pubmed-article:19284605 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19284605 | lifeskim:mentions | umls-concept:C0027819 | lld:lifeskim |
pubmed-article:19284605 | lifeskim:mentions | umls-concept:C0026809 | lld:lifeskim |
pubmed-article:19284605 | lifeskim:mentions | umls-concept:C0597032 | lld:lifeskim |
pubmed-article:19284605 | lifeskim:mentions | umls-concept:C0014257 | lld:lifeskim |
pubmed-article:19284605 | lifeskim:mentions | umls-concept:C2349967 | lld:lifeskim |
pubmed-article:19284605 | lifeskim:mentions | umls-concept:C0431085 | lld:lifeskim |
pubmed-article:19284605 | lifeskim:mentions | umls-concept:C0684321 | lld:lifeskim |
pubmed-article:19284605 | lifeskim:mentions | umls-concept:C0599894 | lld:lifeskim |
pubmed-article:19284605 | pubmed:dateCreated | 2009-4-10 | lld:pubmed |
pubmed-article:19284605 | pubmed:abstractText | High-risk neuroblastoma has an overall five-year survival of less than 40%, indicating a need for new treatment strategies such as angiogenesis inhibition. Recent studies have shown that chemotherapeutic drugs can inhibit angiogenesis if administered in a continuous schedule. The aim of this study was primarily to characterize tumor spread in an orthotopic, metastatic model for aggressive, MYCN-amplified neuroblastoma and secondarily to study the effects of daily administration of the chemotherapeutic agent CHS 828 on tumor angiogenesis, tumor growth, and spread. | lld:pubmed |
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pubmed-article:19284605 | pubmed:language | eng | lld:pubmed |
pubmed-article:19284605 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19284605 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:19284605 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:19284605 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19284605 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:19284605 | pubmed:issn | 1479-5876 | lld:pubmed |
pubmed-article:19284605 | pubmed:author | pubmed-author:StridsbergMat... | lld:pubmed |
pubmed-article:19284605 | pubmed:author | pubmed-author:Christofferso... | lld:pubmed |
pubmed-article:19284605 | pubmed:author | pubmed-author:AzarbayjaniFa... | lld:pubmed |
pubmed-article:19284605 | pubmed:author | pubmed-author:LindhagenElin... | lld:pubmed |
pubmed-article:19284605 | pubmed:author | pubmed-author:FuchsDieterD | lld:pubmed |
pubmed-article:19284605 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:19284605 | pubmed:volume | 7 | lld:pubmed |
pubmed-article:19284605 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:19284605 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:19284605 | pubmed:pagination | 16 | lld:pubmed |
pubmed-article:19284605 | pubmed:dateRevised | 2010-9-23 | lld:pubmed |
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pubmed-article:19284605 | pubmed:year | 2009 | lld:pubmed |
pubmed-article:19284605 | pubmed:articleTitle | Regression of orthotopic neuroblastoma in mice by targeting the endothelial and tumor cell compartments. | lld:pubmed |
pubmed-article:19284605 | pubmed:affiliation | Department of Medical Cell Biology, Uppsala University, 75123 Uppsala, Sweden. dieter.fuchs@mcb.uu.se | lld:pubmed |
pubmed-article:19284605 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:19284605 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |