pubmed-article:10471587 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:10471587 | lifeskim:mentions | umls-concept:C0008151 | lld:lifeskim |
pubmed-article:10471587 | lifeskim:mentions | umls-concept:C0025663 | lld:lifeskim |
pubmed-article:10471587 | lifeskim:mentions | umls-concept:C0035379 | lld:lifeskim |
pubmed-article:10471587 | lifeskim:mentions | umls-concept:C0427965 | lld:lifeskim |
pubmed-article:10471587 | lifeskim:mentions | umls-concept:C1697858 | lld:lifeskim |
pubmed-article:10471587 | pubmed:issue | 9 | lld:pubmed |
pubmed-article:10471587 | pubmed:dateCreated | 1999-11-4 | lld:pubmed |
pubmed-article:10471587 | pubmed:abstractText | The conventional method for antimicrobial susceptibility testing of Chlamydia trachomatis is subjective and potentially misleading. We have developed a reverse transcriptase PCR (RT-PCR)-based method which is more sensitive and less subjective than the conventional method. Using 16 strains of C. trachomatis in triplicate assays, we found the RT-PCR method consistently more sensitive than the conventional technique for all eight antimicrobials tested, with resultant MICs determined by RT-PCR ranging from 1.6-fold higher (erythromycin) to >/=195-fold higher (amoxicillin). | lld:pubmed |
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pubmed-article:10471587 | pubmed:language | eng | lld:pubmed |
pubmed-article:10471587 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10471587 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:10471587 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:10471587 | pubmed:month | Sep | lld:pubmed |
pubmed-article:10471587 | pubmed:issn | 0066-4804 | lld:pubmed |
pubmed-article:10471587 | pubmed:author | pubmed-author:KinghornG RGR | lld:pubmed |
pubmed-article:10471587 | pubmed:author | pubmed-author:HARTV KVK | lld:pubmed |
pubmed-article:10471587 | pubmed:author | pubmed-author:HawkeyP MPM | lld:pubmed |
pubmed-article:10471587 | pubmed:author | pubmed-author:OxleyK MKM | lld:pubmed |
pubmed-article:10471587 | pubmed:author | pubmed-author:CrossN ANA | lld:pubmed |
pubmed-article:10471587 | pubmed:author | pubmed-author:KellockD JDJ | lld:pubmed |
pubmed-article:10471587 | pubmed:author | pubmed-author:Taraktchoglou... | lld:pubmed |
pubmed-article:10471587 | pubmed:author | pubmed-author:BatakiEE | lld:pubmed |
pubmed-article:10471587 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:10471587 | pubmed:volume | 43 | lld:pubmed |
pubmed-article:10471587 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:10471587 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:10471587 | pubmed:pagination | 2311-3 | lld:pubmed |
pubmed-article:10471587 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:10471587 | pubmed:meshHeading | pubmed-meshheading:10471587... | lld:pubmed |
pubmed-article:10471587 | pubmed:year | 1999 | lld:pubmed |
pubmed-article:10471587 | pubmed:articleTitle | Antimicrobial susceptibility testing of Chlamydia trachomatis using a reverse transcriptase PCR-based method. | lld:pubmed |
pubmed-article:10471587 | pubmed:affiliation | Division of Molecular and Genetic Medicine, University of Sheffield Medical School, Sheffield S10 2RX, United Kingdom. | lld:pubmed |
pubmed-article:10471587 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:10471587 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:10471587 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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