| pubmed-article:19259792 | rdf:type | pubmed:Citation | lld:pubmed |
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| pubmed-article:19259792 | lifeskim:mentions | umls-concept:C0567416 | lld:lifeskim |
| pubmed-article:19259792 | lifeskim:mentions | umls-concept:C0003241 | lld:lifeskim |
| pubmed-article:19259792 | lifeskim:mentions | umls-concept:C0085379 | lld:lifeskim |
| pubmed-article:19259792 | lifeskim:mentions | umls-concept:C0599894 | lld:lifeskim |
| pubmed-article:19259792 | lifeskim:mentions | umls-concept:C0442335 | lld:lifeskim |
| pubmed-article:19259792 | pubmed:issue | 6 | lld:pubmed |
| pubmed-article:19259792 | pubmed:dateCreated | 2009-5-6 | lld:pubmed |
| pubmed-article:19259792 | pubmed:abstractText | The purpose of this study was to investigate the potential of a T-cell-related targeting method using a lentiviral vector-based gene delivery system. | lld:pubmed |
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| pubmed-article:19259792 | pubmed:language | eng | lld:pubmed |
| pubmed-article:19259792 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19259792 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:19259792 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19259792 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:19259792 | pubmed:issn | 1573-904X | lld:pubmed |
| pubmed-article:19259792 | pubmed:author | pubmed-author:WangPinP | lld:pubmed |
| pubmed-article:19259792 | pubmed:author | pubmed-author:JooKye-IlKI | lld:pubmed |
| pubmed-article:19259792 | pubmed:author | pubmed-author:YangHaiguangH | lld:pubmed |
| pubmed-article:19259792 | pubmed:author | pubmed-author:ZieglerLeslie... | lld:pubmed |
| pubmed-article:19259792 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19259792 | pubmed:volume | 26 | lld:pubmed |
| pubmed-article:19259792 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19259792 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19259792 | pubmed:pagination | 1432-45 | lld:pubmed |
| pubmed-article:19259792 | pubmed:dateRevised | 2011-9-26 | lld:pubmed |
| pubmed-article:19259792 | pubmed:meshHeading | pubmed-meshheading:19259792... | lld:pubmed |
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| pubmed-article:19259792 | pubmed:meshHeading | pubmed-meshheading:19259792... | lld:pubmed |
| pubmed-article:19259792 | pubmed:meshHeading | pubmed-meshheading:19259792... | lld:pubmed |
| pubmed-article:19259792 | pubmed:meshHeading | pubmed-meshheading:19259792... | lld:pubmed |
| pubmed-article:19259792 | pubmed:meshHeading | pubmed-meshheading:19259792... | lld:pubmed |
| pubmed-article:19259792 | pubmed:meshHeading | pubmed-meshheading:19259792... | lld:pubmed |
| pubmed-article:19259792 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19259792 | pubmed:articleTitle | Cell type-specific targeting with surface-engineered lentiviral vectors co-displaying OKT3 antibody and fusogenic molecule. | lld:pubmed |
| pubmed-article:19259792 | pubmed:affiliation | Mork Family Department of Chemical Engineering and Materials Science, University of Southern California, 925 Bloom Walk, Los Angeles, CA 90089, USA. | lld:pubmed |
| pubmed-article:19259792 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:19259792 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
