CYP2D6, SULT1A1 and UGT2B17 copy number variation: quantitative detection by multiplex PCR.
about
A novel simple method for determining CYP2D6 gene copy number and identifying allele(s) with duplication/multiplicationDistribution of CYP2D6 alleles and phenotypes in the Brazilian populationDiversity Outbred Mice Identify Population-Based Exposure Thresholds and Genetic Factors that Influence Benzene-Induced Genotoxicity.Detection of an endogenous urinary biomarker associated with CYP2D6 activity using global metabolomicsCYP2D6 Haplotype Determination Using Long Range Allele-Specific Amplification: Resolution of a Complex Genotype and a Discordant Genotype Involving the CYP2D6*59 Allele.Multi-ethnic cytochrome-P450 copy number profiling: novel pharmacogenetic alleles and mechanism of copy number variation formation.Single dose, CYP2D6 genotype-stratified pharmacokinetic study of atomoxetine in children with ADHDSULT2A1 Gene Copy Number Variation is Associated with Urinary Excretion Rate of Steroid Sulfates.Characterization of Atomoxetine Biotransformation and Implications for Development of PBPK Models for Dose Individualization in Children.Common CYP2D6 polymorphisms affecting alternative splicing and transcription: long-range haplotypes with two regulatory variants modulate CYP2D6 activity.High-resolution melt analysis to detect sequence variations in highly homologous gene regions: application to CYP2B6.Characterization of ADME gene variation in 21 populations by exome sequencing.Impact of metabolizing enzymes on drug response of endocrine therapy in breast cancer.Complexities of CYP2D6 gene analysis and interpretation.Association between CYP2D6 Genotypes and the Risk of Antidepressant Discontinuation, Dosage Modification and the Occurrence of Maternal Depression during Pregnancy.Methyleugenol DNA adducts in human liver are associated with SULT1A1 copy number variations and expression levels.QTL Mapping and Identification of Candidate Genes in DO Mice: A Use Case Model Derived from a Benzene Toxicity Experiment.CYP2A6 genotyping methods and strategies using real-time and end point PCR platforms.CYP2D6 and pharmacogenomics: where does future research need to focus? Part 1: technical aspects.Characterization of the CYP2D6 gene locus and metabolic activity in Indo- and Afro-Trinidadians: discovery of novel allelic variants.Constellation: a tool for rapid, automated phenotype assignment of a highly polymorphic pharmacogene, CYP2D6, from whole-genome sequences.Incorporating population-level genetic variability within laboratory models in toxicology: From the individual to the population.Copy number variation and gene rearrangements in CYP2D6 genotyping using multiplex ligation-dependent probe amplification in Koreans.Sulfotransferase 1A3/4 copy number variation is associated with neurodegenerative disease.Frequency of CYP2D6 Alleles Including Structural Variants in the United States.
P2860
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P2860
CYP2D6, SULT1A1 and UGT2B17 copy number variation: quantitative detection by multiplex PCR.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh
2011年學術文章
@zh-hant
name
CYP2D6, SULT1A1 and UGT2B17 co ...... ve detection by multiplex PCR.
@en
CYP2D6, SULT1A1 and UGT2B17 co ...... ve detection by multiplex PCR.
@nl
type
label
CYP2D6, SULT1A1 and UGT2B17 co ...... ve detection by multiplex PCR.
@en
CYP2D6, SULT1A1 and UGT2B17 co ...... ve detection by multiplex PCR.
@nl
prefLabel
CYP2D6, SULT1A1 and UGT2B17 co ...... ve detection by multiplex PCR.
@en
CYP2D6, SULT1A1 and UGT2B17 co ...... ve detection by multiplex PCR.
@nl
P2093
P2860
P356
P1433
P1476
CYP2D6, SULT1A1 and UGT2B17 co ...... ve detection by multiplex PCR.
@en
P2093
Andrea Gaedigk
Greyson P Twist
J Steven Leeder
P2860
P304
P356
10.2217/PGS.11.135
P577
2011-11-23T00:00:00Z