| pubmed-article:3753613 | rdf:type | pubmed:Citation | lld:pubmed |
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| pubmed-article:3753613 | lifeskim:mentions | umls-concept:C0007634 | lld:lifeskim |
| pubmed-article:3753613 | lifeskim:mentions | umls-concept:C0033147 | lld:lifeskim |
| pubmed-article:3753613 | lifeskim:mentions | umls-concept:C0033684 | lld:lifeskim |
| pubmed-article:3753613 | lifeskim:mentions | umls-concept:C0205245 | lld:lifeskim |
| pubmed-article:3753613 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
| pubmed-article:3753613 | lifeskim:mentions | umls-concept:C0751608 | lld:lifeskim |
| pubmed-article:3753613 | lifeskim:mentions | umls-concept:C1704222 | lld:lifeskim |
| pubmed-article:3753613 | lifeskim:mentions | umls-concept:C2911684 | lld:lifeskim |
| pubmed-article:3753613 | lifeskim:mentions | umls-concept:C0185117 | lld:lifeskim |
| pubmed-article:3753613 | pubmed:issue | 1 | lld:pubmed |
| pubmed-article:3753613 | pubmed:dateCreated | 1986-1-24 | lld:pubmed |
| pubmed-article:3753613 | pubmed:abstractText | A cDNA library designed for high-level expression of measles virus-specific gene products in mammalian cells was generated. From this library, functional clones which contained the entire protein-coding sequences of the nucleocapsid (N) and the phosphoprotein (P) genes were isolated. By DNA-mediated gene transfer into a line of simian virus 40-transformed monkey kidney cells, the N-specific cDNA was expressed into a single polypeptide of about 60,000 Mr, which was immunoprecipitated by monoclonal antibodies against the measles virus N protein. In contrast, the P-specific cDNA could be expressed into either one or two species of polypeptides of 75,000 or 70,000 Mr, both of which were immunoprecipitated by monoclonal antibodies against the measles virus P protein. | lld:pubmed |
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| pubmed-article:3753613 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:3753613 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:3753613 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:3753613 | pubmed:month | Jan | lld:pubmed |
| pubmed-article:3753613 | pubmed:issn | 0022-538X | lld:pubmed |
| pubmed-article:3753613 | pubmed:author | pubmed-author:HiranoAA | lld:pubmed |
| pubmed-article:3753613 | pubmed:author | pubmed-author:WongT CTC | lld:pubmed |
| pubmed-article:3753613 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:3753613 | pubmed:volume | 57 | lld:pubmed |
| pubmed-article:3753613 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:3753613 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:3753613 | pubmed:pagination | 343-8 | lld:pubmed |
| pubmed-article:3753613 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:3753613 | pubmed:year | 1986 | lld:pubmed |
| pubmed-article:3753613 | pubmed:articleTitle | Functional cDNA library for efficient expression of measles virus-specific gene products in primate cells. | lld:pubmed |
| pubmed-article:3753613 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:3753613 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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