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| pubmed-article:12011119 | lifeskim:mentions | umls-concept:C0042172 | lld:lifeskim |
| pubmed-article:12011119 | lifeskim:mentions | umls-concept:C1449575 | lld:lifeskim |
| pubmed-article:12011119 | lifeskim:mentions | umls-concept:C0220825 | lld:lifeskim |
| pubmed-article:12011119 | lifeskim:mentions | umls-concept:C1704259 | lld:lifeskim |
| pubmed-article:12011119 | lifeskim:mentions | umls-concept:C1519522 | lld:lifeskim |
| pubmed-article:12011119 | lifeskim:mentions | umls-concept:C1705987 | lld:lifeskim |
| pubmed-article:12011119 | lifeskim:mentions | umls-concept:C0237881 | lld:lifeskim |
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| pubmed-article:12011119 | lifeskim:mentions | umls-concept:C0750502 | lld:lifeskim |
| pubmed-article:12011119 | pubmed:issue | 10 | lld:pubmed |
| pubmed-article:12011119 | pubmed:dateCreated | 2002-5-15 | lld:pubmed |
| pubmed-article:12011119 | pubmed:abstractText | E-cadherin (E-cad) and its associated intracellular molecules, catenins, are critical for intercellular epithelial adhesion and are often expressed in non-small-cell lung carcinomas (NSCLCs). We constructed tissue microarrays (TMAs) to investigate the expression of cadherins and catenins and their prognostic significance in NSCLC. | lld:pubmed |
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| pubmed-article:12011119 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:12011119 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:12011119 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:12011119 | pubmed:month | May | lld:pubmed |
| pubmed-article:12011119 | pubmed:issn | 0732-183X | lld:pubmed |
| pubmed-article:12011119 | pubmed:author | pubmed-author:FranklinW AWA | lld:pubmed |
| pubmed-article:12011119 | pubmed:author | pubmed-author:BaronAA | lld:pubmed |
| pubmed-article:12011119 | pubmed:author | pubmed-author:HirschF RFR | lld:pubmed |
| pubmed-article:12011119 | pubmed:author | pubmed-author:GemmillR MRM | lld:pubmed |
| pubmed-article:12011119 | pubmed:author | pubmed-author:DrabkinH AHA | lld:pubmed |
| pubmed-article:12011119 | pubmed:author | pubmed-author:BremnesR MRM | lld:pubmed |
| pubmed-article:12011119 | pubmed:author | pubmed-author:GabrielsonEE | lld:pubmed |
| pubmed-article:12011119 | pubmed:author | pubmed-author:VañoEE | lld:pubmed |
| pubmed-article:12011119 | pubmed:author | pubmed-author:BemisLL | lld:pubmed |
| pubmed-article:12011119 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:12011119 | pubmed:day | 15 | lld:pubmed |
| pubmed-article:12011119 | pubmed:volume | 20 | lld:pubmed |
| pubmed-article:12011119 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:12011119 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:12011119 | pubmed:pagination | 2417-28 | lld:pubmed |
| pubmed-article:12011119 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:12011119 | pubmed:year | 2002 | lld:pubmed |
| pubmed-article:12011119 | pubmed:articleTitle | High-throughput tissue microarray analysis used to evaluate biology and prognostic significance of the E-cadherin pathway in non-small-cell lung cancer. | lld:pubmed |
| pubmed-article:12011119 | pubmed:affiliation | Department of Pathology, Division of Medical Oncology, University of Colorado Cancer Center, Denver, CO, USA. roy.bremnes@rito.no | lld:pubmed |
| pubmed-article:12011119 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:12011119 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:12011119 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:12011119 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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