| pubmed-article:7637023 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:7637023 | lifeskim:mentions | umls-concept:C0042776 | lld:lifeskim |
| pubmed-article:7637023 | lifeskim:mentions | umls-concept:C0016514 | lld:lifeskim |
| pubmed-article:7637023 | lifeskim:mentions | umls-concept:C0007452 | lld:lifeskim |
| pubmed-article:7637023 | lifeskim:mentions | umls-concept:C0597358 | lld:lifeskim |
| pubmed-article:7637023 | pubmed:issue | 9 | lld:pubmed |
| pubmed-article:7637023 | pubmed:dateCreated | 1995-9-14 | lld:pubmed |
| pubmed-article:7637023 | pubmed:abstractText | Binding of foot-and-mouth disease virus (FMDV) to cells requires an arginine-glycine-aspartic acid (RGD) sequence in the capsid protein VP1. We have genetically engineered an FMDV in which these three amino acids have been deleted, producing a virus particle which is unable to bind to cells. Cattle vaccinated with these receptor binding site-deleted virions were protected from disease when challenged with a virulent virus, demonstrating that these RGD-deleted viruses could serve as the basis for foot-and-mouth disease vaccines safer than those currently in use. This strategy may prove useful in the development of vaccines for other viral diseases. | lld:pubmed |
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| pubmed-article:7637023 | pubmed:language | eng | lld:pubmed |
| pubmed-article:7637023 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:7637023 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:7637023 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:7637023 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:7637023 | pubmed:issn | 0022-538X | lld:pubmed |
| pubmed-article:7637023 | pubmed:author | pubmed-author:BaxtBB | lld:pubmed |
| pubmed-article:7637023 | pubmed:author | pubmed-author:MasonP WPW | lld:pubmed |
| pubmed-article:7637023 | pubmed:author | pubmed-author:LubrothJJ | lld:pubmed |
| pubmed-article:7637023 | pubmed:author | pubmed-author:RiederEE | lld:pubmed |
| pubmed-article:7637023 | pubmed:author | pubmed-author:McKennaT STS | lld:pubmed |
| pubmed-article:7637023 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:7637023 | pubmed:volume | 69 | lld:pubmed |
| pubmed-article:7637023 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:7637023 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:7637023 | pubmed:pagination | 5787-90 | lld:pubmed |
| pubmed-article:7637023 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:7637023 | pubmed:year | 1995 | lld:pubmed |
| pubmed-article:7637023 | pubmed:articleTitle | Receptor binding site-deleted foot-and-mouth disease (FMD) virus protects cattle from FMD. | lld:pubmed |
| pubmed-article:7637023 | pubmed:affiliation | Plum Island Animal Disease Center, U.S. Department of Agriculture, Greenport, New York 11944, USA. | lld:pubmed |
| pubmed-article:7637023 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:7637023 | pubmed:publicationType | Comparative Study | lld:pubmed |
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