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1 lastid biogenesis inhibitors norflurazon and lincomycin.
2 s affected by treatment with norflurazon and lincomycin.
3  dramatically accelerated in the presence of lincomycin.
4                             The structure of lincomycin A consists of the unusual eight-carbon thiosu
5                                              Lincomycin A is a clinically useful antibiotic isolated
6                                              Lincomycin A is a potent antimicrobial agent noted for i
7 aliana plants under long-term treatment with lincomycin, a chloroplast protein synthesis inhibitor.
8 t and to inhibitors, such as norflurazon and lincomycin, affecting plastid signaling.
9 plastid signals, the effects of norflurazon, lincomycin and 3-(3,4-dichlorophenyl)-1,1-dimethylurea (
10  under a variety of treatments (Norflurazon, lincomycin and a far-red light pre-treatment) leading to
11  and partially GriH from the biosyntheses of lincomycin and griselimycin, respectively, also reduce t
12 sin contributed most to the risk followed by lincomycin and trimethoprim.
13 ty to doxycycline, and low susceptibility to lincomycin and tylosin.
14 ring resistance to kanamycin, spectinomycin, lincomycin, and gentamycin/sisomycin, respectively) were
15 ndent transcripts is specifically induced by lincomycin, and the splicing of ndhB transcripts is sign
16 at all three antibiotics (chlortetracycline, lincomycin, and tiamulin) and seven out of the ten genes
17 dochii to tiamulin, valnemulin, doxycycline, lincomycin, and tylosin by broth microdilution and that
18 lated, cia5-2, ispF and ispG albino mutants, lincomycin-, and norflurazon-treated).
19 results provide significant insight into the lincomycin biosynthetic pathway, because the activated o
20 ions completes the description of the entire lincomycin biosynthetic pathway.
21 e showed that treatment with norflurazon and lincomycin, but not DCMU, decreased the accumulation of
22 ycin), macrolides-lincosamids (erythromycin, lincomycin), coumarin derivatives (coumermycin A(1), nov
23 ein synthesis was blocked by the addition of lincomycin, D1 degradation was again slower in S264P tha
24                                    Moreover, lincomycin-dependent changes in LIGHT HARVESTING CHLOROP
25 ml chloramphenicol, gentamycin, paromomycin, lincomycin, hygromycin, and tetracycline, as well as cyc
26                    In this study, core-shell lincomycin-imprinted polymers were successfully synthesi
27 s used for pre-concentration and clean-up of lincomycin in the milk matrix prior to analysis via high
28             The linear range for analysis of lincomycin in the milk matrix using introduced method wa
29 identified, lin, which confers resistance to lincomycin, is the most prevalent, followed by mprF, sul
30 IP-based electrochemical sensor designed for Lincomycin (LIN) was fabricated using an electropolymeri
31  either 5 days of adjunctive clindamycin (or lincomycin) or no adjunctive antibiotic therapy alongsid
32 librated CSMISPE-HPLC-UV method was used for lincomycin residue checking and quantification in the pa
33  B. thetaiotaomicron, the homolog of linA, a lincomycin resistance gene from Staphylococcus aureus.
34 red to confer sensitivity to norflurazon and lincomycin, suggesting post-transcriptional regulation.
35  use antibiotics (trimethoprim, tylosin, and lincomycin) to algal and cyanobacterial species in Europ
36 nd ndhD-2 is completely lost in roots and in lincomycin-treated seedlings.
37         Inhibition of the D1 repair cycle by lincomycin treatment indicated that these plants experie
38 nt and a second mutant that was resistant to lincomycin, trimethoprim, or rifampin.
39 rmation of the fully saturated APD moiety of lincomycin versus the unsaturated APD moiety of PBDs, pr