pubmed-article:19223492 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19223492 | lifeskim:mentions | umls-concept:C0598934 | lld:lifeskim |
pubmed-article:19223492 | lifeskim:mentions | umls-concept:C0220918 | lld:lifeskim |
pubmed-article:19223492 | lifeskim:mentions | umls-concept:C1546857 | lld:lifeskim |
pubmed-article:19223492 | lifeskim:mentions | umls-concept:C1515655 | lld:lifeskim |
pubmed-article:19223492 | lifeskim:mentions | umls-concept:C1312550 | lld:lifeskim |
pubmed-article:19223492 | lifeskim:mentions | umls-concept:C0301625 | lld:lifeskim |
pubmed-article:19223492 | pubmed:issue | 5 | lld:pubmed |
pubmed-article:19223492 | pubmed:dateCreated | 2009-3-2 | lld:pubmed |
pubmed-article:19223492 | pubmed:abstractText | Vitamin E analogues are potent novel anticancer drugs. The purpose of this study was to elucidate the cellular target by which these agents, represented by alpha-tocopoheryl succinate (alpha-TOS), suppress tumors in vivo, with the focus on the mitochondrial complex II (CII). | lld:pubmed |
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pubmed-article:19223492 | pubmed:language | eng | lld:pubmed |
pubmed-article:19223492 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19223492 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:19223492 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19223492 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:19223492 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19223492 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:19223492 | pubmed:month | Mar | lld:pubmed |
pubmed-article:19223492 | pubmed:issn | 1078-0432 | lld:pubmed |
pubmed-article:19223492 | pubmed:author | pubmed-author:NeuzilJiriJ | lld:pubmed |
pubmed-article:19223492 | pubmed:author | pubmed-author:BrunkUlf TUT | lld:pubmed |
pubmed-article:19223492 | pubmed:author | pubmed-author:FreemanRuthR | lld:pubmed |
pubmed-article:19223492 | pubmed:author | pubmed-author:RalphStephen... | lld:pubmed |
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pubmed-article:19223492 | pubmed:author | pubmed-author:RohlenaJakubJ | lld:pubmed |
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pubmed-article:19223492 | pubmed:author | pubmed-author:ValisKarelK | lld:pubmed |
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pubmed-article:19223492 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:19223492 | pubmed:day | 1 | lld:pubmed |
pubmed-article:19223492 | pubmed:volume | 15 | lld:pubmed |
pubmed-article:19223492 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:19223492 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:19223492 | pubmed:pagination | 1593-600 | lld:pubmed |
pubmed-article:19223492 | pubmed:dateRevised | 2011-4-28 | lld:pubmed |
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pubmed-article:19223492 | pubmed:year | 2009 | lld:pubmed |
pubmed-article:19223492 | pubmed:articleTitle | Suppression of tumor growth in vivo by the mitocan alpha-tocopheryl succinate requires respiratory complex II. | lld:pubmed |
pubmed-article:19223492 | pubmed:affiliation | Apoptosis Research Group and Genomic Research Centre, School of Medical Science, Griffith University, Southport, Queensland, Australia. l.dong@griffith.edu.au | lld:pubmed |
pubmed-article:19223492 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:19223492 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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