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1 e + fluoxetine (20 mg/kg/day in saline; oral gavage).
2 t (3 mg/kg rosiglitazone or vehicle via oral gavage).
3 n fungicide and donor cecum content via oral gavage.
4 en 10(8) bacteria for 15 consecutive days by gavage.
5 with wild-type or mutant Salmonella by oral gavage.
6 entrations doubled following DHA but not Asc gavage.
7 tinal NV, as did GW0742 administered by oral gavage.
8 n jejunal loops and in mice following apelin gavage.
9 ere collected after 30, 120 and 180 min post-gavage.
10 cal microbiome 24 h after a single probiotic gavage.
11 ine, was discovered in mice after alpha-CEHC gavage.
12 and on Day 21, mice received ethanol by oral gavage.
13 n a single dose of TCPOBOP (3 mg/kg) by oral gavage.
14 r a single dose of TCPOBOP (3 mg/kg) by oral gavage.
15 tor poloxamer 407 alone or before oral lipid gavage.
16 ns retinoic acid (atRA), or UDCA and atRA by gavage.
17 Mice were acutely given ethanol by gavage.
18 U/L aspartate aminotransferase 9 hours after gavage.
19 type Cyp c 1 or carp extract by intragastric gavage.
20 n via multiple dosing routes, including oral gavage.
21 bate 80; Control, n = 6) for 12 days by oral gavage.
22 y) or the same volume of the vehicle by oral gavage.
23 mates were infected with C rodentium by oral gavage.
24 ric isomer, 9-cis-retinal, delivered by oral gavage.
25 ter the surgery, the rats received (51)Cr by gavage.
26 tered by implanted capsules or by daily oral gavage.
27 given the synthetic LXR agonist T0901317 by gavage.
28 ide and UMP (a uridine source) and/or DHA by gavage.
29 , whereas the other half received vehicle by gavage.
30 ngle dose of ethanol (6 g/kg body weight) by gavage.
31 arance of lipids from serum after oral lipid gavage.
32 Drugs were administered by oral gavage.
33 strains hyperabsorbed (59)Fe administered by gavage.
34 y) or the same volume of the vehicle by oral gavage.
35 ose with 0.2% Tween 20) via gastrointestinal gavage.
36 Compounds were given once daily by oral gavage.
37 C57BL/6 mice were made cirrhotic using CCl4 gavage.
38 ient diet-fed mice were administered BBR via gavage.
39 fter 4 extra weeks (16 vs. 12 weeks) of CCl4 gavage.
40 and then inoculated them with C. albicans by gavage.
41 and SRP + vitamins K2 and D3 groups by oral gavage.
42 ulin secretion was reduced following glucose gavage.
43 imvastatin was given to some of the rats via gavage.
44 gle dose of ethanol (5 g/kg body weight) via gavage.
45 x2a act differently when delivered orally by gavage.
46 with siCD98 or scrambled siRNA (control) via gavage.
47 later, LL-IL-27 was administered to mice via gavage.
48 g/kg) every 6 h for 3-5 consecutive days via gavage.
49 ogs following repeat oral administrations by gavage.
50 ol in which rosiglitazone was given by daily gavage (10 micromol/kg body wt) immediately after STZ in
53 ded into 7 groups (n=7) and received by oral gavage 30% glucose plus 0.55 g/kg body mass of the follo
55 pG DNA administered to BALB/c mice orally by gavage 48 h or 7 days before oral challenge with virulen
56 ministered orally (25 mg/kg, once a day), by gavage, 7 days before, and 7 days after the AF64A inject
57 inoculated into BALB/c mice by intragastric gavage, 7 of 14 type C isolates were lethal, whereas whe
62 gned two experimental approaches: 1) glucose gavage and 2) hyperinsulinemic intravenous infusion, for
63 were administered C. rodentium by orogastric gavage and analyzed at multiple time points up to post-i
64 fluorescently-labeled ricin to mice by oral gavage and followed transit of the toxin from the gastro
67 small intestine and is induced by olive oil gavage and that the Noc(-/-) mice have reduced chylomicr
68 F1] mice were infected with H. felis by oral gavage and were assessed histologically and serologicall
72 d with carcinine (intravitreal injection and gavage) and exposed to bright light to induce oxidative
73 pared the effects of passively administered (gavaged) and self-administered (two-bottle choice) EtOH.
