| pubmed-article:21182784 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21182784 | lifeskim:mentions | umls-concept:C0042769 | lld:lifeskim |
| pubmed-article:21182784 | lifeskim:mentions | umls-concept:C0029347 | lld:lifeskim |
| pubmed-article:21182784 | lifeskim:mentions | umls-concept:C0012655 | lld:lifeskim |
| pubmed-article:21182784 | lifeskim:mentions | umls-concept:C0567416 | lld:lifeskim |
| pubmed-article:21182784 | lifeskim:mentions | umls-concept:C0065661 | lld:lifeskim |
| pubmed-article:21182784 | lifeskim:mentions | umls-concept:C0442805 | lld:lifeskim |
| pubmed-article:21182784 | lifeskim:mentions | umls-concept:C1518918 | lld:lifeskim |
| pubmed-article:21182784 | pubmed:dateCreated | 2011-1-17 | lld:pubmed |
| pubmed-article:21182784 | pubmed:abstractText | Mannose-binding lectin (MBL), a pattern recognition innate immune molecule, inhibits influenza A virus infection in vitro. MBL deficiency due to gene polymorphism in humans has been associated with infection susceptibility. These clinical observations were confirmed by animal model studies, in which mice genetically lacking MBL were susceptible to certain pathogens, including herpes simplex virus 2. | lld:pubmed |
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| pubmed-article:21182784 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:21182784 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:21182784 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21182784 | pubmed:issn | 1471-2172 | lld:pubmed |
| pubmed-article:21182784 | pubmed:author | pubmed-author:TakahashiKazu... | lld:pubmed |
| pubmed-article:21182784 | pubmed:author | pubmed-author:HartshornKeva... | lld:pubmed |
| pubmed-article:21182784 | pubmed:author | pubmed-author:WhiteMitchell... | lld:pubmed |
| pubmed-article:21182784 | pubmed:author | pubmed-author:ThielSteffenS | lld:pubmed |
| pubmed-article:21182784 | pubmed:author | pubmed-author:ChangWei-Chua... | lld:pubmed |
| pubmed-article:21182784 | pubmed:author | pubmed-author:MoyoPatienceP | lld:pubmed |
| pubmed-article:21182784 | pubmed:author | pubmed-author:McClearSheree... | lld:pubmed |
| pubmed-article:21182784 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21182784 | pubmed:volume | 11 | lld:pubmed |
| pubmed-article:21182784 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21182784 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21182784 | pubmed:pagination | 64 | lld:pubmed |
| pubmed-article:21182784 | pubmed:dateRevised | 2011-7-20 | lld:pubmed |
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| pubmed-article:21182784 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:21182784 | pubmed:articleTitle | Lack of the pattern recognition molecule mannose-binding lectin increases susceptibility to influenza A virus infection. | lld:pubmed |
| pubmed-article:21182784 | pubmed:affiliation | Department of Pediatrics, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA. | lld:pubmed |
| pubmed-article:21182784 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21182784 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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