ライフサイエンスコーパス: anaerobic culture

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1 cimen (preferably of tissue) for aerobic and anaerobic culture.

2 evaluate the microbiota of severe ECC using anaerobic culture.

3 stationary-phase survival and recovery from anaerobic culture.

4 M. Alden Research Laboratory for aerobic and anaerobic culture.

5 fficile in stool specimens was determined by anaerobic culture.

6 Quantitative anaerobic cultures also detect high quantities of anaero

7 nd community composition were analyzed using anaerobic culture and 16S rDNA pyrosequencing.

8 crobial identification was carried out using anaerobic culture and 16S rRNA-based PCR identification

9 ty in the mutant strain was not repressed in anaerobic cultures as reported previously for the parent

10 e test performed equally well on aerobic and anaerobic culture broth.

11 associated with this uptake was repressed in anaerobic cultures but was rapidly induced by exposure o

12 nt with this, addition of a ROS scavenger or anaerobic culture conditions also worked to promote L-fo

13 utility is limited due to the requirement of anaerobic culture conditions and microbiological experti

14 tions) were compared to those of CDBB (under anaerobic culture conditions) for the recovery of C. dif

15 environmental samples, without the need for anaerobic culture conditions.

16 We conclude that anaerobic culture detected as wide a diversity of specie

17 When mRNA levels of aerobic and anaerobic cultures during exponential growth were compar

18 ro Cd assay and a standard CCCNA compared to anaerobic culture for the detection of toxigenic C. diff

19 culture-independent molecular techniques and anaerobic cultures have broadened our view of CF airway

20 genomic sequencing with standard aerobic and anaerobic culture in 97 sonication fluid samples from pr

21 Anaerobic culture is employed routinely in the primary i

22 uggests that the presence of ferrous iron in anaerobic culture media exacerbates the toxicity of hydr

23 of 13 days to be applied to both aerobic and anaerobic culture media for all periprosthetic specimens

24 nded culture incubation been applied only to anaerobic culture media.

25 ficant induction is observed in a continuous anaerobic culture of human fecal bacteria, suggesting th

26 that sboX is induced in stationary phase of anaerobic cultures of JH642.

27 Anaerobic cultures of Shewanella oneidensis MR-1 grown w

28 We then used IgA-SEQ and extensive anaerobic culturing of fecal bacteria from IBD patients

29 A total of 32 proteins from anaerobic cultures show pH-dependent expression, and onl

30 ated at 35 degrees C for 5 to 7 days in each anaerobic culture system.

31 ack system compared with that of established anaerobic culturing techniques was similar and significa

32 In this report, we combine high-throughput anaerobic culturing techniques with gnotobiotic animal h

33 laboratory lacking resources for traditional anaerobic culturing techniques.

34 Relative to toxigenic anaerobic culture, the sensitivity, specificity, and pos

35 For anaerobic cultures, the times were 90.8 and 45 h, respec

36 For anaerobic cultures, these times were 45.1 and 9.9 h, res

37 utility of the platform for both aerobic and anaerobic culture, three bacteria with differential oxyg

38 inoculated in 10-ml aliquots to aerobic and anaerobic culture vials.

39 jects positive for C. difficile by toxigenic anaerobic culture were asked to submit additional specim

40 etabolic by-product secretion in aerobic and anaerobic culture were consistent with experimental data

41 Standard aerobic and aerobic-anaerobic cultures were negative.

42 Quantitative aerobic and anaerobic cultures were obtained from 24 premenopausal w

43 tinal simulator) comprised a continuous-flow anaerobic culture which was inoculated with fecal sample

44 or nitrite metabolism, or (ii) flushing the anaerobic culture with argon (which should purge it of n

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