pubmed-article:6693193 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:6693193 | lifeskim:mentions | umls-concept:C0007634 | lld:lifeskim |
pubmed-article:6693193 | lifeskim:mentions | umls-concept:C0016055 | lld:lifeskim |
pubmed-article:6693193 | lifeskim:mentions | umls-concept:C0008018 | lld:lifeskim |
pubmed-article:6693193 | lifeskim:mentions | umls-concept:C0439536 | lld:lifeskim |
pubmed-article:6693193 | lifeskim:mentions | umls-concept:C2349975 | lld:lifeskim |
pubmed-article:6693193 | lifeskim:mentions | umls-concept:C1519667 | lld:lifeskim |
pubmed-article:6693193 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:6693193 | pubmed:dateCreated | 1984-3-15 | lld:pubmed |
pubmed-article:6693193 | pubmed:abstractText | SV40 transformants of human embryo fibroblasts showed an enhanced chemotactic response to fibronectin and conditioned medium of fibroblasts in comparison to the non-transformed cells. An even higher chemotactic response was characteristic for a malignant human fibrosarcoma cell line, whereas cells derived from low-grade malignant dermatofibrosarcoma showed a normal response in the Boyden chamber assay. The high stimulation of chemotaxis is paralleled by a reduced synthesis and an altered deposition of fibronectin in the pericellular matrix of these cells. Both high chemotactic response and lack of deposition of fibronectin may play a role in tissue invasion and formation of metastasis by malignant tumors. | lld:pubmed |
pubmed-article:6693193 | pubmed:language | eng | lld:pubmed |
pubmed-article:6693193 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:6693193 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:6693193 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:6693193 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:6693193 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:6693193 | pubmed:month | Jan | lld:pubmed |
pubmed-article:6693193 | pubmed:issn | 0020-7136 | lld:pubmed |
pubmed-article:6693193 | pubmed:author | pubmed-author:KriegTT | lld:pubmed |
pubmed-article:6693193 | pubmed:author | pubmed-author:MüllerP KPK | lld:pubmed |
pubmed-article:6693193 | pubmed:author | pubmed-author:AlbiniAA | lld:pubmed |
pubmed-article:6693193 | pubmed:author | pubmed-author:MensingHH | lld:pubmed |
pubmed-article:6693193 | pubmed:author | pubmed-author:PontzB FBF | lld:pubmed |
pubmed-article:6693193 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:6693193 | pubmed:day | 15 | lld:pubmed |
pubmed-article:6693193 | pubmed:volume | 33 | lld:pubmed |
pubmed-article:6693193 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:6693193 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:6693193 | pubmed:pagination | 43-8 | lld:pubmed |
pubmed-article:6693193 | pubmed:dateRevised | 2007-7-24 | lld:pubmed |
pubmed-article:6693193 | pubmed:meshHeading | pubmed-meshheading:6693193-... | lld:pubmed |
pubmed-article:6693193 | pubmed:meshHeading | pubmed-meshheading:6693193-... | lld:pubmed |
pubmed-article:6693193 | pubmed:meshHeading | pubmed-meshheading:6693193-... | lld:pubmed |
pubmed-article:6693193 | pubmed:meshHeading | pubmed-meshheading:6693193-... | lld:pubmed |
pubmed-article:6693193 | pubmed:meshHeading | pubmed-meshheading:6693193-... | lld:pubmed |
pubmed-article:6693193 | pubmed:meshHeading | pubmed-meshheading:6693193-... | lld:pubmed |
pubmed-article:6693193 | pubmed:meshHeading | pubmed-meshheading:6693193-... | lld:pubmed |
pubmed-article:6693193 | pubmed:meshHeading | pubmed-meshheading:6693193-... | lld:pubmed |
pubmed-article:6693193 | pubmed:year | 1984 | lld:pubmed |
pubmed-article:6693193 | pubmed:articleTitle | Enhanced chemotaxis of tumor-derived and virus-transformed cells to fibronectin and fibroblast-conditioned medium. | lld:pubmed |
pubmed-article:6693193 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:6693193 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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