4404333

Source:http://linkedlifedata.com/resource/pubmed/id/4404333

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0013227, umls-concept:C0020364, umls-concept:C0023884, umls-concept:C0205198, umls-concept:C0205227, umls-concept:C0815014, umls-concept:C0871161, umls-concept:C1517294, umls-concept:C1710236
pubmed:issue	5
pubmed:dateCreated	1973-1-5
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0035623
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Ammonium Sulfate, http://linkedlifedata.com/resource/pubmed/chemical/Benzopyrenes, http://linkedlifedata.com/resource/pubmed/chemical/Bile Acids and Salts, http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome P-450 Enzyme System, http://linkedlifedata.com/resource/pubmed/chemical/Cytochrome c Group, http://linkedlifedata.com/resource/pubmed/chemical/Cytochromes, http://linkedlifedata.com/resource/pubmed/chemical/Lipids, http://linkedlifedata.com/resource/pubmed/chemical/Methylcholanthrene, http://linkedlifedata.com/resource/pubmed/chemical/Mixed Function Oxygenases, http://linkedlifedata.com/resource/pubmed/chemical/NAD, http://linkedlifedata.com/resource/pubmed/chemical/NADP, http://linkedlifedata.com/resource/pubmed/chemical/Oxidoreductases, http://linkedlifedata.com/resource/pubmed/chemical/Phenobarbital, http://linkedlifedata.com/resource/pubmed/chemical/Phosphatidylcholines, http://linkedlifedata.com/resource/pubmed/chemical/Surface-Active Agents
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	0026-895X
pubmed:author	pubmed-author:LuA YAY, pubmed-author:WestS BSB
pubmed:issnType	Print
pubmed:volume	8
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	490-500
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:4404333-Ammonium Sulfate, pubmed-meshheading:4404333-Animals, pubmed-meshheading:4404333-Benzopyrenes, pubmed-meshheading:4404333-Bile Acids and Salts, pubmed-meshheading:4404333-Catalysis, pubmed-meshheading:4404333-Chemical Precipitation, pubmed-meshheading:4404333-Cytochrome P-450 Enzyme System, pubmed-meshheading:4404333-Cytochrome c Group, pubmed-meshheading:4404333-Cytochromes, pubmed-meshheading:4404333-Enzyme Activation, pubmed-meshheading:4404333-Hydrogen-Ion Concentration, pubmed-meshheading:4404333-Kinetics, pubmed-meshheading:4404333-Lipids, pubmed-meshheading:4404333-Male, pubmed-meshheading:4404333-Methylcholanthrene, pubmed-meshheading:4404333-Microsomes, Liver, pubmed-meshheading:4404333-Mixed Function Oxygenases, pubmed-meshheading:4404333-NAD, pubmed-meshheading:4404333-NADP, pubmed-meshheading:4404333-Oxidoreductases, pubmed-meshheading:4404333-Phenobarbital, pubmed-meshheading:4404333-Phosphatidylcholines, pubmed-meshheading:4404333-Rats, pubmed-meshheading:4404333-Surface-Active Agents
pubmed:year	1972
pubmed:articleTitle	Reconstituted liver microsomal enzyme system that hydroxylates drugs, other foreign compounds, and endogenous substrates. 3. Properties of the reconstituted 3,4-benzypyrene hydroxylase system.
pubmed:publicationType	Journal Article