| pubmed-article:21569301 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21569301 | lifeskim:mentions | umls-concept:C0019682 | lld:lifeskim |
| pubmed-article:21569301 | lifeskim:mentions | umls-concept:C0598312 | lld:lifeskim |
| pubmed-article:21569301 | lifeskim:mentions | umls-concept:C1412181 | lld:lifeskim |
| pubmed-article:21569301 | lifeskim:mentions | umls-concept:C1705810 | lld:lifeskim |
| pubmed-article:21569301 | pubmed:dateCreated | 2011-6-20 | lld:pubmed |
| pubmed-article:21569301 | pubmed:abstractText | Gene trap insertional mutagenesis was used as a high-throughput approach to discover cellular genes participating in viral infection by screening libraries of cells selected for survival from lytic infection with a variety of viruses. Cells harboring a disrupted ADAM10 (A Disintegrin and Metalloprotease 10) allele survived reovirus infection, and subsequently ADAM10 was shown by RNA interference to be important for replication of HIV-1. | lld:pubmed |
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| pubmed-article:21569301 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21569301 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21569301 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:21569301 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21569301 | pubmed:issn | 1742-4690 | lld:pubmed |
| pubmed-article:21569301 | pubmed:author | pubmed-author:YuGuangliG | lld:pubmed |
