| pubmed-article:15842554 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15842554 | lifeskim:mentions | umls-concept:C0008287 | lld:lifeskim |
| pubmed-article:15842554 | lifeskim:mentions | umls-concept:C1332828 | lld:lifeskim |
| pubmed-article:15842554 | lifeskim:mentions | umls-concept:C1332829 | lld:lifeskim |
| pubmed-article:15842554 | lifeskim:mentions | umls-concept:C0032529 | lld:lifeskim |
| pubmed-article:15842554 | lifeskim:mentions | umls-concept:C0743223 | lld:lifeskim |
| pubmed-article:15842554 | lifeskim:mentions | umls-concept:C1533691 | lld:lifeskim |
| pubmed-article:15842554 | pubmed:issue | 5 | lld:pubmed |
| pubmed-article:15842554 | pubmed:dateCreated | 2005-4-21 | lld:pubmed |
| pubmed-article:15842554 | pubmed:abstractText | We evaluated the involvement of cytochrome P450 (CYP) isoforms 2C9 and 2C19 in chlorpropamide 2-hydroxylation in vitro and in chlorpropamide disposition in vivo. | lld:pubmed |
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| pubmed-article:15842554 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:15842554 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:15842554 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15842554 | pubmed:month | May | lld:pubmed |
| pubmed-article:15842554 | pubmed:issn | 0306-5251 | lld:pubmed |
| pubmed-article:15842554 | pubmed:author | pubmed-author:LiuKwang-Hyeo... | lld:pubmed |
| pubmed-article:15842554 | pubmed:author | pubmed-author:ShonJi-HongJH | lld:pubmed |
| pubmed-article:15842554 | pubmed:author | pubmed-author:YoonYoung-Ran... | lld:pubmed |
| pubmed-article:15842554 | pubmed:author | pubmed-author:KimKyoung-AhK... | lld:pubmed |
| pubmed-article:15842554 | pubmed:author | pubmed-author:LimYoung-Chae... | lld:pubmed |
| pubmed-article:15842554 | pubmed:author | pubmed-author:ChaIn-JuneIJ | lld:pubmed |
| pubmed-article:15842554 | pubmed:author | pubmed-author:ShinJae-GookJ... | lld:pubmed |
| pubmed-article:15842554 | pubmed:author | pubmed-author:ShinDong-Hoon... | lld:pubmed |
| pubmed-article:15842554 | pubmed:author | pubmed-author:KimMin-JungMJ | lld:pubmed |
| pubmed-article:15842554 | pubmed:author | pubmed-author:LeeChung... | lld:pubmed |
| pubmed-article:15842554 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15842554 | pubmed:volume | 59 | lld:pubmed |
| pubmed-article:15842554 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15842554 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15842554 | pubmed:pagination | 552-63 | lld:pubmed |
| pubmed-article:15842554 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:15842554 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:15842554 | pubmed:articleTitle | Chlorpropamide 2-hydroxylation is catalysed by CYP2C9 and CYP2C19 in vitro: chlorpropamide disposition is influenced by CYP2C9, but not by CYP2C19 genetic polymorphism. | lld:pubmed |
| pubmed-article:15842554 | pubmed:affiliation | Department of Pharmacology and PharmacoGenomics Research Centre, Inje University College of Medicine and Clinical Pharmacology Centre, Busan Paik Hospital, Busan 641-735, Korea. | lld:pubmed |
| pubmed-article:15842554 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15842554 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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