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The CYP2D gene subfamily: analysis of the molecular basis of the debrisoquine 4-hydroxylase deficiency in DA rats

Data up to Jan 2025

Published1989
Citations99
References35

Total Citations Per Year

Abstract

References (35)

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Two mutant alleles of the human cytochrome P-450db1 gene (P450C2D1) associated with genetically deficient metabolism of debrisoquine and other drugs.

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Purification and characterization of the rat liver microsomal cytochrome P-450 involved in the 4-hydroxylation of debrisoquine, a prototype for genetic variation in oxidative drug metabolism

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Animal modelling of human polymorphic drug oxidation—the metabolism of debrisoquine and phenacetin in rat inbred strains

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Debrisoquine 4-Hydroxylase: Characterization of a New P450 Gene Subfamily, Regulation, Chromosomal Mapping, and Molecular Analysis of the DA Rat Polymorphism

1987 • 139 citations

Gene conversion in a cytochrome P-450 gene family.

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Sex and strain differences in hepatic debrisoquine 4-hydroxylase activity of the rat.

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At least six forms of extremely homologous cytochromes P-450 in rat liver are encoded at two closely linked genetic loci.

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Bufuralol 1'-hydroxylase activity of the rat

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Polymorphisms of four hepatic cytochromes P-450 in twenty-eight inbred strains of rat

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The CYP2D gene subfamily: analysis of the molecular basis of the debrisoquine… (1989) – Biochemistry | Metascience Observatory Explorer