Generation of novel cationic antimicrobial peptides from natural non-antimicrobial sequences by acid-amide substitution
<p>Abstract</p> <p>Background</p> <p>Cationic antimicrobial peptides (CAMPs) are well recognized to be promising as novel antimicrobial and antitumor agents. To obtain novel skeletons of CAMPs, we propose a simple strategy using acid-amide substitution (i.e. Glu→Gln, As...
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Main Authors: | , , , , , , |
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Format: | Book |
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BMC,
2011-03-01T00:00:00Z.
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Internet
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A1234.567 |
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Copy 1 | Available |