pubmed-article:10802169 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:10802169 | lifeskim:mentions | umls-concept:C0038409 | lld:lifeskim |
pubmed-article:10802169 | lifeskim:mentions | umls-concept:C0033621 | lld:lifeskim |
pubmed-article:10802169 | lifeskim:mentions | umls-concept:C0596988 | lld:lifeskim |
pubmed-article:10802169 | lifeskim:mentions | umls-concept:C0332597 | lld:lifeskim |
pubmed-article:10802169 | lifeskim:mentions | umls-concept:C0017362 | lld:lifeskim |
pubmed-article:10802169 | lifeskim:mentions | umls-concept:C1413745 | lld:lifeskim |
pubmed-article:10802169 | lifeskim:mentions | umls-concept:C1527177 | lld:lifeskim |
pubmed-article:10802169 | lifeskim:mentions | umls-concept:C0441513 | lld:lifeskim |
pubmed-article:10802169 | lifeskim:mentions | umls-concept:C0728938 | lld:lifeskim |
pubmed-article:10802169 | lifeskim:mentions | umls-concept:C1515655 | lld:lifeskim |
pubmed-article:10802169 | lifeskim:mentions | umls-concept:C0061365 | lld:lifeskim |
pubmed-article:10802169 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:10802169 | pubmed:dateCreated | 2000-7-11 | lld:pubmed |
pubmed-article:10802169 | pubmed:abstractText | The gbpC gene encoding the glucan-binding protein C which is involved in dextran (glucan)-dependent aggregation (ddag) of Streptococcus mutans has been identified by random mutagenesis. We analyzed ddag(-) mutants containing the intact gbpC gene and found that these mutants possessed a large and characteristic duplication of a region of the chromosome which was responsible for the phenotype. Based upon characterization of these duplications, we developed a strategy to introduce a duplication into any specific region of the chromosome of these organisms. The 690-bp gene responsible for the ddag(-) phenotype was identified within a 60-kb region by observing ddag (positive or negative) phenotypes of successively constructed specific duplication mutants. | lld:pubmed |
pubmed-article:10802169 | pubmed:language | eng | lld:pubmed |
pubmed-article:10802169 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10802169 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:10802169 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10802169 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10802169 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10802169 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10802169 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10802169 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:10802169 | pubmed:month | May | lld:pubmed |
pubmed-article:10802169 | pubmed:issn | 0378-1097 | lld:pubmed |
pubmed-article:10802169 | pubmed:author | pubmed-author:SatoYY | lld:pubmed |
pubmed-article:10802169 | pubmed:author | pubmed-author:YamamotoYY | lld:pubmed |
pubmed-article:10802169 | pubmed:author | pubmed-author:KizakiHH | lld:pubmed |
pubmed-article:10802169 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:10802169 | pubmed:day | 15 | lld:pubmed |
pubmed-article:10802169 | pubmed:volume | 186 | lld:pubmed |
pubmed-article:10802169 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:10802169 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:10802169 | pubmed:pagination | 187-91 | lld:pubmed |
pubmed-article:10802169 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
pubmed-article:10802169 | pubmed:meshHeading | pubmed-meshheading:10802169... | lld:pubmed |
pubmed-article:10802169 | pubmed:meshHeading | pubmed-meshheading:10802169... | lld:pubmed |
pubmed-article:10802169 | pubmed:meshHeading | pubmed-meshheading:10802169... | lld:pubmed |
pubmed-article:10802169 | pubmed:meshHeading | pubmed-meshheading:10802169... | lld:pubmed |
pubmed-article:10802169 | pubmed:meshHeading | pubmed-meshheading:10802169... | lld:pubmed |
pubmed-article:10802169 | pubmed:meshHeading | pubmed-meshheading:10802169... | lld:pubmed |
pubmed-article:10802169 | pubmed:meshHeading | pubmed-meshheading:10802169... | lld:pubmed |
pubmed-article:10802169 | pubmed:meshHeading | pubmed-meshheading:10802169... | lld:pubmed |
pubmed-article:10802169 | pubmed:meshHeading | pubmed-meshheading:10802169... | lld:pubmed |
pubmed-article:10802169 | pubmed:meshHeading | pubmed-meshheading:10802169... | lld:pubmed |
pubmed-article:10802169 | pubmed:meshHeading | pubmed-meshheading:10802169... | lld:pubmed |
pubmed-article:10802169 | pubmed:year | 2000 | lld:pubmed |
pubmed-article:10802169 | pubmed:articleTitle | Construction of region-specific partial duplication mutants (merodiploid mutants) to identify the regulatory gene for the glucan-binding protein C gene in vivo in Streptococcus mutans. | lld:pubmed |
pubmed-article:10802169 | pubmed:affiliation | Oral Health Science Center, Tokyo Dental College, 2-2, Masago 1-chome, Mihama-ku, Chiba City, Japan. yusato@tdc.ac.jp | lld:pubmed |
pubmed-article:10802169 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:10802169 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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