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Pharmacopsychiatry|July 11, 2002
Cytochrome P450 2D6 deficiency and its clinical relevance in a patient treated with risperidoneM D Köhnke, E-U Griese, D Stösser, et al.
Pharmacogenetics|January 14, 2000
Analysis of the CYP2D6 gene mutations and their consequences for enzyme function in a West African populationE U Griese, S Asante-Poku, D Ofori-Adjei, et al.
Pharmacogenetics|October 1, 1996
Rapid detection of CYP2D6 null alleles by long distance- and multiplex-polymerase chain reactionT Stüven, E U Griese, H K Kroemer, et al.
Human Genetics|January 1, 1987
Hemoglobin M Iwate is caused by a C----T transition in codon 87 of the human alpha 1-globin geneJ Horst, G Assum, E U Griese, et al.
Pharmacogenetics|October 19, 2000
Elucidation of the genetic basis of the common 'intermediate metabolizer' phenotype for drug oxidation by CYP2D6S Raimundo, J Fischer, M Eichelbaum, et al.
British Journal of Clinical Pharmacology|September 1, 1996
Expression of CYP3A4, CYP3A5 and CYP3A7 in human duodenal tissueK T Kivistö, G Bookjans, M F Fromm, et al.
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