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1 , mice were given saline or ethanol (5 g/kg, intragastrically).
2 t a dose of 50 mg/kg (5 x 10(9) CFU/kg) (g) (intragastrically).
3 allowed to self-administer ethanol or water intragastrically.
4 hen administered either intraperitoneally or intragastrically.
5 t is hypervirulent in mice when administered intragastrically.
6 n live S. sanguis, CB11, or type II collagen intragastrically.
7 nol (5 g/kg body weight) once every 24 hours intragastrically.
8 ze the gastrointestinal tract when delivered intragastrically.
9 nimals fed the TPN solution intravenously or intragastrically.
10 Either PHT or sham-operated rats received intragastrically 100% ethanol, and the stomachs were exc
11 intraperitoneally and the 197 mutants tested intragastrically, 12 mutants with 50% lethal doses great
13 osed to either water or ethanol (0 or 4 g/kg intragastrically, 3 days on, 2 days off, ~P30-P50, 4 cyc
14 e mice were administered high levels of DMBA intragastrically, 70% developed highly malignant lymphom
17 llected over a 2-hour period after rats were intragastrically administered Indo (25 mg/kg) or an equi
18 e-1, and cyclooxygenase-2 knockout mice were intragastrically administered saline, 0.6N HCl, or aspir
19 omeprazole, ranitidine, or cimetidine, were intragastrically administered saline, aspirin, or indome
20 A pool of wild-type TUCH was prepared and intragastrically administered to eight cesarean section-
23 10 ZD rats were treated with zinc gluconate intragastrically and switched to ZS diet; the remaining
24 g were exposed to HDM intranasally or peanut intragastrically, and immune inflammatory and physiologi
25 Rats were given ethanol (4 g/kg body wt) intragastrically, and Kupffer cells were isolated 0-48 h
27 ting reflex) in rats that were given ethanol intragastrically but not in those given ethanol intraper
30 red s.c., i.p., perorally, intranasally, and intragastrically, demonstrating that attenuated CMV appl
31 BCP, when administered intraperitoneally or intragastrically, dose-dependently attenuated cocaine se
35 peptidase activities in cytosol samples from intragastrically ethanol-fed rats were not restored to c
38 rats received 1 ml of 50% E or 1% A solution intragastrically for 1 min during in situ gastric lumina
42 tion (TPN) solutions either intravenously or intragastrically had small intestinal gut-associated lym
43 enase inhibitor, meclofenamic acid (5 mg/kg, intragastrically), had no effect on either parameter.
48 .75 mL HCl (0.05-0.3 N) or saline were given intragastrically in controls and animals after vagotomy,
49 e isolated from Peyer's patch tissue of mice intragastrically infected and treated with chloramphenic
51 gB and DeltaP4inlA strains was attenuated in intragastrically inoculated guinea pigs, with the Deltas
52 increased the severity of infection in mice intragastrically inoculated with Listeria monocytogenes.
53 ect of captopril or losartan (100 or 5 mg/kg intragastrically, respectively) was compared with that o
54 pranlukast (ONO-1078, SB 205312) (20 mg/kg, intragastrically), significantly inhibited both the bron
56 e or after peanut ingestion was administered intragastrically to BALB/c mice at different ages, and m
57 ying effector domain content were inoculated intragastrically to mice, and the time to death was moni
60 anufacturing Practice product of WRSd1 given intragastrically to rhesus monkeys proved safe and immun
63 Ab RB6-8C5-treated mice died when inoculated intragastrically with as few as 4 x 10(4) L. monocytogen
65 Rats with esophageal ulcers were treated intragastrically with either celecoxib (10 mg/kg, once d
66 onkeys (Aotus nancymae) each were inoculated intragastrically with increasing doses of Campylobacter
69 dels, H. pylori-free animals were inoculated intragastrically with mixtures of H. pylori strains, bac
73 stologically in 82 of 122 piglets inoculated intragastrically with Shiga-toxigenic Escherichia coli b
74 e expressing a transgenic TCR were immunized intragastrically with the cognate Ag to elicit a vigorou