Combining Topology and Sequence Design for the Discovery of Potent Antimicrobial Peptide Dendrimers against Multidrug-ResistantPseudomonas aeruginosa-Reference-Cited by-同舟云学术

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Combining Topology and Sequence Design for the Discovery of Potent Antimicrobial Peptide Dendrimers against Multidrug-ResistantPseudomonas aeruginosa

Published:2014-10-24 Issue:47 Volume:53 Page:12827-12831
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Stach Michaela,Siriwardena Thissa N.,Köhler Thilo,van Delden Christian,Darbre Tamis,Reymond Jean-Louis

Funder

University of Bern

Swiss National Science Foundation

European Marie Curie Initial Training Network BioChemLig

Swiss TransMed

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference53 articles.

1. Responses of Pseudomonas aeruginosa to antimicrobials

2. Platforms for antibiotic discovery

3. Antibiotics in the clinical pipeline in 2013

4. Combating Multidrug-Resistant Bacteria: Current Strategies for the Discovery of Novel Antibacterials

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