Single-step assays to analyze CYP2D6 gene polymorphisms in Asians: allele frequencies and a novel *14B allele in mainland Chinese.
暂无分享,去创建一个
Ling Ji | M. Hersberger | K. Rentsch | J. Marti‐Jaun | Shixiu Pan | Jacqueline Marti-Jaun | Edgar Hänseler | Katharina Rentsch | Martin Hersberger | Shixiu Pan | L. Ji | E. Hänseler | Jacqueline Marti‐Jaun
[1] J. Weide,et al. Ultrarapid drug metabolism: PCR-based detection of CYP2D6 gene duplication. , 1998, Clinical chemistry.
[2] M. Ingelman-Sundberg,et al. Ultrarapid hydroxylation of debrisoquine in a Swedish population. Analysis of the molecular genetic basis. , 1995, The Journal of pharmacology and experimental therapeutics.
[3] F. Green,et al. Allele specific amplification by tetra-primer PCR. , 1992, Nucleic acids research.
[4] E. Skjelbo,et al. Phenotypes and genotypes for CYP2D6 and CYP2C19 in a black Tanzanian population. , 1999, British journal of clinical pharmacology.
[5] Y. Wing,et al. Occurrence of CYP2D6 gene duplication in Hong Kong Chinese. , 2000, Clinical chemistry.
[6] L. Bertilsson,et al. Pharmacokinetics of nortriptyline and its 10‐hydroxy metabolite in Chinese subjects of different CYP2D6 genotypes , 1998, Clinical pharmacology and therapeutics.
[7] A. Daly,et al. Molecular basis of polymorphic drug metabolism , 1995, Journal of Molecular Medicine.
[8] M. Ingelman-Sundberg,et al. Nomenclature for human CYP2D6 alleles. , 1996, Pharmacogenetics.
[9] J. Idle,et al. The cytochrome P450 CYP2D6 allelic variant CYP2D6J and related polymorphisms in a European population. , 1994, Pharmacogenetics.
[10] M. Ingelman-Sundberg,et al. Ultrarapid metabolism of sparteine: frequency of alleles with duplicated CYP2D6 genes in a Danish population as determined by restriction fragment length polymorphism and long polymerase chain reaction. , 1998, Pharmacogenetics.
[11] R. Prough,et al. Pharmacogenetics: a laboratory tool for optimizing therapeutic efficiency. , 1997, Clinical chemistry.
[12] J. Lafitte,et al. Polymorphism of the cytochrome P450 CYP2D6 gene in a European population: characterization of 48 mutations and 53 alleles, their frequencies and evolution. , 1997, Pharmacogenetics.
[13] A. Molven,et al. Ultrarapid metabolizers of debrisoquine: Characterization and PCR‐based detection of alleles with duplication of the CYP2D6 gene , 1996, FEBS letters.
[14] Edmund Lee,et al. OXIDATION PHENOTYPING IN CHINESE AND MALAY POPULATIONS , 1988, Clinical and experimental pharmacology & physiology.
[15] U. Gundert-Remy,et al. Hydroxylation polymorphisms of debrisoquine and mephenytoin in European populations , 2004, European Journal of Clinical Pharmacology.
[16] M. Hersberger,et al. Rapid detection of the CYP2D6*3, CYP2D6*4, and CYP2D6*6 alleles by tetra-primer PCR and of the CYP2D6*5 allele by multiplex long PCR. , 2000, Clinical chemistry.
[17] M. Lai,et al. Pharmacokinetics of metoprolol enantiomers in Chinese subjects of major CYP2D6 genotypes , 1999, Clinical pharmacology and therapeutics.
[18] M. Subrahmanyam. Storage of skin grafts in honey , 1993, The Lancet.
[19] L. Bertilsson,et al. Genetic analysis of the CYP2D locus in relation to debrisoquine hydroxylation capacity in Korean, Japanese and Chinese subjects. , 1995, Pharmacogenetics.
[20] A. Molven,et al. Polymorphisms in CYP2D6 duplication-negative individuals with the ultrarapid metabolizer phenotype: a role for the CYP2D6*35 allele in ultrarapid metabolism? , 2001, Pharmacogenetics.
[21] L. Bertilsson,et al. Pronounced differences between native Chinese and Swedish populations in the polymorphic hydroxylations of debrisoquin and S‐mephenytoin , 1992, Clinical pharmacology and therapeutics.
[22] M. Lai,et al. Molecular basis of genetic variation in debrisoquin hydroxylation in Chinese subjects: Polymorphism in RFLP and DNA sequence of CYP2D6 , 1993, Clinical pharmacology and therapeutics.
[23] E. Lee,et al. Frequency of human CYP2D6 mutant alleles in a normal Chinese population. , 1994, British journal of clinical pharmacology.
[24] M Schwab,et al. Comprehensive analysis of the genetic factors determining expression and function of hepatic CYP2D6. , 2001, Pharmacogenetics.
[25] M. Ingelman-Sundberg,et al. PCR-based genotyping for duplicated and deleted CYP2D6 genes. , 1996, Pharmacogenetics.
[26] H K Kroemer,et al. "It's the genes, stupid". Molecular bases and clinical consequences of genetic cytochrome P450 2D6 polymorphism. , 1995, Life sciences.
[27] M. Ingelman-Sundberg,et al. Genetic analysis of the Chinese cytochrome P4502D locus: characterization of variant CYP2D6 genes present in subjects with diminished capacity for debrisoquine hydroxylation. , 1994, Molecular pharmacology.
[28] M. Ingelman-Sundberg,et al. Molecular basis for rational megaprescribing in ultrarapid hydroxylators of debrisoquine , 1993, The Lancet.
[29] M. Lai,et al. G169R mutation diminishes the metabolic activity of CYP2D6 in Chinese. , 1999, Drug metabolism and disposition: the biological fate of chemicals.
[30] R. T. Coutts,et al. Polymorphic Cytochromes P450 and Drugs Used in Psychiatry , 1999, Cellular and Molecular Neurobiology.
[31] U. Meyer,et al. Evolution of a highly polymorphic human cytochrome P450 gene cluster: CYP2D6. , 1992, Genomics.
[32] J. Brockmöller,et al. Cytochrome P450 2D6 variants in a Caucasian population: allele frequencies and phenotypic consequences. , 1997, American journal of human genetics.
[33] M. Ingelman-Sundberg,et al. Inherited amplification of an active gene in the cytochrome P450 CYP2D locus as a cause of ultrarapid metabolism of debrisoquine. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[34] M Ingelman-Sundberg,et al. Frequent distribution of ultrarapid metabolizers of debrisoquine in an ethiopian population carrying duplicated and multiduplicated functional CYP2D6 alleles. , 1996, The Journal of pharmacology and experimental therapeutics.
[35] R. Tyndale,et al. Cytochrome P450 2D6.1 and cytochrome P450 2D6.10 differ in catalytic activity for multiple substrates. , 2001, Pharmacogenetics.
[36] M Ingelman-Sundberg,et al. Frequent occurrence of CYP2D6 gene duplication in Saudi Arabians. , 1997, Pharmacogenetics.
[37] J. Benítez,et al. Prevalence of CYP2D6 gene duplication and its repercussion on the oxidative phenotype in a white population , 1995, Clinical pharmacology and therapeutics.
[38] K L Lam,et al. Genetic analysis of the CYP2D6 locus in a Hong Kong Chinese population. , 2000, Clinical chemistry.