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1 tential role of each residue of this complex glycopeptide antibiotic.
2 is highly reproducible and selective toward glycopeptide antibiotics.
3 larization based method for the detection of glycopeptide antibiotics.
4 activities, and probably the structures, of glycopeptide antibiotics.
5 to desolvation of the ligand binding site in glycopeptide antibiotics.
6 the vancomycin and the teicoplanin class of glycopeptide antibiotics.
7 omycin, a member of the vancomycin family of glycopeptide antibiotics.
8 rinsic resistance to the vancomycin class of glycopeptide antibiotics.
10 ichia coli, which is never challenged by the glycopeptide antibiotics because they cannot penetrate t
12 -Ala cell wall precursor to d-Ala-d-Lac upon glycopeptide antibiotic challenge, displaying a potency
14 ible for biosynthesis of the vancomycin-type glycopeptide antibiotic chloroeremomycin was recently se
15 es seen in three other crystal structures of glycopeptide antibiotics complexed with peptide ligands.
25 ence of resistance to vancomycin and related glycopeptide antibiotics is spurring efforts to develop
26 e bleomycins (BLMs) are structurally related glycopeptide antibiotics isolated from Streptomyces vert
27 to protoplasts that were pretreated with the glycopeptide antibiotic phleomycin, a nonspecific DNA do
30 ramoplanin is structurally less complex than glycopeptide antibiotics such as vancomycin, peptidomime
32 quantitate the binding affinity between the glycopeptide antibiotics teicoplanin from Actinoplanes t
33 results suggest new strategies for designing glycopeptide antibiotics that overcome bacterial resista
34 e essential to understanding the activity of glycopeptide antibiotics, the recognition of pathogens b
35 ed total syntheses of vancomycin and related glycopeptide antibiotics, their agylcons, and key analog
36 internuclear distances from the 19F of this glycopeptide antibiotic to natural-abundance 31P and to
37 nked the Lys-D-Ala-D-Ala binding epitope for glycopeptide antibiotics to three different carrier prot
40 ly established dimerization of the important glycopeptide antibiotic vancomycin in four different aqu
46 al component of the mannopeptimycins, cyclic glycopeptide antibiotics with activity against drug-resi
47 ycin, and we show that the activity of other glycopeptide antibiotics with this feature can also be s
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