pubmed-article:18549897 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18549897 | lifeskim:mentions | umls-concept:C2239176 | lld:lifeskim |
pubmed-article:18549897 | lifeskim:mentions | umls-concept:C0069676 | lld:lifeskim |
pubmed-article:18549897 | lifeskim:mentions | umls-concept:C0017262 | lld:lifeskim |
pubmed-article:18549897 | lifeskim:mentions | umls-concept:C1881800 | lld:lifeskim |
pubmed-article:18549897 | lifeskim:mentions | umls-concept:C0752249 | lld:lifeskim |
pubmed-article:18549897 | lifeskim:mentions | umls-concept:C0443199 | lld:lifeskim |
pubmed-article:18549897 | lifeskim:mentions | umls-concept:C0851285 | lld:lifeskim |
pubmed-article:18549897 | lifeskim:mentions | umls-concept:C2911684 | lld:lifeskim |
pubmed-article:18549897 | lifeskim:mentions | umls-concept:C0185117 | lld:lifeskim |
pubmed-article:18549897 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:18549897 | pubmed:dateCreated | 2008-6-13 | lld:pubmed |
pubmed-article:18549897 | pubmed:abstractText | Osteopontin (OPN) is a potential therapeutic target in hepatocellular carcinoma (HCC), because it is a critical mediator of metastatic function. The molecular mechanisms that determine expression of OPN in HCC, however, are unknown. In this study, we examine differential OPN expression in the 2 HCC cell lines: HepG2 and Hep3B. | lld:pubmed |
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pubmed-article:18549897 | pubmed:language | eng | lld:pubmed |
pubmed-article:18549897 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18549897 | pubmed:citationSubset | AIM | lld:pubmed |
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pubmed-article:18549897 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18549897 | pubmed:month | Jun | lld:pubmed |
pubmed-article:18549897 | pubmed:issn | 1532-7361 | lld:pubmed |
pubmed-article:18549897 | pubmed:author | pubmed-author:KuoPaul CPC | lld:pubmed |
pubmed-article:18549897 | pubmed:author | pubmed-author:GuoHongtaoH | lld:pubmed |
pubmed-article:18549897 | pubmed:author | pubmed-author:EmaniSirishaS | lld:pubmed |
pubmed-article:18549897 | pubmed:author | pubmed-author:ZhangJinpingJ | lld:pubmed |
pubmed-article:18549897 | pubmed:author | pubmed-author:GuoLucieL | lld:pubmed |
pubmed-article:18549897 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:18549897 | pubmed:volume | 143 | lld:pubmed |
pubmed-article:18549897 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18549897 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18549897 | pubmed:pagination | 803-12 | lld:pubmed |
pubmed-article:18549897 | pubmed:dateRevised | 2011-8-1 | lld:pubmed |
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pubmed-article:18549897 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:18549897 | pubmed:articleTitle | RNA stability regulates differential expression of the metastasis protein, osteopontin, in hepatocellular cancer. | lld:pubmed |
pubmed-article:18549897 | pubmed:affiliation | Department of Surgery, Duke University Medical Center, Durham, NC 27710, USA. | lld:pubmed |
pubmed-article:18549897 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18549897 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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