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1 ere positively selected in medium containing geneticin.
2 nce of high concentrations of the antibiotic geneticin.
3 thine (d-Orn), a substrate analog, and G418 (Geneticin), a weak non-competitive inhibitor, was determ
4                   By contrast, we found that geneticin, a ribosome-binding antibiotic with translatio
5 ht PTC-containing XP-C cells, treatment with Geneticin and gentamicin resulted in (i) stabilized XPC-
6                 We treated the colonies with geneticin and mechanically isolated hFLMPCs, which were
7 s determined after prolonged culture without geneticin and on irradiated cells.
8  Chinese hamster ovary cells, selection with Geneticin, and amplification with methotrexate, a cell l
9 ression even after prolonged culture without geneticin, and on irradiated tumor cells.
10  for selection of stable transfectants using Geneticin, and the presence of plasmid in transfectants
11  2-DOS aminoglycosides paromomycin and G418 (geneticin) are compared, using both human and Escherichi
12 om complexes of paromomycin, tobramycin, and Geneticin bound to an A-site oligonucleotide, and paromo
13                           After selection in Geneticin, clones of pinin-transfected cells were isolat
14                               Treatment with geneticin elicits a multiday response, and residual F9 a
15 aminoglycoside antibiotic read-through agent geneticin (G418) across a diverse range of in vitro repo
16 vidence is now available that gentamicin and Geneticin (G418) can induce the mammalian ribosome to su
17 found that doxycycline, chloramphenicol, and Geneticin (G418) interfered with insertion of selenocyst
18                                              Geneticin (G418) was then identified as a potent inducer
19  a model of the Leishmania ribosomal A site: Geneticin (G418), a potent aminoglycoside for the treatm
20 he 80S ribosome in complex with paromomycin, geneticin (G418), gentamicin, and TC007, solved at 3.3-
21 odial inhibitors in culture, blasticidin and geneticin (G418), were selected for further study.
22 lls in modified minimal media that contained geneticin (G418).
23       Application of IQSCMaRTEA reveals that geneticin is much more efficacious in vivo than gentamic
24                                 Furthermore, geneticin, its metabolites, or better tolerated analogue
25 rt that paromomycin and the related compound geneticin manifest their major in vitro anti-C. parvum a
26 ponsiveness to the readthrough-inducing drug geneticin of 11 rationally selected factor IX (FIX) nons
27 two aminoglycoside antibiotics, neomycin and Geneticin, on the endocytic pathway were studied using a
28 stance gene on the vector was used to create geneticin-resistant stable cell lines.
29                                              Geneticin selection of BHK-21 cells transfected with Rlu
30 slation fidelity antibiotics paromomycin and geneticin, to high salt and calcium concentrations, to p

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