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Inherited amplification of an active gene in the cytochrome P450 CYP2D locus as a cause of ultrarapid metabolism of debrisoquine.

Data up to Jan 2025

Published1993
Citations652
References21

Total Citations Per Year

Abstract

References (21)

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GENE AMPLIFICATION

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Deletion of the entire cytochrome P450 CYP2D6 gene as a cause of impaired drug metabolism in poor metabolizers of the debrisoquine/sparteine polymorphism.

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Multiple mutations of the human cytochrome P450IID6 gene (CYP2D6) in poor metabolizers of debrisoquine. Study of the functional significance of individual mutations by expression of chimeric genes.

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DNA amplification is rare in normal human cells.

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Human debrisoquine 4-hydroxylase (P450IID1): cDNA and deduced amino acid sequence and assignment of the CYP2D locus to chromosome 22

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Extremely Rapid Hydroxylation of Debrisoquine

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De novo amplification within a "silent" human cholinesterase gene in a family subjected to prolonged exposure to organophosphorous insecticides.

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Inherited amplification of an active gene in the cytochrome P450 CYP2D locus as a cause… (1993) – Proceedings of the National Academy of Sciences | Metascience Observatory Explorer