ライフサイエンスコーパス: orogastric

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1 al model of lipid peroxidation consisting of orogastric administration of CCl4 to rats was used.

2 Orogastric administration of fatty acids elevated blood

3 Orogastric administration of virstatin protects infant m

4 the effect of DeltatoxRS in vivo using a new orogastric adult murine model of colonization.

5 To our knowledge, the orogastric adult murine model reported here is the first

6 B cells and antibodies, were as resistant to orogastric and disseminated candidiasis of endogenous or

7 the IL-1 receptor were highly susceptible to orogastric but not intraperitoneal infection with Salmon

8 Although highly susceptible to orogastric candidiasis, T-cell receptor delta- and alpha

9 r IL-4 deficiency enhanced susceptibility to orogastric candidiasis.

10 KO, and wild-type (immunocompetent) mice to orogastric candidiasis.

11 enuated LT adjuvant (LTK63) by intranasal or orogastric delivery, induced high antigen-specific serum

12 (GC-C-/-) were administered C. rodentium by orogastric gavage and analyzed at multiple time points u

13 technique, during which mice received daily orogastric gavage with either UDCA or vehicle only.

14 ium and perish shortly after epicutaneous or orogastric infection respectively.

15 d that neonatal mice are highly resistant to orogastric infection with Yersinia enterocolitica.

16 the alimentary tract, and reduced numbers of orogastric infections demonstrated not only that probiot

17 Rats were given an orogastric infusion (0.25 ml) of either AF or 0.9% salin

18 0.0, 0.01, or 0.03 microg, in saline) and an orogastric infusion of 0.25 ml amniotic fluid or saline

19 ctamase were administered 24 and 12 h before orogastric inoculation of piperacillin-resistant pathoge

20 taeae(860-939) as a vaccine was evaluated by orogastric inoculation of rabbits with RDEC-1Deltaeae(86

21 After orogastric inoculation of VRE, clindamycin-treated mice

22 e liver and spleen of susceptible mice after orogastric inoculation.

23 ociated lymph tissues of the mouse following orogastric inoculation.

24 failed to survive in the cecum of mice after orogastric inoculation.

25 nogenic in mice following intranasal but not orogastric inoculation.

26 In an orogastric model of Y. pseudotuberculosis infection, a D

27 to be free of H. pylori were vaccinated with orogastric (n = 4) or intramuscular (n = 5) urease.

28 le suspension (two 40-mg doses on day 1, via orogastric or nasogastric tube, and 40 mg each day there

29 to impact the virulence of this organism in orogastric or systemic infection models.

30 stem with murine neonates, using the natural orogastric route of transmission for the enteropathogen

31 tonometer was placed in the stomach via the orogastric route.

32 ssion of mouse beta -defensins (mBDs) 1-4 in orogastric tissues from germ-free (gf) and Candida albic

33 levels of beta -defensin gene expression in orogastric tissues from gf mice varied significantly bet

34 wth velocity, decreased transition time from orogastric to breast feeds, and increased postprandial m

35 Both groups were given ciprofloxacin by orogastric tube twice daily for 14 days, beginning 1-2 h

36 [11C]methylphenidate administered through an orogastric tube.

37 High-dose orogastric vaccination with M. microti resulted in a sta

38 ceptibilities of 7-day-old and adult mice to orogastric Y. enterocolitica infection were assessed in

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