| pubmed-article:10734022 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:10734022 | lifeskim:mentions | umls-concept:C0087111 | lld:lifeskim |
| pubmed-article:10734022 | lifeskim:mentions | umls-concept:C0021390 | lld:lifeskim |
| pubmed-article:10734022 | lifeskim:mentions | umls-concept:C0000618 | lld:lifeskim |
| pubmed-article:10734022 | lifeskim:mentions | umls-concept:C0242485 | lld:lifeskim |
| pubmed-article:10734022 | lifeskim:mentions | umls-concept:C0870883 | lld:lifeskim |
| pubmed-article:10734022 | lifeskim:mentions | umls-concept:C1138555 | lld:lifeskim |
| pubmed-article:10734022 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:10734022 | pubmed:dateCreated | 2000-4-18 | lld:pubmed |
| pubmed-article:10734022 | pubmed:abstractText | The effects of 6-mercaptopurine (6-MP) are mediated via its intracellular conversion to 6-thioguanine (6-TG) and 6-methylmercaptopurine (6-MMP) nucleotide metabolites, the latter genetically controlled by thiopurine methyltransferase (TPMT). We sought to determine optimal therapeutic 6-MP metabolite levels and their correlation with medication-induced toxicity and TPMT genotype. | lld:pubmed |
| pubmed-article:10734022 | pubmed:language | eng | lld:pubmed |
| pubmed-article:10734022 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10734022 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:10734022 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:10734022 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:10734022 | pubmed:issn | 0016-5085 | lld:pubmed |
| pubmed-article:10734022 | pubmed:author | pubmed-author:YangH YHY | lld:pubmed |
| pubmed-article:10734022 | pubmed:author | pubmed-author:TarganS RSR | lld:pubmed |
| pubmed-article:10734022 | pubmed:author | pubmed-author:SinnettDD | lld:pubmed |
| pubmed-article:10734022 | pubmed:author | pubmed-author:ThéorêtYY | lld:pubmed |
| pubmed-article:10734022 | pubmed:author | pubmed-author:SeidmanE GEG | lld:pubmed |
| pubmed-article:10734022 | pubmed:author | pubmed-author:DubinskyM CMC | lld:pubmed |
| pubmed-article:10734022 | pubmed:author | pubmed-author:LamotheSS | lld:pubmed |
| pubmed-article:10734022 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:10734022 | pubmed:volume | 118 | lld:pubmed |
| pubmed-article:10734022 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:10734022 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:10734022 | pubmed:pagination | 705-13 | lld:pubmed |
| pubmed-article:10734022 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:10734022 | pubmed:year | 2000 | lld:pubmed |
| pubmed-article:10734022 | pubmed:articleTitle | Pharmacogenomics and metabolite measurement for 6-mercaptopurine therapy in inflammatory bowel disease. | lld:pubmed |
| pubmed-article:10734022 | pubmed:affiliation | Division of Gastroenterology and Nutrition, University of Montréal, Montréal, Québec, Canada. | lld:pubmed |
| pubmed-article:10734022 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:10734022 | pubmed:publicationType | Clinical Trial | lld:pubmed |
| pubmed-article:10734022 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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