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1 pearing three to seven days after plating on selective medium).
2  the cultures are rinsed and placed on solid selective medium.
3 ydrolyzed esculin; and grew on Campylobacter selective medium.
4 er aztreonam or ceftazidime were used as the selective medium.
5 olonies were identified by their survival in selective medium after electroporation of correcting DNA
6 ferent methods: (i) plating on Thayer-Martin selective medium and testing by conventional microbiolog
7 med cell lines after 6 weeks of culturing in selective medium, and in these cell lines mtDNA was not
8              First, the stool is plated on a selective medium, and then suspected colonies are analyz
9 nificantly improved recovery after growth in selective medium as well as a significant increase in AT
10  be cultured for Escherichia coli O157:H7 on selective medium as well as that testing for the presenc
11  heterokaryotic transformant was observed on selective medium containing hygromycin B, neither germin
12 very of herbicide-resistant tobacco cells on selective medium, DNA sequence analyses identified base
13  (CCFA), which is an effective but expensive selective medium for C. difficile.
14                                        A new selective medium for rapidly growing mycobacteria (RGM m
15 uggest that CDBB-TC provides a sensitive and selective medium for the recovery of C. difficile organi
16 citrate bile salts sucrose agar, the primary selective medium for V. cholerae.
17                          In their respective selective mediums, growth of MPA-resistant (MPA(R)) isol
18 d by these patients were investigated with a selective medium incorporating vancomycin, imipenem, and
19          Leaky mutants, which grew slowly on selective medium, produced late revertants whereas tight
20 erefore, direct plating of rectal swabs onto selective medium proved to be a sensitive and cost-effec
21 rticipant in diabetic foot ulcers, we used a selective medium to culture both lower- and upper-extrem
22 n-dalfopristin-resistant E. faecium, we used selective medium to culture samples from chickens purcha
23 , respectively, was developed as an improved selective medium to isolate B. parapertussis from the na
24 lowed to set seed which are then plated on a selective medium to screen for transformants.
25                   Two rounds of isolation on selective medium were sufficient to obtain gene conversi