonic scalers not equipped with a dedicated sterile water reservoir.
29   No treatment, or intravitreal injection of sterile water, resulted in an approximately 50% loss of
30 lidomide dissolved in dimethyl sulfoxide and sterile water, starting at a tumor diameter of 0.7 cm+/-
31  who received sucrose and those who received sterile water (sucrose: mean 0.10, 95% CI 0.04-0.16; ste
32 red from thiopental sodium powder mixed with sterile water to create a concentration of 100 mg/mL.
33            In an animal study, ampicillin or sterile water was administered orogastrically in serotyp
34 control wild-type oocytes microinjected with sterile water was inhibited essentially 100% by Tg.
35 d intratracheal aerosolized LPS (5 mg/kg) or sterile water with concurrent intravenous injection of O