ライフサイエンスコーパス: Gram staining

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1 ent infections without organisms detected by Gram staining.

2 exhibiting Gram-positive cocci upon initial Gram staining.

3 microbiological methods, such as culture and gram staining.

4 urease, catalase, and oxidase reactions and Gram staining.

5 onial morphology on CCFA, or morphology upon Gram staining.

6 acity could be observed visually, only after Gram staining.

7 MRSA on TSA II was confirmed by Gram staining, a coagulase test, and a cefoxitin disk te

8 When the LFA was paired with Gram staining, a sensitivity of 100% was achieved after

9 Gram staining, acid-fast staining, and lactic acid, cryp

10 m direct and extracted culture methods using Gram staining and a GAS-specific latex agglutination tes

11 Gram staining and fluorescence in situ hybridization ide

12 lection of two corneal scrapes, one used for Gram staining and the other transported in BHI followed

13 Gram staining, bright-field microscopy, hematoxylin and

14 Based on gram staining, colony characteristics, biochemical react

15 ed for gram-negative bacilli and examined by Gram staining for both sputum adequacy (using the qualit

16 when only one of two cultures is positive by Gram staining for staphylococci.

17 lture bottles in which yeast was observed by Gram staining (herein referred to as yeast-positive bloo

18 ues for bacteria including quantitative PCR, Gram staining, immunofluorescence and in situ hybridizat

19 No organisms were seen by Gram staining in 225 (62%) of the ETAs.

20 th comprehensive bacteriology is superior to Gram staining in identifying pathogens in CF sputum.

21 erent bacteria in each case was performed by Gram staining, in situ hybridization using fluorescence-

22 of our findings, the absence of organisms on Gram staining is a useful criterion for rejecting ETAs f

23 The results of Gram staining of a vaginal smear were consistent with BV

24 These organisms can be seen upon Gram staining of clinical specimens or can be isolated a

25 The phenotype-based scheme included Gram staining of growth on BEAA and subculture of cocci

26 of a composite reference standard comprising Gram staining of sputum samples and sputum/blood culture

27 hotypes per high-power field, as detected by Gram staining of vaginal swab specimens.

28 Gram staining offered rapid validation of enhanced bindi

29 es as the structure of the cell envelope and Gram-staining pattern.

30 Gram staining quickly eliminated gram-positive bacilli f

31 electron microscopy, LIVE/DEAD staining, and Gram staining revealed a difference in the distributions

32 Accordingly, Gram staining revealed bacteria within peritoneal fluids

33 Sequencing of 16S PCR products and Gram staining showed that the majority of bacteria in th

34 tified by conventional methods that included Gram staining, tests for colonial morphology, tests for

35 culture bottles newly positive for yeast by Gram staining was performed at five hospitals.

36 ontained Gram-negative bacilli identified by Gram staining, we isolated bacterial DNA using spin colu

37 tles) with Gram-positive cocci observed with Gram staining were analyzed using the BC-GP assay.

38 lture bottles with GPC seen in clusters with Gram staining were tested using the BNSA test and a dire

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