コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 11-member cyclic peptide, whereas FK506 is a macrolide antibiotic.
2 rophylactic treatment with clarithromycin, a macrolide antibiotic.
3 translocation pathways for a bile acid and a macrolide antibiotic.
4 Tylosin is a broad-spectrum macrolide antibiotic.
5 e novel form of proarrhythmia seen with this macrolide antibiotic.
6 to the first total synthesis of this complex macrolide antibiotic.
7 s such as cyclosporin, statins, taxanes, and macrolide antibiotics.
8 hylamino)-3,4,6-trideoxyhexose found in some macrolide antibiotics.
9 ents with acute coronary syndrome when given macrolide antibiotics.
10 duct ions of explosives, acylcarnitines, and macrolide antibiotics.
11 ed activity of the broader spectrum group of macrolide antibiotics.
12 ng antibiotic resistance against a number of macrolide antibiotics.
13 Ketolides represent a new generation of macrolide antibiotics.
14 contributes to its ability to generate four macrolide antibiotics.
15 odular PKSs, which catalyze the synthesis of macrolide antibiotics.
16 ts ability to produce two distinct groups of macrolide antibiotics.
17 insights for future development of improved macrolide antibiotics.
18 ally involved in the biosynthesis of diverse macrolide antibiotics.
19 hat it would overlap with the ribosome-bound macrolide antibiotics.
20 hrough genetic analysis to be susceptible to macrolide antibiotics.
21 nthesis may modulate site-specific action of macrolide antibiotics.
22 al cells treated with high concentrations of macrolide antibiotics.
23 tunnel is the target of clinically important macrolide antibiotics.
24 tcomes in a mouse model with beta-lactam and macrolide antibiotics.
25 increasingly resistant to currently marketed macrolide antibiotics.
26 clav, clindamycin, and fluoroquinolones) and macrolide antibiotics; a hand hygiene campaign; hospital
29 trE efflux pump system confers resistance to macrolide antibiotics and antimicrobial substances of th
30 iation pathways of a variety of ions such as macrolide antibiotics and hydrogen-bonded complexes.
31 rrent use of terfenadine and contraindicated macrolide antibiotics and imidazole antifungals continue
32 provides a platform for the discovery of new macrolide antibiotics and may also serve as the basis fo
33 atal cases were less likely to have received macrolide antibiotics and more likely to have received s
34 transporter has been implicated in efflux of macrolide antibiotics and secretion of enterotoxin STII.
35 one-year study on the occurrence and fate of macrolide antibiotics and their metabolites, synthesis b
36 S) genes: derivatives of medically important macrolide antibiotics and unusual polycyclic aromatic co
37 ition of carbamazepine metabolism by certain macrolide antibiotics, antifungals, verapamil, diltiazem
43 natives to erythromycin, including the newer macrolide antibiotics, are now part of the recommendatio
44 6-trideoxyhexose found, for example, in such macrolide antibiotics as erthyromycin, azithromycin, and
47 udy was to assess whether treatment with the macrolide antibiotic azithromycin improves endothelial f
51 assess whether short-term treatment with the macrolide antibiotic azithromycin reduces recurrent isch
57 giogenesis stimulation can be blocked by the macrolide antibiotic borrelidin (BN), which exhibits a b
58 Moreover, high-resolution structures of two macrolide antibiotics bound to the unmodified ribosome r
59 resent a practical, fully synthetic route to macrolide antibiotics by the convergent assembly of simp
60 nt data challenged this view by showing that macrolide antibiotics can differentially affect synthesi
62 an opportunity to potentially repurpose the macrolide antibiotic clarithromycin to treat tuberculosi
63 ing reports regarding the association of the macrolide antibiotic clarithromycin with cardiovascular
64 he potential anti-inflammatory activity of 3 macrolide antibiotics, clarithromycin, roxithromycin, an
66 patient group with common coprescription of macrolide antibiotics.Conclusions: This pilot study supp
68 somes, (ii) inhibition of CD4 degradation by macrolide antibiotics does not restore surface expressio
70 an antifungal drug of the family of polyene macrolide antibiotics, elevated YFP expression by the re
73 megalomicea and differs from the well-known macrolide antibiotic erythromycin by the addition of a u
74 oxyglucose, is an unusual sugar found on the macrolide antibiotic erythromycin, and it has been shown
78 intriguing class of mutants is resistant to macrolide antibiotics even though these drugs still bind
81 During antibiotic stewardship, use of 4C and macrolide antibiotics fell by 47% (mean decrease 224 def
82 as many commonly used drug classes, such as macrolide antibiotics, fluoroquinolone antibiotics, anti
84 ation and disease progression, we tested two macrolide antibiotics for their ability to inhibit Nef f
85 ermination of azithromycin, a broad-spectrum macrolide antibiotic, from various biological samples (u
