| pubmed-article:2444670 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:2444670 | lifeskim:mentions | umls-concept:C1265249 | lld:lifeskim |
| pubmed-article:2444670 | lifeskim:mentions | umls-concept:C0205147 | lld:lifeskim |
| pubmed-article:2444670 | lifeskim:mentions | umls-concept:C0035701 | lld:lifeskim |
| pubmed-article:2444670 | lifeskim:mentions | umls-concept:C0028952 | lld:lifeskim |
| pubmed-article:2444670 | lifeskim:mentions | umls-concept:C0439828 | lld:lifeskim |
| pubmed-article:2444670 | pubmed:issue | 7 | lld:pubmed |
| pubmed-article:2444670 | pubmed:dateCreated | 1987-12-17 | lld:pubmed |
| pubmed-article:2444670 | pubmed:abstractText | On the basis of information from computer-assisted sequence comparison of the Mycoplasma pneumoniae 16S ribosomal RNA (rRNA) sequences with sequences from various other mycoplasmal and bacterial species, we constructed M. pneumoniae-specific oligonucleotide probes complementary to variable regions in the 16S rRNA molecule. Using a DNA/RNA dot blot hybridization procedure, it was possible to detect less than 1 X 10(3) mycoplasmas. This test is a most sensitive assay for species-specific detection of bacteria. It can easily be adapted for detection and identification of other bacterial species and may have wide medical and industrial application. | lld:pubmed |
| pubmed-article:2444670 | pubmed:language | eng | lld:pubmed |
| pubmed-article:2444670 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:2444670 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:2444670 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:2444670 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:2444670 | pubmed:issn | 0022-1287 | lld:pubmed |
| pubmed-article:2444670 | pubmed:author | pubmed-author:StanbridgeE... | lld:pubmed |
| pubmed-article:2444670 | pubmed:author | pubmed-author:GöbelU BUB | lld:pubmed |
| pubmed-article:2444670 | pubmed:author | pubmed-author:GeiserAA | lld:pubmed |
| pubmed-article:2444670 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:2444670 | pubmed:volume | 133 | lld:pubmed |
| pubmed-article:2444670 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:2444670 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:2444670 | pubmed:pagination | 1969-74 | lld:pubmed |
| pubmed-article:2444670 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:2444670 | pubmed:meshHeading | pubmed-meshheading:2444670-... | lld:pubmed |
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| pubmed-article:2444670 | pubmed:meshHeading | pubmed-meshheading:2444670-... | lld:pubmed |
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| pubmed-article:2444670 | pubmed:meshHeading | pubmed-meshheading:2444670-... | lld:pubmed |
| pubmed-article:2444670 | pubmed:year | 1987 | lld:pubmed |
| pubmed-article:2444670 | pubmed:articleTitle | Oligonucleotide probes complementary to variable regions of ribosomal RNA discriminate between Mycoplasma species. | lld:pubmed |
| pubmed-article:2444670 | pubmed:affiliation | Institut für Medizinische Mikrobiologie und Hygiene, Klinikum der Universität Freiburg, FRG. | lld:pubmed |
| pubmed-article:2444670 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:2444670 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:2444670 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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