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Macrolides, lincosamides and streptogramins--early observations on their modes of action.

作者信息

Vázquez D

出版信息

J Antimicrob Chemother. 1985 Jul;16 Suppl A:225-6. doi: 10.1093/jac/16.suppl_a.225.

DOI:10.1093/jac/16.suppl_a.225
PMID:3932308
Abstract
摘要

相似文献

1
Macrolides, lincosamides and streptogramins--early observations on their modes of action.
J Antimicrob Chemother. 1985 Jul;16 Suppl A:225-6. doi: 10.1093/jac/16.suppl_a.225.
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[Resistance to macrolides, lincosamides and streptogramins in infections by Streptococcus pneumoniae].
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Inducible resistance to macrolides, lincosamides and streptogramin type B antibiotics: the resistance phenotype, its biological diversity, and structural elements that regulate expression--a review.对大环内酯类、林可酰胺类和B型链阳菌素类抗生素的诱导性耐药：耐药表型、其生物学多样性以及调控表达的结构元件——综述
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Gene heterogeneity for resistance to macrolides, lincosamides and streptogramins in Enterobacteriaceae.肠杆菌科细菌对大环内酯类、林可酰胺类及链阳菌素类耐药的基因异质性
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Bacterial resistance to macrolide, lincosamide, and streptogramin antibiotics by target modification.细菌通过靶点修饰对大环内酯类、林可酰胺类和链阳菌素类抗生素产生耐药性。
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Intrinsic and unusual resistance to macrolide, lincosamide, and streptogramin antibiotics in bacteria.细菌对大环内酯类、林可酰胺类和链阳菌素类抗生素的内在及异常耐药性。
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[Classification, structure, pharmacokinetic and mode of action of macrolides, lincosamides and streptogramins. Resistance phenomena].[大环内酯类、林可酰胺类及链阳菌素类的分类、结构、药代动力学及作用方式。耐药现象]
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Binding parameters and microbiological activity of macrolides, lincosamides and streptogramins against Staphylococcus aureus.大环内酯类、林可酰胺类及链阳菌素类药物对金黄色葡萄球菌的结合参数及微生物活性
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Lincosamide antibiotics stimulate dissociation of peptidyl-tRNA from ribosomes.林可酰胺类抗生素可刺激肽基 - tRNA从核糖体上解离。
Antimicrob Agents Chemother. 1993 Sep;37(9):2027-9. doi: 10.1128/AAC.37.9.2027.
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Erythromycin, lincosamides, peptidyl-tRNA dissociation, and ribosome editing.红霉素、林可酰胺类、肽基-tRNA解离与核糖体校正
Mol Gen Genet. 1994 Apr;243(2):225-33. doi: 10.1007/BF00280320.