86 Growing resistance toward ribosome-targeting macrolide antibiotics has limited their clinical utility
88 reviously to be involved in interaction with macrolide antibiotics, have been modeled in the crystall
91 nd, randomised, placebo-controlled trials of macrolide antibiotics in adult patients with bronchiecta
92 site-specific oxidation of the precursors to macrolide antibiotics in the genus Streptomyces introduc
94 o)-3,4,6-trideoxyhexose found in a number of macrolide antibiotics including methymycin (2), neomethy
98 induced lethality and identified a series of macrolide antibiotics, including roxithromycin, that pot
99 ion leading to the production of a series of macrolide antibiotics, including the natural ketolides n
100 ptide sequence and the chemical structure of macrolide antibiotic, indicating possible interaction be
102 ing "plug-in-the-bottle" model suggests that macrolide antibiotics inhibit translation by binding ins
107 A key mechanism of bacterial resistance to macrolide antibiotics is the dimethylation of a nucleoti
113 - and 14-membered aglycone precursors of the macrolide antibiotics methymycin and picromycin, respect
114 nsferase involved in the biosynthesis of the macrolide antibiotics methymycin, neomethymycin, narbomy
117 oxidative tailoring of the 16-membered ring macrolide antibiotic mycinamicin II in the actinomycete
118 or the production of hybrid glycopeptide and macrolide antibiotics, novel anthelminthic agents and no
120 lipidemic medications (OR = 0.39, P = .004), macrolide antibiotics (OR = 0.40, P = .03), and calcium
121 ed by prescription fills for a penicillin or macrolide antibiotic, or for trimethoprim-sulfamethoxazo
122 ycin was associated with previous use of any macrolide antibiotic (P < 0.001), and resistance to metr
125 MtrE multidrug-resistance efflux pump expels macrolide antibiotics, penicillin, and antimicrobial eff
126 The total synthesis of the potent polyene macrolide antibiotic pentamycin was accomplished by an e
127 epoxidation of 4,5-desepoxypimaricin to the macrolide antibiotic, pimaricin, reveals key catalytic s
132 ch as the prostanoids, indole alkaloids, and macrolide antibiotics, provide ample evidence for the en
135 The potent antiproliferative activity of the macrolide antibiotic rapamycin is known to involve bindi
136 t has been suggested that the ability of the macrolide antibiotic rapamycin to inhibit 4BP-1 phosphor
140 have demonstrated that chronic therapy with macrolide antibiotics reduces the morbidity of patients
141 erties of the ribosomal exit tunnel and that macrolide antibiotics reshape the cellular proteome rath
142 onas vaginalis Sequencing was used to assess macrolide antibiotic resistance among M. genitalium-posi
143 lly transmitted organisms, and high rates of macrolide antibiotic resistance in a diverse sample of s
144 transmitted organisms and the frequency of a macrolide antibiotic resistance phenotype were determine
149 reactionary sites which are complementary to macrolide antibiotic spiramycin (SPI) were synthetized b
154 ling in the presence of clinically important macrolide antibiotics, such as erythromycin, leading to
155 desosamine are aminohexoses found in several macrolide antibiotics, such as tylosin and methymycin, r
156 of which were predicted to be susceptible to macrolide antibiotics, suggesting that different strains
161 lav, and third-generation cephalosporins, or macrolide antibiotics that exceeded hospital-specific th
162 means to control the biological activity of macrolide antibiotics, the availability of macrolide gly
163 rate specificity of oxidative enzymes toward macrolide antibiotics, the x-ray structure of CYP154C1 f
165 Here we demonstrate that a single pulsed macrolide antibiotic treatment (PAT) course early in lif
170 not, which makes comparisons between these 2 macrolide antibiotics useful in assessing clinically imp
171 ide synthase (PKS) biosynthetic tailoring of macrolide antibiotics usually involves one or more oxida
172 uvenimicin, M-4365, and rosamicin classes of macrolide antibiotics via late-stage diversification.
173 and actively extrudes substrates, including macrolide antibiotics, virulence factors, peptides and c
174 The completion of the synthesis of the two macrolide antibiotics was accomplished by the union of t
176 xposure has ceased.High or multiple doses of macrolide antibiotics, when given early in life, can per
178 e observed after exposure to clindamycin and macrolide antibiotics, which have been proposed to targe
179 ion experiment over 25 days except for three macrolide antibiotics, which reached saturation at 300 n
183 , led to the discovery of gladiolin, a novel macrolide antibiotic with potent activity against Mycoba
185 ally contribute to a new generation of novel macrolide antibiotics with enhanced antifungal and/or an
188 our knowledge of the mode of interaction of macrolide antibiotics with their ribosomal target and of
189 eceptor (e.g., some anticancer compounds and macrolide antibiotics), with subsequent effects on trans