74 ) rats with ligature + placebo (saline; oral gavage); and 3) rats with ligature + fluoxetine (20 mg/k
75 of human breast milk and infant formulas, by gavage, and plasma samples and brains were collected for
76 /6 mice were fed ovalbumin (OVA) by means of gavage, and subsequent response to immunization with OVA
78 kg/day (0.2 ml) PC-SPES via gastrointestinal gavage; and a control group (n = 10) received 0.2 ml of
80 us BaP (2 micromol each) was administered by gavage as eight weekly doses, whereas I3C (112 micromol/
81 mice where animals were fed with GSE by oral gavage at 200 mg/kg body weight dose during 4 to 28 week
86 AG3340 and DPC-A37668 administered by oral gavage at doses of 3, 10, or 30 mg/mL provided up to 42%
89 of tumor volume on day 17 when delivered by gavage compared with untreated animals (P <or= 0.01), wi
91 deficient mice bearing U87MG xenografts were gavaged daily over 72 hours with 72 or 95 mg/kg of dasat
93 ngs in vivo, Zucker diabetic fatty rats were gavaged daily with water (placebo) or MnCl2 (16 mg/kg of
98 ated with virulent HRV (oral, intranasal, or gavage) developed diarrhea, shed virus nasally and recta
101 129sv mice (12 weeks old) received a single gavage dose of 50 mg/kg BaP at either noon or midnight,
102 amin A content or administering them an oral gavage dose of [(3)H]retinol with or without P-407 treat
103 atal day (PND) 10 were administered a single gavage dose of alpha-, gamma-, or CM-HBCD at 3, 10, and
104 ried out two rounds of experiments with oral gavage doses selected in accordance with no observed adv
105 lnaltrexone (100 mg/kg) were administered by gavage either before or after the surgery, with or witho
107 ral source, broccoli sprout extract (BSE) by gavage every other day for 3 months, with four groups: v
108 rmore, LAL-deficient mice challenged with RE gavage exhibited largely reduced post-prandial circulati
110 s, FcRn(+/-) or FcRn(-/-) neonatal mice were gavage fed TNP-specific IgE as IgG(1) anti-IgE/IgE immun
114 uction of AP-1 activity in the skin, whereas gavage feeding with TPA caused a 34.2-fold induction of
115 njury was induced in newborn rats by hypoxia/gavage feedings, and restitution was determined by asses
121 rafts, administration of anastrozole by p.o. gavage for 21 days elicited pronounced inhibition of tum
122 nylamino) phenylacetic acid (23CPPA) by oral gavage for 26 weeks, was analyzed by immunoassay for pig
123 tion, and another given doxycycline via oral gavage for 28 days beginning on the day of implantation.
124 d 1.0 mg/kg/day LAAM or water via daily oral gavage for 28 days prior to breeding, during breeding, a
126 Gerbils were treated with yokukasan by oral gavage for 30 days, once per day, until the day before i
132 docosahexaenoic acid (DHA; 300 mg/kg/day) by gavage, for 4 wk, and then throughout the subsequent per
134 .05 (high) mug Aroclor 1254/g-body weight by gavage from 1 through 18 days posthatch and later expose
137 ceived simvastatin (2 mg x kg(-1) x d(-1) by gavage) from week 11, there was 100% survival and revers
141 ydroxyethyl)-rapamycin (RAD, 2.5 mg/kg/d, by gavage): Group PMR(5-35) from Day 5 to Day 35, Group PMR
142 a TG excursions in db/db mice after corn-oil gavage (iAUC, 1,500 +/- 470 mg/dL.h for NT ASO versus 16
147 1 ml of 10mg TQ or 200mg LMN suspension, by gavage in two equal doses (morning and evening) of 0.5 m
148 y, CS-ZN-NIMs encoding GFP delivered by oral gavage in vivo induced the production of anti-GFP IgA an
149 ced by levodopa (5 mg/kg twice daily by oral gavage) in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine
151 palmitic acid via direct infusion or by oral gavage increased the localization of PKC-theta to cell m
152 ngle dose of ethanol (5 g/kg body weight) by gavage, induces significant fatty liver and liver injury
153 ongravid female mice following intragastric (gavage) inoculation, namely, (i) disease severity (measu
155 reatment were assessed from P12 to P16: oral gavage, intraperitoneal injection, or subcutaneous injec
156 us, uptake of (59)Fe administered by gastric gavage, intravenously, or intraperitoneally was signific
158 on, we harvested organs from unlabeled ricin-gavaged mice and assessed them for the presence of ricin
163 iodontal disease in humans, whereas the oral gavage models were not effective at inducing the disease
164 rol (cyclosporine A 10 mg/kg per day by oral gavage, n = 10), and isograft negative control (Lewis-to
165 ironolactone (SP) alone (200 mg/kg per d, by gavage, n = 6); or SP combined with nonspecific triple a
167 ospiraceae and Ruminococcaceae, from vehicle-gavaged NOD donors to microbiota-depleted C57BL/6 recipi
