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1 11-member cyclic peptide, whereas FK506 is a macrolide antibiotic.
2 rophylactic treatment with clarithromycin, a macrolide antibiotic.
3 e novel form of proarrhythmia seen with this macrolide antibiotic.
4 to the first total synthesis of this complex macrolide antibiotic.
5 hylamino)-3,4,6-trideoxyhexose found in some macrolide antibiotics.
6 ents with acute coronary syndrome when given macrolide antibiotics.
7 duct ions of explosives, acylcarnitines, and macrolide antibiotics.
8 ed activity of the broader spectrum group of macrolide antibiotics.
9 ng antibiotic resistance against a number of macrolide antibiotics.
10 Ketolides represent a new generation of macrolide antibiotics.
11 contributes to its ability to generate four macrolide antibiotics.
12 odular PKSs, which catalyze the synthesis of macrolide antibiotics.
13 ts ability to produce two distinct groups of macrolide antibiotics.
14 hrough genetic analysis to be susceptible to macrolide antibiotics.
15 nthesis may modulate site-specific action of macrolide antibiotics.
16 al cells treated with high concentrations of macrolide antibiotics.
17 tunnel is the target of clinically important macrolide antibiotics.
18 tcomes in a mouse model with beta-lactam and macrolide antibiotics.
19 increasingly resistant to currently marketed macrolide antibiotics.
20 s such as cyclosporin, statins, taxanes, and macrolide antibiotics.
21 clav, clindamycin, and fluoroquinolones) and macrolide antibiotics; a hand hygiene campaign; hospital
22 trE efflux pump system confers resistance to macrolide antibiotics and antimicrobial substances of th
23 iation pathways of a variety of ions such as macrolide antibiotics and hydrogen-bonded complexes.
24 rrent use of terfenadine and contraindicated macrolide antibiotics and imidazole antifungals continue
25 provides a platform for the discovery of new macrolide antibiotics and may also serve as the basis fo
26 atal cases were less likely to have received macrolide antibiotics and more likely to have received s
27 transporter has been implicated in efflux of macrolide antibiotics and secretion of enterotoxin STII.
28 S) genes: derivatives of medically important macrolide antibiotics and unusual polycyclic aromatic co
29 ition of carbamazepine metabolism by certain macrolide antibiotics, antifungals, verapamil, diltiazem
35 natives to erythromycin, including the newer macrolide antibiotics, are now part of the recommendatio
36 6-trideoxyhexose found, for example, in such macrolide antibiotics as erthyromycin, azithromycin, and
38 udy was to assess whether treatment with the macrolide antibiotic azithromycin improves endothelial f
41 assess whether short-term treatment with the macrolide antibiotic azithromycin reduces recurrent isch
45 giogenesis stimulation can be blocked by the macrolide antibiotic borrelidin (BN), which exhibits a b
46 resent a practical, fully synthetic route to macrolide antibiotics by the convergent assembly of simp
47 nt data challenged this view by showing that macrolide antibiotics can differentially affect synthesi
49 he potential anti-inflammatory activity of 3 macrolide antibiotics, clarithromycin, roxithromycin, an
52 somes, (ii) inhibition of CD4 degradation by macrolide antibiotics does not restore surface expressio
53 an antifungal drug of the family of polyene macrolide antibiotics, elevated YFP expression by the re
56 megalomicea and differs from the well-known macrolide antibiotic erythromycin by the addition of a u
57 oxyglucose, is an unusual sugar found on the macrolide antibiotic erythromycin, and it has been shown
61 intriguing class of mutants is resistant to macrolide antibiotics even though these drugs still bind
64 During antibiotic stewardship, use of 4C and macrolide antibiotics fell by 47% (mean decrease 224 def
66 ation and disease progression, we tested two macrolide antibiotics for their ability to inhibit Nef f
68 reviously to be involved in interaction with macrolide antibiotics, have been modeled in the crystall
71 site-specific oxidation of the precursors to macrolide antibiotics in the genus Streptomyces introduc
