pubmed-article:6224859 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:6224859 | lifeskim:mentions | umls-concept:C0010453 | lld:lifeskim |
pubmed-article:6224859 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
pubmed-article:6224859 | lifeskim:mentions | umls-concept:C0039194 | lld:lifeskim |
pubmed-article:6224859 | lifeskim:mentions | umls-concept:C0024534 | lld:lifeskim |
pubmed-article:6224859 | lifeskim:mentions | umls-concept:C0032149 | lld:lifeskim |
pubmed-article:6224859 | lifeskim:mentions | umls-concept:C0376518 | lld:lifeskim |
pubmed-article:6224859 | lifeskim:mentions | umls-concept:C1708528 | lld:lifeskim |
pubmed-article:6224859 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:6224859 | pubmed:dateCreated | 1983-10-8 | lld:pubmed |
pubmed-article:6224859 | pubmed:abstractText | Murine T cell populations specific for Plasmodium berghei parasites were generated in vitro from BALB/c immune lymph node cells. The malaria-specific T lymphocytes were shown: a) to proliferate specifically in vitro in response to stimulation with P. berghei-infected red blood cells; b) to exhibit the Thy-1+, Lyt-1+2- cell surface phenotype; c) to provide specific helper activity for an in vitro anti-hapten (TNP) plaque-forming cell antibody response; and d) to protect P. berghei-infected mice from early mortality due to cerebral malaria. | lld:pubmed |
pubmed-article:6224859 | pubmed:language | eng | lld:pubmed |
pubmed-article:6224859 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:6224859 | pubmed:citationSubset | AIM | lld:pubmed |
pubmed-article:6224859 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:6224859 | pubmed:month | Sep | lld:pubmed |
pubmed-article:6224859 | pubmed:issn | 0022-1767 | lld:pubmed |
pubmed-article:6224859 | pubmed:author | pubmed-author:LambertP HPH | lld:pubmed |
pubmed-article:6224859 | pubmed:author | pubmed-author:MONTIVV | lld:pubmed |
pubmed-article:6224859 | pubmed:author | pubmed-author:EngersH DHD | lld:pubmed |
pubmed-article:6224859 | pubmed:author | pubmed-author:WeintraubJJ | lld:pubmed |
pubmed-article:6224859 | pubmed:author | pubmed-author:ZublerRR | lld:pubmed |
pubmed-article:6224859 | pubmed:author | pubmed-author:FinleyRR | lld:pubmed |
pubmed-article:6224859 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:6224859 | pubmed:volume | 131 | lld:pubmed |
pubmed-article:6224859 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:6224859 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:6224859 | pubmed:pagination | 1522-6 | lld:pubmed |
pubmed-article:6224859 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
pubmed-article:6224859 | pubmed:meshHeading | pubmed-meshheading:6224859-... | lld:pubmed |
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pubmed-article:6224859 | pubmed:meshHeading | pubmed-meshheading:6224859-... | lld:pubmed |
pubmed-article:6224859 | pubmed:year | 1983 | lld:pubmed |
pubmed-article:6224859 | pubmed:articleTitle | Prevention of cerebral malaria by adoptive transfer of malaria-specific cultured T cells into mice infected with Plasmodium berghei. | lld:pubmed |
pubmed-article:6224859 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:6224859 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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