| pubmed-article:17897458 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17897458 | lifeskim:mentions | umls-concept:C0003316 | lld:lifeskim |
| pubmed-article:17897458 | lifeskim:mentions | umls-concept:C0042210 | lld:lifeskim |
| pubmed-article:17897458 | lifeskim:mentions | umls-concept:C0348026 | lld:lifeskim |
| pubmed-article:17897458 | lifeskim:mentions | umls-concept:C1527148 | lld:lifeskim |
| pubmed-article:17897458 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
| pubmed-article:17897458 | lifeskim:mentions | umls-concept:C0336791 | lld:lifeskim |
| pubmed-article:17897458 | lifeskim:mentions | umls-concept:C1707689 | lld:lifeskim |
| pubmed-article:17897458 | pubmed:dateCreated | 2008-2-7 | lld:pubmed |
| pubmed-article:17897458 | pubmed:abstractText | In an epitope-based vaccine setting, the use of conserved epitopes would be expected to provide broader protection across multiple strains, or even species, than epitopes derived from highly variable genome regions. Conversely, in a diagnostic and disease monitoring setting, epitopes that are specific to a given pathogen strain, for example, can be used to monitor responses to that particular infectious strain. In both cases, concrete information pertaining to the degree of conservancy of the epitope(s) considered is crucial. | lld:pubmed |
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| pubmed-article:17897458 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:17897458 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:17897458 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17897458 | pubmed:issn | 1471-2105 | lld:pubmed |
| pubmed-article:17897458 | pubmed:author | pubmed-author:FuY PYP | lld:pubmed |
| pubmed-article:17897458 | pubmed:author | pubmed-author:SetteAlessand... | lld:pubmed |
| pubmed-article:17897458 | pubmed:author | pubmed-author:SidneyJohnJ | lld:pubmed |
| pubmed-article:17897458 | pubmed:author | pubmed-author:BuiHuynh-HoaH... | lld:pubmed |
| pubmed-article:17897458 | pubmed:author | pubmed-author:FussederNicol... | lld:pubmed |
| pubmed-article:17897458 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:17897458 | pubmed:volume | 8 | lld:pubmed |
| pubmed-article:17897458 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17897458 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17897458 | pubmed:pagination | 361 | lld:pubmed |
| pubmed-article:17897458 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:17897458 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17897458 | pubmed:articleTitle | Development of an epitope conservancy analysis tool to facilitate the design of epitope-based diagnostics and vaccines. | lld:pubmed |
| pubmed-article:17897458 | pubmed:affiliation | La Jolla Institute for Allergy and Immunology, Division of Vaccine Discovery, 9420 Athena Circle, La Jolla, CA 92037, USA. hbui@isisph.com | lld:pubmed |
| pubmed-article:17897458 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17897458 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:17897458 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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