pubmed-article:12814462 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:12814462 | lifeskim:mentions | umls-concept:C0020365 | lld:lifeskim |
pubmed-article:12814462 | lifeskim:mentions | umls-concept:C0031013 | lld:lifeskim |
pubmed-article:12814462 | lifeskim:mentions | umls-concept:C1882417 | lld:lifeskim |
pubmed-article:12814462 | lifeskim:mentions | umls-concept:C1533691 | lld:lifeskim |
pubmed-article:12814462 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:12814462 | pubmed:dateCreated | 2003-6-19 | lld:pubmed |
pubmed-article:12814462 | pubmed:abstractText | The aims of this study were to examine the in vitro enzyme kinetics and CYP isoform selectivity of perhexiline monohydroxylation using human liver microsomes. | lld:pubmed |
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pubmed-article:12814462 | pubmed:language | eng | lld:pubmed |
pubmed-article:12814462 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:12814462 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:12814462 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:12814462 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:12814462 | pubmed:month | Jun | lld:pubmed |
pubmed-article:12814462 | pubmed:issn | 0306-5251 | lld:pubmed |
pubmed-article:12814462 | pubmed:author | pubmed-author:BirkettD JDJ | lld:pubmed |
pubmed-article:12814462 | pubmed:author | pubmed-author:SomogyiA AAA | lld:pubmed |
pubmed-article:12814462 | pubmed:author | pubmed-author:MinersJ OJO | lld:pubmed |
pubmed-article:12814462 | pubmed:author | pubmed-author:GrgurinovichN... | lld:pubmed |
pubmed-article:12814462 | pubmed:author | pubmed-author:SørensenL BLB | lld:pubmed |
pubmed-article:12814462 | pubmed:author | pubmed-author:SørensenR NRN | lld:pubmed |
pubmed-article:12814462 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:12814462 | pubmed:volume | 55 | lld:pubmed |
pubmed-article:12814462 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:12814462 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:12814462 | pubmed:pagination | 635-8 | lld:pubmed |
pubmed-article:12814462 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
pubmed-article:12814462 | pubmed:meshHeading | pubmed-meshheading:12814462... | lld:pubmed |
pubmed-article:12814462 | pubmed:meshHeading | pubmed-meshheading:12814462... | lld:pubmed |
pubmed-article:12814462 | pubmed:meshHeading | pubmed-meshheading:12814462... | lld:pubmed |
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pubmed-article:12814462 | pubmed:meshHeading | pubmed-meshheading:12814462... | lld:pubmed |
pubmed-article:12814462 | pubmed:meshHeading | pubmed-meshheading:12814462... | lld:pubmed |
pubmed-article:12814462 | pubmed:meshHeading | pubmed-meshheading:12814462... | lld:pubmed |
pubmed-article:12814462 | pubmed:meshHeading | pubmed-meshheading:12814462... | lld:pubmed |
pubmed-article:12814462 | pubmed:meshHeading | pubmed-meshheading:12814462... | lld:pubmed |
pubmed-article:12814462 | pubmed:year | 2003 | lld:pubmed |
pubmed-article:12814462 | pubmed:articleTitle | Polymorphic hydroxylation of perhexiline in vitro. | lld:pubmed |
pubmed-article:12814462 | pubmed:affiliation | Department of Clinical Pharmacology, Flinders Medical Centre and Flinders University of South Australia, Bedford Park, Australia. | lld:pubmed |
pubmed-article:12814462 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:12814462 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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