scholarly article | Q13442814 |
P50 | author | Adrián Llerena | Q56419301 |
P2093 | author name string | Lindström L | |
Bertilsson L | |||
Dahl ML | |||
Bondesson U | |||
P2860 | cites work | A family and population study of the genetic polymorphism of debrisoquine oxidation in a white British population. | Q33667784 |
Clozapine for the treatment-resistant schizophrenic. A double-blind comparison with chlorpromazine | Q34048732 | ||
Polymorphic hydroxylation of Debrisoquine in man. | Q34057031 | ||
Pronounced differences between native Chinese and Swedish populations in the polymorphic hydroxylations of debrisoquin and S-mephenytoin | Q34241704 | ||
Dopamine receptor sequences. Therapeutic levels of neuroleptics occupy D2 receptors, clozapine occupies D4 | Q35275118 | ||
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Disposition of the neuroleptic zuclopenthixol cosegregates with the polymorphic hydroxylation of debrisoquine in humans | Q43607538 | ||
Determination of clozapine and its N-demethylated metabolite in plasma by use of gas chromatography-mass spectrometry with single ion detection | Q43794493 | ||
MPTP, the neurotoxin inducing Parkinson's disease, is a potent competitive inhibitor of human and rat cytochrome P450 isozymes (P450bufI, P450db1) catalyzing debrisoquine 4-hydroxylation | Q48183426 | ||
Is the sigma opiate receptor a proadifen-sensitive subform of cytochrome P-450? | Q48944016 | ||
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SKF 525-A and cytochrome P-450 ligands inhibit with high affinity the binding of [3H]dextromethorpan and σ ligands to guinea pig brain | Q53867774 | ||
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Exchange of aromatically bound halogen for OH- and SCH3-groups in metabolising clozapine in the human organism (author's transl) | Q67022219 | ||
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Clinical pharmacokinetics of clozapine in chronic schizophrenic patients | Q67989786 | ||
The antipsychotic clozapine is metabolized by the polymorphic human microsomal and recombinant cytochrome P450 2D6 | Q68071363 | ||
Multiple-dose pharmacokinetics of clozapine in patients | Q68853598 | ||
S-mephenytoin hydroxylation phenotypes in a Swedish population determined after coadministration with debrisoquin | Q69610224 | ||
Disposition of perphenazine is related to polymorphic debrisoquin hydroxylation in human beings | Q69649340 | ||
Dose-related plasma levels of clozapine: influence of smoking behaviour, sex and age | Q69795312 | ||
Plasma levels of thioridazine and metabolites are influenced by the debrisoquin hydroxylation phenotype | Q70123367 | ||
Absence of hepatic cytochrome P450bufI causes genetically deficient debrisoquine oxidation in man | Q70219763 | ||
The metabolism of 8-chloro-11-(4-methyl-1-piperazinyl)-5H-dibenzo(b,e) (1,4)diazepine (clozapine) in mice, dogs and human subjects | Q70707284 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 71-74 | |
P577 | publication date | 1994-01-01 | |
P1433 | published in | British Journal of Clinical Pharmacology | Q176044 |
P1476 | title | Disposition of clozapine in man: lack of association with debrisoquine and S-mephenytoin hydroxylation polymorphisms | |
P478 | volume | 37 |
Q80967258 | A Kinetic Model for Simultaneous Fit of Clozapine and Norclozapine Concentrations in Chronic Schizophrenic Patients during Long-Term Treatment |
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Q57719513 | Analysis of clozapine response and polymorphisms of the dopamine D4 receptor gene (DRD4) in schizophrenic patients |
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Q33916981 | Clinically significant pharmacokinetic interactions between dietary caffeine and medications |
Q43201721 | Clozapine disposition covaries with CYP1A2 activity determined by a caffeine test |
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