pubmed-article:16126463 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:16126463 | lifeskim:mentions | umls-concept:C0376358 | lld:lifeskim |
pubmed-article:16126463 | lifeskim:mentions | umls-concept:C1514559 | lld:lifeskim |
pubmed-article:16126463 | lifeskim:mentions | umls-concept:C0221198 | lld:lifeskim |
pubmed-article:16126463 | lifeskim:mentions | umls-concept:C0018270 | lld:lifeskim |
pubmed-article:16126463 | lifeskim:mentions | umls-concept:C1417753 | lld:lifeskim |
pubmed-article:16126463 | lifeskim:mentions | umls-concept:C1518633 | lld:lifeskim |
pubmed-article:16126463 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:16126463 | pubmed:dateCreated | 2006-2-6 | lld:pubmed |
pubmed-article:16126463 | pubmed:abstractText | Although a majority of metastatic prostate cancer lesions are osteoblastic in nature, some are mixed or lytic; and, osteoblastic lesions require osteolytic activity in order to progress. The role of BMPs in the formation of prostate cancer metastases to bone remains unknown. We hypothesized that BMPs influence the development and progression of osteolytic prostate cancer lesions. | lld:pubmed |
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pubmed-article:16126463 | pubmed:language | eng | lld:pubmed |
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pubmed-article:16126463 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:16126463 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:16126463 | pubmed:month | Feb | lld:pubmed |
pubmed-article:16126463 | pubmed:issn | 8756-3282 | lld:pubmed |
pubmed-article:16126463 | pubmed:author | pubmed-author:SchwarzEdward... | lld:pubmed |
pubmed-article:16126463 | pubmed:author | pubmed-author:LiebermanJay... | lld:pubmed |
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pubmed-article:16126463 | pubmed:author | pubmed-author:HsuWellington... | lld:pubmed |
pubmed-article:16126463 | pubmed:author | pubmed-author:FeeleyBrian... | lld:pubmed |
pubmed-article:16126463 | pubmed:author | pubmed-author:GamradtSeth... | lld:pubmed |
pubmed-article:16126463 | pubmed:author | pubmed-author:LiuNancyN | lld:pubmed |
pubmed-article:16126463 | pubmed:author | pubmed-author:KrenekLucieL | lld:pubmed |
pubmed-article:16126463 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:16126463 | pubmed:volume | 38 | lld:pubmed |
pubmed-article:16126463 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:16126463 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:16126463 | pubmed:pagination | 154-66 | lld:pubmed |
pubmed-article:16126463 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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pubmed-article:16126463 | pubmed:year | 2006 | lld:pubmed |
pubmed-article:16126463 | pubmed:articleTitle | Overexpression of noggin inhibits BMP-mediated growth of osteolytic prostate cancer lesions. | lld:pubmed |
pubmed-article:16126463 | pubmed:affiliation | Department of Orthopaedic Surgery, David Geffen School of Medicine at UCLA, Center for Health Sciences 76-134, 10833 LeConte Avenue, Los Angeles, CA 90095, USA. bfeeley@mednet.ucla.edu | lld:pubmed |
pubmed-article:16126463 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:16126463 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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