175 jected to microbiota transplantation by oral gavage of cecum content obtained from donor CTRL- or HFD
178 ur studies show for the first time that oral gavage of ethanol decreased the beating frequency of all
180 ability was measured in mice with colitis by gavage of fluorescent dextran and quantification of seru
186 de (MDP) to stimulate NOD2 and given an oral gavage of P. gingivalis displayed a reduction of serum i
202 enografts with riluzole for 18 days via p.o. gavage or i.v. injection leads to inhibition of tumor gr
203 ancreas (collected immediately after glucose gavage or insulin infusion) from controls showed signifi
212 skin extract supplemented in addition to oil gavage resulted in significant decrease in plasma trigly
213 closporine, bolus dosages of cyclosporine by gavage, resulting in strongly varying blood levels of cy
214 btained 1 h after EtOH intoxication (5 g/kg, gavage), revealed decreases in the cell-surface fraction
217 Mice given atorvastatin through gastric gavage showed increased AMPK, acetyl-CoA carboxylase, an
221 e, administered by intravitreal injection or gavage, strongly protected mouse retina against light-in
224 0.1, 1, or 10 mg/kg/day) twice daily by oral gavage; the first dose was given 4 h before inoculation
225 g daily) treatment was administered via oral gavage to 250 g male rats for 10 days before PCO and was
227 95 or vehicle alone was administered by oral gavage to C57BL/6 mice that were challenged with 28 dail
228 lfrogs to equivalent doses of Au NPs by oral gavage to compare the bioavailability of NPs through dir
231 triadimefon, was administered daily via oral gavage to male Sprague-Dawley rats at doses of 300, 300,
233 f 8:2 FTOH or 6:2 diPAP at 100 mg/kg by oral gavage to monitor biotransformation and extent of protei
236 (Pimephales promelas) were exposed by single gavage to SWCNTs and their distribution was tracked usin
242 rough the mouse gastrointestinal tract after gavage was followed in real-time by whole-body imaging.
244 stine mucosa phylloquinone content 4 h after gavage was increased in mice overexpressing SR-BI compar
246 00 mg/kg/day in divided doses by twice-daily gavage), we monitored: 24-h urinary Ca2+ and Mg2+ excret
247 lacking rod phototransduction (n = 110) were gavaged weekly for 6 months with 50 mg/kg QLT091001, eit
249 out spironolactone (Spi, 100 mg/kg per daily gavage) were compared with unoperated/untreated and unin
253 27 male Wistar rats by means of weekly oral gavage with 5 mL of 1.5% DEN solution per kilogram of bo
254 arily for 5 weeks, they were treated by oral gavage with a mixture of environmentally relevant PCB co
255 l diet (RBD) for two weeks, followed by oral gavage with a saturated lactose solution (30 g/kg) in th
259 t formation in bone marrow cell cultures and gavage with BaP stimulated bone resorption and osteoclas
261 g animals were treated daily for 3 d by oral gavage with erlotinib at 50 and 150 mg/kg, CL-387,785 (a
262 monas gingivalis (Pg); 4) group G-PgFn: oral gavage with Fusobacterium nucleatum + Pg; 5) group I-Pg:
264 -2-deficient mice were inoculated by gastric gavage with Helicobacter hepaticus, an enteric bacterial
265 ceptor, and/or TSLP mAbs before initial oral gavage with MCT/EW to suppress FA development; treatment
266 diated FA was induced in BALB/c mice by oral gavage with medium-chain triglycerides (MCTs) plus egg w
268 ase induced by ligature; 3) group G-Pg: oral gavage with Porphyromonas gingivalis (Pg); 4) group G-Pg
269 sealed anus were inoculated by intragastric gavage with type D isolates, 7 of 10 type D isolates wer
272 immunodeficient rodent hosts, and hosts were gavaged with a range of phthalate doses over multiple da
273 Wild-type (B6CBA) and hph-1 mice were orally gavaged with a selective PPARdelta activator, GW501516 (
274 o investigate these mechanisms, rodents were gavaged with Asc or its oxidized form dehydroascorbic ac
286 of intestinal inflammation by LGG, mice were gavaged with LGG containing beads and treated with dextr
290 ty acids were present in the digesta of rats gavaged with raw (448 mg g(-1) digesta dry matter (DDM))
294 exhibit such light-induced retinopathy until gavaged with the artificial chromophore, 9-cis-retinal.
298 over rats were dosed daily for 12 days (oral gavage) with either vehicle (control, 0.5% w/v hydroxypr
299 graft growth in nude mice when given by oral gavage, with no marked alterations in normal tissue hist
300 introduction into the ileum than after oral gavage, with rAd5 showing greater potency than the rAd35
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