pubmed-article:10637601 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:10637601 | lifeskim:mentions | umls-concept:C0242643 | lld:lifeskim |
pubmed-article:10637601 | lifeskim:mentions | umls-concept:C0596902 | lld:lifeskim |
pubmed-article:10637601 | lifeskim:mentions | umls-concept:C0542341 | lld:lifeskim |
pubmed-article:10637601 | lifeskim:mentions | umls-concept:C0439064 | lld:lifeskim |
pubmed-article:10637601 | lifeskim:mentions | umls-concept:C0205463 | lld:lifeskim |
pubmed-article:10637601 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:10637601 | pubmed:dateCreated | 2000-3-2 | lld:pubmed |
pubmed-article:10637601 | pubmed:abstractText | Multidrug resistance mediated by the drug-efflux protein P-glycoprotein (P-gp) is one mechanism that tumor cells use to escape death induced by chemotherapeutic drugs. Although it is irrefutable that P-gp can efflux xenobiotics out of cells, biological regulatory functions for P-gp in multicellular organisms have yet to be established firmly. Recent observations have challenged the notion that P-gp has evolved merely to efflux xenotoxins out of healthy cells and raised the possibility that P-gp and related transporter molecules might play a fundamental role in regulating cell differentiation, proliferation and survival. | lld:pubmed |
pubmed-article:10637601 | pubmed:language | eng | lld:pubmed |
pubmed-article:10637601 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10637601 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:10637601 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10637601 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10637601 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:10637601 | pubmed:month | Jan | lld:pubmed |
pubmed-article:10637601 | pubmed:issn | 0968-0004 | lld:pubmed |
pubmed-article:10637601 | pubmed:author | pubmed-author:SmythM JMJ | lld:pubmed |
pubmed-article:10637601 | pubmed:author | pubmed-author:JohnstoneR... | lld:pubmed |
pubmed-article:10637601 | pubmed:author | pubmed-author:RuefliA AAA | lld:pubmed |
pubmed-article:10637601 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:10637601 | pubmed:volume | 25 | lld:pubmed |
pubmed-article:10637601 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:10637601 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:10637601 | pubmed:pagination | 1-6 | lld:pubmed |
pubmed-article:10637601 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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pubmed-article:10637601 | pubmed:meshHeading | pubmed-meshheading:10637601... | lld:pubmed |
pubmed-article:10637601 | pubmed:year | 2000 | lld:pubmed |
pubmed-article:10637601 | pubmed:articleTitle | Multiple physiological functions for multidrug transporter P-glycoprotein? | lld:pubmed |
pubmed-article:10637601 | pubmed:affiliation | Cellular Cytotoxicity Laboratory, The Austin Research Institute, Austin Hospital, Studley Road, Heidelberg 3084, Victoria, Australia. r.johnstone@ari.unimelb.edu.au | lld:pubmed |
pubmed-article:10637601 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:10637601 | pubmed:publicationType | Review | lld:pubmed |
pubmed-article:10637601 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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