| pubmed-article:19604089 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19604089 | lifeskim:mentions | umls-concept:C1516213 | lld:lifeskim |
| pubmed-article:19604089 | lifeskim:mentions | umls-concept:C0035647 | lld:lifeskim |
| pubmed-article:19604089 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:19604089 | lifeskim:mentions | umls-concept:C0027947 | lld:lifeskim |
| pubmed-article:19604089 | lifeskim:mentions | umls-concept:C1881878 | lld:lifeskim |
| pubmed-article:19604089 | lifeskim:mentions | umls-concept:C0123931 | lld:lifeskim |
| pubmed-article:19604089 | lifeskim:mentions | umls-concept:C1709518 | lld:lifeskim |
| pubmed-article:19604089 | lifeskim:mentions | umls-concept:C0332293 | lld:lifeskim |
| pubmed-article:19604089 | pubmed:issue | 7 | lld:pubmed |
| pubmed-article:19604089 | pubmed:dateCreated | 2009-7-16 | lld:pubmed |
| pubmed-article:19604089 | pubmed:abstractText | A recent study found that variation in camptothecin pharmacodynamic genes (TOP1, PARP1, TDP1 and XRCC1) correlated with efficacy and risk of neutropenia in irinotecan-treated cancer patients (median dose: 180 mg/m2), which suggests that these genes might predict outcomes to irinotecan-based therapies. The present study was conducted to evaluate previous gene associations using an independent sample of patients receiving irinotecan. | lld:pubmed |
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| pubmed-article:19604089 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:19604089 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:19604089 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19604089 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:19604089 | pubmed:issn | 1744-8042 | lld:pubmed |
| pubmed-article:19604089 | pubmed:author | pubmed-author:RatainMark... | lld:pubmed |
| pubmed-article:19604089 | pubmed:author | pubmed-author:RosnerGary... | lld:pubmed |
| pubmed-article:19604089 | pubmed:author | pubmed-author:McLeodHoward... | lld:pubmed |
| pubmed-article:19604089 | pubmed:author | pubmed-author:InnocentiFede... | lld:pubmed |
| pubmed-article:19604089 | pubmed:author | pubmed-author:HoskinsJanell... | lld:pubmed |
| pubmed-article:19604089 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19604089 | pubmed:volume | 10 | lld:pubmed |
| pubmed-article:19604089 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19604089 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19604089 | pubmed:pagination | 1139-46 | lld:pubmed |
| pubmed-article:19604089 | pubmed:dateRevised | 2011-6-14 | lld:pubmed |
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| pubmed-article:19604089 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19604089 | pubmed:articleTitle | Pharmacodynamic genes do not influence risk of neutropenia in cancer patients treated with moderately high-dose irinotecan. | lld:pubmed |
| pubmed-article:19604089 | pubmed:affiliation | UNC Institute for Pharmacogenomics & Individualized Therapy, University of North Carolina, Genetic Medicine Building, Chapel Hill, NC 27599-7360, USA. janelle_hoskins@unc.edu | lld:pubmed |
| pubmed-article:19604089 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:19604089 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:19604089 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:19604089 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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