ライフサイエンスコーパス: ceca

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1 o showed a reduced ability to colonize chick ceca.

2 erial killing via an ion channel activity of CecA.

3 intestine and longer-term clearance from the ceca.

4 were increased approximately 2.5-fold in the ceca and colons of H. bilis-inoculated mice.

5 quantitatively detect H. hepaticus in mouse ceca and feces using the ABI Prism 7700 sequence detecti

6 gly expressed around ENCCs as they enter the ceca and hindgut.

7 cytoplasm of epithelial cells of the gastric ceca and posterior stomach.

8 ow decreased commensal colonization of chick ceca and reduced colonization of BALB/cByJ mice compared

9 centration of the enzyme was observed in the ceca, and a 7.5-fold concentration occurred in the excre

10 sults support a mechanism of action in which CecA binds to and covers the membrane surface, thereby c

11 eads to reduction in C. jeuni numbers in the ceca by nine weeks post infection.

12 of the insect antibiotic peptide cecropin A (CecA) in the phospholipid bilayer membrane was determine

13 lly, ET3, which is strongly expressed in the ceca, inhibits the chemoattraction of NCC to glial-deriv

14 -infected mice were colonized at high rates: ceca of 50/50 wild-type mice and 168/170 IL-10(-/-) mice

15 Helicobacter spp. were cultured from the ceca of 62 of 79 mice.

16 been isolated from the inflamed stomachs and ceca of adult Syrian hamsters.

17 Salmonella more rapidly clear the ceca of birds administered the modified probiotic than o

18 Ceca of C. jejuni 11168-infected mice were colonized at

19 At 16 wpi, the ceca of H. bilis-infected Rag2(-/-) mice treated with co

20 Analysis of the gene expression in ceca of H. hepaticus infected mice revealed 25 up-regula

21 e gamma-H2AX was significantly higher in the ceca of H. saguini-infected gnotobiotic mice than in the

22 , but IFN-gamma expression was normal in the ceca of IL-23p19-deficient mice during serotype Typhimur

23 nalysis of C. jejuni localization within the ceca of infected mice determined that the primary differ

24 athology scores was observed in the ilea and ceca of mice infected with the ibeA mutant.

25 tion of gamma interferon was observed in the ceca of mice infected with the ibeA mutant.

26 While H2 levels were greatly reduced in ceca of mice treated with antibiotics, both the Deltahyc

27 s Bacteroidetes populations long term in the ceca of mice, but the presence of C. albicans during cef

28 ells against microbial Ags isolated from the ceca of normal animals was observed.

29 At 18 h postchallenge, the ceca of resistant C57BL/6 mice were histologically unrem

30 causes an acute inflammatory reaction in the ceca of streptomycin-pretreated mice that involves T-cel

31 causes an acute inflammatory reaction in the ceca of streptomycin-pretreated mice.

32 cing microbial richness and diversity in the ceca of stressed mice.

33 in the commensal E. coli harvested from the ceca of the stressed mice.

34 thetaiotaomicron was then harvested from the ceca of these hosts during the suckling period (postnata

35 Furthermore, histology of the ceca revealed that mice administered IL-12 antisera fail

36 tion of the beta-glucanase isolated from the ceca testified to its origin from the transgenic barley.

37 as little effect on bacterial numbers in the ceca, the main site of colonisation, where C. jejuni per

38 ortantly, increased fibrin deposition in the ceca was not associated with increased plasma fibrin whe

39 s ineffective in clearing C. jejuni from the ceca within the production lifetime of chickens, althoug

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