| pubmed-article:21203416 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21203416 | lifeskim:mentions | umls-concept:C0085478 | lld:lifeskim |
| pubmed-article:21203416 | lifeskim:mentions | umls-concept:C0024432 | lld:lifeskim |
| pubmed-article:21203416 | lifeskim:mentions | umls-concept:C0151317 | lld:lifeskim |
| pubmed-article:21203416 | lifeskim:mentions | umls-concept:C0332157 | lld:lifeskim |
| pubmed-article:21203416 | lifeskim:mentions | umls-concept:C0205178 | lld:lifeskim |
| pubmed-article:21203416 | lifeskim:mentions | umls-concept:C1140694 | lld:lifeskim |
| pubmed-article:21203416 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
| pubmed-article:21203416 | pubmed:issue | 12 | lld:pubmed |
| pubmed-article:21203416 | pubmed:dateCreated | 2011-1-4 | lld:pubmed |
| pubmed-article:21203416 | pubmed:abstractText | Periodontitis is the most common human infection affecting tooth-supporting structures. It was shown to play a role in aggravating atherosclerosis. To deepen our understanding of the pathogenesis of this disease, we exposed human macrophages to an oral bacteria, Porphyromonas gingivalis (P. gingivalis), either as live bacteria or its LPS or fimbria. Microarray data from treated macrophages or control cells were analyzed to define molecular signatures. Changes in genes identified in relevant pathways were validated by RT-PCR. | lld:pubmed |
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| pubmed-article:21203416 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:21203416 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:21203416 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21203416 | pubmed:issn | 1932-6203 | lld:pubmed |
| pubmed-article:21203416 | pubmed:author | pubmed-author:YowMM | lld:pubmed |
| pubmed-article:21203416 | pubmed:author | pubmed-author:AmarSalomonS | lld:pubmed |
| pubmed-article:21203416 | pubmed:author | pubmed-author:ZhouQingdeQ | lld:pubmed |
| pubmed-article:21203416 | pubmed:author | pubmed-author:HuHanH | lld:pubmed |
| pubmed-article:21203416 | pubmed:author | pubmed-author:YuWen-HanWH | lld:pubmed |
| pubmed-article:21203416 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21203416 | pubmed:volume | 5 | lld:pubmed |
| pubmed-article:21203416 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21203416 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21203416 | pubmed:pagination | e15613 | lld:pubmed |
| pubmed-article:21203416 | pubmed:dateRevised | 2011-7-20 | lld:pubmed |
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| pubmed-article:21203416 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:21203416 | pubmed:articleTitle | Bioinformatics analysis of macrophages exposed to Porphyromonas gingivalis: implications in acute vs. chronic infections. | lld:pubmed |
| pubmed-article:21203416 | pubmed:affiliation | Bioinformatics Graduate Program, Boston University, Boston, Massachusetts, United States of America. | lld:pubmed |
| pubmed-article:21203416 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21203416 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
