| pubmed-article:10223949 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:10223949 | lifeskim:mentions | umls-concept:C0030956 | lld:lifeskim |
| pubmed-article:10223949 | lifeskim:mentions | umls-concept:C0184511 | lld:lifeskim |
| pubmed-article:10223949 | lifeskim:mentions | umls-concept:C0441655 | lld:lifeskim |
| pubmed-article:10223949 | lifeskim:mentions | umls-concept:C0444669 | lld:lifeskim |
| pubmed-article:10223949 | lifeskim:mentions | umls-concept:C1136254 | lld:lifeskim |
| pubmed-article:10223949 | lifeskim:mentions | umls-concept:C0218144 | lld:lifeskim |
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| pubmed-article:10223949 | lifeskim:mentions | umls-concept:C0599473 | lld:lifeskim |
| pubmed-article:10223949 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:10223949 | pubmed:dateCreated | 1999-5-27 | lld:pubmed |
| pubmed-article:10223949 | pubmed:abstractText | N-acylated or D enantiomer peptide derivatives based on the sequence RRWQWRMKK in lactoferricin B demonstrated antimicrobial activities greater than those of lactoferricin B against bacteria and fungi. The most potent peptide, conjugated with an 11-carbon-chain acyl group, showed two to eight times lower MIC than lactoferricin B. | lld:pubmed |
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| pubmed-article:10223949 | pubmed:language | eng | lld:pubmed |
| pubmed-article:10223949 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10223949 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:10223949 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:10223949 | pubmed:month | May | lld:pubmed |
| pubmed-article:10223949 | pubmed:issn | 0066-4804 | lld:pubmed |
| pubmed-article:10223949 | pubmed:author | pubmed-author:HashimotoKK | lld:pubmed |
| pubmed-article:10223949 | pubmed:author | pubmed-author:TakaseMM | lld:pubmed |
| pubmed-article:10223949 | pubmed:author | pubmed-author:MatsumotoHH | lld:pubmed |
| pubmed-article:10223949 | pubmed:author | pubmed-author:WakabayashiHH | lld:pubmed |
| pubmed-article:10223949 | pubmed:author | pubmed-author:TeraguchiSS | lld:pubmed |
| pubmed-article:10223949 | pubmed:author | pubmed-author:HayasawaHH | lld:pubmed |
| pubmed-article:10223949 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:10223949 | pubmed:volume | 43 | lld:pubmed |
| pubmed-article:10223949 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:10223949 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:10223949 | pubmed:pagination | 1267-9 | lld:pubmed |
| pubmed-article:10223949 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
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| pubmed-article:10223949 | pubmed:year | 1999 | lld:pubmed |
| pubmed-article:10223949 | pubmed:articleTitle | N-Acylated and D enantiomer derivatives of a nonamer core peptide of lactoferricin B showing improved antimicrobial activity. | lld:pubmed |
| pubmed-article:10223949 | pubmed:affiliation | Nutritional Science Laboratory, Morinaga Milk Industry Co., Ltd., Zama, Kanagawa 228-8583, Japan. Hiroyuki_Wa@msn.com | lld:pubmed |
| pubmed-article:10223949 | pubmed:publicationType | Journal Article | lld:pubmed |
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