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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.
9                                              Glycopeptide antibiotics are widely used in the treatmen
10 ichia coli, which is never challenged by the glycopeptide antibiotics because they cannot penetrate t
11             All the inducers identified were glycopeptide antibiotics, but teicoplanin, a membrane-an
12 -Ala cell wall precursor to d-Ala-d-Lac upon glycopeptide antibiotic challenge, displaying a potency
13                           Bleomycin (BLM), a glycopeptide antibiotic chemotherapy agent, is capable o
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.
16                                 Like certain glycopeptide antibiotics (e.g., vancomycin), PGRPs kill
17                     The adamantyl-2 amide of glycopeptide antibiotic eremomycin (1a in Chart 1, AN090
18                                              Glycopeptide antibiotics (GPAs) are nonribosomal peptide
19                                     Although glycopeptide antibiotics (GPAs), including vancomycin an
20        Chloroeremomycin, a vancomycin family glycopeptide antibiotic has three sugars, one D-glucose
21                     The vancomycin family of glycopeptide antibiotics has been inspiring research in
22                                              Glycopeptide antibiotics have long served as drugs of la
23                                           In glycopeptide antibiotics, however, these cooperative pro
24                      VanA-type resistance to glycopeptide antibiotics in clinical enterococci is regu
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
28                                       In the glycopeptide antibiotic producers Streptomyces toyocaens
29                            Second-generation glycopeptide antibiotics similar to vancomycin are in cl
30 ramoplanin is structurally less complex than glycopeptide antibiotics such as vancomycin, peptidomime
31  distinct hydroxyl groups within the complex glycopeptide antibiotic teicoplanin A2-2.
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
38                              Vancomycin is a glycopeptide antibiotic used for the treatment of Gram-p
39                    The sugar residues of the glycopeptide antibiotic vancomycin contribute to the coo
40 ly established dimerization of the important glycopeptide antibiotic vancomycin in four different aqu
41 sors in bacteria, which are resistant to the glycopeptide antibiotic vancomycin.
42  dipeptidase essential for resistance to the glycopeptide antibiotic vancomycin.
43                     The structurally related glycopeptide antibiotics vancomycin, ristocetin A, and t
44                                  Using three glycopeptide antibiotics, vancomycin, teicoplanin, and t
45                       Oritavancin is a novel glycopeptide antibiotic with concentration-dependent kil
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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