pubmed-article:170223 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:170223 | lifeskim:mentions | umls-concept:C0019351 | lld:lifeskim |
pubmed-article:170223 | lifeskim:mentions | umls-concept:C0021311 | lld:lifeskim |
pubmed-article:170223 | lifeskim:mentions | umls-concept:C0007634 | lld:lifeskim |
pubmed-article:170223 | lifeskim:mentions | umls-concept:C0025914 | lld:lifeskim |
pubmed-article:170223 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
pubmed-article:170223 | lifeskim:mentions | umls-concept:C1510411 | lld:lifeskim |
pubmed-article:170223 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:170223 | pubmed:dateCreated | 1976-1-2 | lld:pubmed |
pubmed-article:170223 | pubmed:abstractText | A transformed mouse cell line (H238) was obtained following the infection of 238 mouse cells with ultraviolet (UV) irradiation-inactivated herpes simplex virus type 2 (HSV-2). The transformed cells produced tumors with a 100% incidence within 8 weeks in 6-week-old syngeneic BALB/c mice at an inoculum of 1 times 10(6). Indirect immunofluorescence (IF) tests revealed the presence of HSV antigens in the transformed cells. Antibodies to HSV-2 were found in the sera of tumor-bearing animals by neutralization and IF techniques. Neither HSV-2 infectious virus nor viral antigens could be detected by the transfer of transformed-cell DNA into permissive cells. | lld:pubmed |
pubmed-article:170223 | pubmed:language | eng | lld:pubmed |
pubmed-article:170223 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:170223 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:170223 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:170223 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:170223 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:170223 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:170223 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:170223 | pubmed:month | Oct | lld:pubmed |
pubmed-article:170223 | pubmed:issn | 0020-7136 | lld:pubmed |
pubmed-article:170223 | pubmed:author | pubmed-author:OrmeT WTW | lld:pubmed |
pubmed-article:170223 | pubmed:author | pubmed-author:BoydA LAL | lld:pubmed |
pubmed-article:170223 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:170223 | pubmed:day | 15 | lld:pubmed |
pubmed-article:170223 | pubmed:volume | 16 | lld:pubmed |
pubmed-article:170223 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:170223 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:170223 | pubmed:pagination | 526-38 | lld:pubmed |
pubmed-article:170223 | pubmed:dateRevised | 2007-7-24 | lld:pubmed |
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pubmed-article:170223 | pubmed:meshHeading | pubmed-meshheading:170223-T... | lld:pubmed |
pubmed-article:170223 | pubmed:year | 1975 | lld:pubmed |
pubmed-article:170223 | pubmed:articleTitle | Transformation of mouse cells after infection with ultraviolet irradiation-inactivated herpes simplex virus type 2. | lld:pubmed |
pubmed-article:170223 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:170223 | pubmed:publicationType | In Vitro | lld:pubmed |
pubmed-article:170223 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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