72 o)-3,4,6-trideoxyhexose found in a number of macrolide antibiotics including methymycin (2), neomethy
75 induced lethality and identified a series of macrolide antibiotics, including roxithromycin, that pot
76 ion leading to the production of a series of macrolide antibiotics, including the natural ketolides n
77 ptide sequence and the chemical structure of macrolide antibiotic, indicating possible interaction be
79 ing "plug-in-the-bottle" model suggests that macrolide antibiotics inhibit translation by binding ins
83 A key mechanism of bacterial resistance to macrolide antibiotics is the dimethylation of a nucleoti
88 - and 14-membered aglycone precursors of the macrolide antibiotics methymycin and picromycin, respect
89 nsferase involved in the biosynthesis of the macrolide antibiotics methymycin, neomethymycin, narbomy
92 oxidative tailoring of the 16-membered ring macrolide antibiotic mycinamicin II in the actinomycete
93 or the production of hybrid glycopeptide and macrolide antibiotics, novel anthelminthic agents and no
95 ed by prescription fills for a penicillin or macrolide antibiotic, or for trimethoprim-sulfamethoxazo
96 ycin was associated with previous use of any macrolide antibiotic (P < 0.001), and resistance to metr
99 MtrE multidrug-resistance efflux pump expels macrolide antibiotics, penicillin, and antimicrobial eff
103 ch as the prostanoids, indole alkaloids, and macrolide antibiotics, provide ample evidence for the en
106 The potent antiproliferative activity of the macrolide antibiotic rapamycin is known to involve bindi
107 t has been suggested that the ability of the macrolide antibiotic rapamycin to inhibit 4BP-1 phosphor
110 have demonstrated that chronic therapy with macrolide antibiotics reduces the morbidity of patients
111 erties of the ribosomal exit tunnel and that macrolide antibiotics reshape the cellular proteome rath
112 onas vaginalis Sequencing was used to assess macrolide antibiotic resistance among M. genitalium-posi
113 lly transmitted organisms, and high rates of macrolide antibiotic resistance in a diverse sample of s
114 transmitted organisms and the frequency of a macrolide antibiotic resistance phenotype were determine
119 reactionary sites which are complementary to macrolide antibiotic spiramycin (SPI) were synthetized b
123 ling in the presence of clinically important macrolide antibiotics, such as erythromycin, leading to
124 desosamine are aminohexoses found in several macrolide antibiotics, such as tylosin and methymycin, r
125 of which were predicted to be susceptible to macrolide antibiotics, suggesting that different strains
130 lav, and third-generation cephalosporins, or macrolide antibiotics that exceeded hospital-specific th
131 means to control the biological activity of macrolide antibiotics, the availability of macrolide gly
132 rate specificity of oxidative enzymes toward macrolide antibiotics, the x-ray structure of CYP154C1 f
134 Here we demonstrate that a single pulsed macrolide antibiotic treatment (PAT) course early in lif
139 not, which makes comparisons between these 2 macrolide antibiotics useful in assessing clinically imp
140 ide synthase (PKS) biosynthetic tailoring of macrolide antibiotics usually involves one or more oxida
141 uvenimicin, M-4365, and rosamicin classes of macrolide antibiotics via late-stage diversification.
142 and actively extrudes substrates, including macrolide antibiotics, virulence factors, peptides and c
143 The completion of the synthesis of the two macrolide antibiotics was accomplished by the union of t
145 xposure has ceased.High or multiple doses of macrolide antibiotics, when given early in life, can per
147 e observed after exposure to clindamycin and macrolide antibiotics, which have been proposed to targe
148 ion experiment over 25 days except for three macrolide antibiotics, which reached saturation at 300 n
150 , led to the discovery of gladiolin, a novel macrolide antibiotic with potent activity against Mycoba
154 our knowledge of the mode of interaction of macrolide antibiotics with their ribosomal target and of
155 eceptor (e.g., some anticancer compounds and macrolide antibiotics), with subsequent effects on trans
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