All Stories

  1. Lean body weight dosing avoids excessive systemic exposure to proton pump inhibitors for children with obesity
  2. Age- and Genotype-Dependent Variability in the Protein Abundance and Activity of Six Major Uridine Diphosphate-Glucuronosyltransferases in Human Liver
  3. Impact of SLCO1B1 Genotype on Pediatric Simvastatin Acid Pharmacokinetics
  4. Impact of CYP2D6 on venlafaxine metabolism in Trinidadian patients with major depressive disorder
  5. The Pharmacogene Variation (PharmVar) Consortium: Incorporation of the Human Cytochrome P450 (CYP ) Allele Nomenclature Database
  6. Variants in the CYP2B6 3′UTR Alter In Vitro and In Vivo CYP2B6 Activity: Potential Role of MicroRNAs
  7. In vivo characterization of CYP2D6*12, *29 and *84 using dextromethorphan as a probe drug: a case report
  8. Impact of CYP2D6 genotype on amitriptyline efficacy for the treatment of diabetic peripheral neuropathy: a pilot study
  9. CYP450 genotype and pharmacogenetic association studies: a critical appraisal
  10. Long-Read Single Molecule Real-Time Full Gene Sequencing of Cytochrome P450-2D6
  11. Developmental Expression of CYP2B6: A Comprehensive Analysis of mRNA Expression, Protein Content and Bupropion Hydroxylase Activity and the Impact of Genetic Variation
  12. Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting
  13. CYP2D6 Haplotype Determination Using Long Range Allele-Specific Amplification
  14. Pharmacogenetic comparison of CYP2D6 predictive and measured phenotypes in a South African cohort
  15. Age-Related Changes in MicroRNA Expression and Pharmacogenes in Human Liver
  16. Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline forCYP2D6andCYP2C19Genotypes and Dosing of Selective Serotonin Reuptake Inhibitors
  17. SNP genotyping using TaqMan® technology: the CYP2D6*17 assay conundrum
  18. Detection of an endogenous urinary biomarker associated with CYP2D6 activity using global metabolomics
  19. Resolution of a clinical AmpliChip CYP450 Test™ no call: discovery and characterization of novelCYP2D6*1haplotypes
  20. CYP2D6 and pharmacogenomics: where does future research need to focus? Part 2: clinical aspects
  21. Effect of CYP3A5 genotype, steroids, and azoles on tacrolimus in a pediatric renal transplant population
  22. Population Pharmacokinetics of Oral Baclofen in Pediatric Patients with Cerebral Palsy
  23. Challenges in CYP2D6 Phenotype Assignment from Genotype Data: A Critical Assessment and Call for Standardization
  24. CYP2D6 and pharmacogenomics: where does future research need to focus? Part 1: technical aspects
  25. Clinical Pharmacogenetics Implementation Consortium Guidelines for Cytochrome P450 2D6 Genotype and Codeine Therapy: 2014 Update
  26. Characterization of a complex CYP2D6 genotype that caused an AmpliChip CYP450 Test® no-call in the clinical setting
  27. Complexities ofCYP2D6gene analysis and interpretation
  28. Common CYP2D6 polymorphisms affecting alternative splicing and transcription: long-range haplotypes with two regulatory variants modulate CYP2D6 activity
  29. Regulation of MicroRNA Expression by Rifampin in Human Hepatocytes
  30. Pharmacogenetics in American Indian populations
  31. Polymorphisms in CYP2D6 may predict methamphetamine related heart failure
  32. High-resolution melt analysis to detect sequence variations in highly homologous gene regions: application to CYP2B6
  33. Characterization of the CYP2D6 gene locus and metabolic activity in Indo- and Afro-Trinidadians: discovery of novel allelic variants
  34. Clinical Pharmacogenetics Implementation Consortium Guideline for CYP2D6 and CYP2C19 Genotypes and Dosing of Tricyclic Antidepressants
  35. Introduction of the AmpliChip CYP450 Test to a South African cohort: a platform comparative prospective cohort study
  36. CYP2D6 update
  37. The neuroprotective enzyme CYP2D6 increases in the brain with age and is lower in Parkinson's disease patients
  38. Defining Risk Factors for Red Man Syndrome in Children and Adults
  39. In Silico and In Vitro Identification of MicroRNAs That Regulate Hepatic Nuclear Factor 4α Expression
  40. CYP2D6,SULT1A1andUGT2B17copy number variation: quantitative detection by multiplex PCR
  41. Clinical Pharmacogenetics Implementation Consortium (CPIC) Guidelines for Codeine Therapy in the Context of Cytochrome P450 2D6 (CYP2D6) Genotype
  42. Detection and characterization of theCYP2D6*9x2gene duplication in two Spanish populations: resolution of AmpliChip CYP450 test no-calls
  43. Genetic Transmission of Cytochrome P450 2D6 (CYP2D6) Ultrarapid Metabolism: Implications for Breastfeeding Women taking Codeine
  44. Relapse of depressive and anxiety symptoms, and quality-of-life in pregnant users and discontinued users of antidepressants: Results from the OTIS Antidepressants Study
  45. Erratum to: Discovery of the nonfunctional CYP2D6*31 allele in Spanish, Puerto Rican, and US Hispanic populations
  46. Assessment of Activity Levels for CYP2D6*1, CYP2D6*2, and CYP2D6*41 Genes by Population Pharmacokinetics of Dextromethorphan
  47. Systematic genetic and genomic analysis of cytochrome P450 enzyme activities in human liver
  48. Elucidation of CYP2D6 Genetic Diversity in a Unique African Population: Implications for the Future Application of Pharmacogenetics in the Xhosa Population
  49. Discovery of the nonfunctional CYP2D6*31 allele in Spanish, Puerto Rican, and US Hispanic populations
  50. Impact of the CYP2C19*17 Allele on the Pharmacokinetics of Omeprazole and Pantoprazole in Children: Evidence for a Differential Effect
  51. Variability in drug metabolizing enzyme activity in HIV-infected patients
  52. CYP2D7–2D6hybrid tandems: identification of novel CYP2D6 duplication arrangements and implications for phenotype prediction
  53. UGT2B17 and SULT1A1 gene copy number variation (CNV) detection by LabChip microfluidic technology
  54. Identification of Novel CYP2D7-2D6 Hybrids: Non-Functional and Functional Variants
  55. Maribavir Pharmacokinetics and the Effects of Multiple-Dose Maribavir on Cytochrome P450 (CYP) 1A2, CYP 2C9, CYP 2C19, CYP 2D6, CYP 3A, N-Acetyltransferase-2, and Xanthine Oxidase Activities in Healthy Adults
  56. Single-Dose Pharmacokinetics of Oral and Intravenous Pantoprazole in Children and Adolescents
  57. Reduced Activities of Cytochrome P450 1A2 and Xanthine Oxidase in Children With Growth Hormone Deficiency
  58. Genetic determinants of variable metabolism have little impact on the clinical use of leading antipsychotics in the CATIE study
  59. Identification of a novel non-functional CYP2D6 allele, CYP2D6*69, in a Caucasian poor metabolizer individual
  60. Evaluation of a [13C]-Dextromethorphan Breath Test to Assess CYP2D6 Phenotype
  61. Six-month, prospective, longitudinal, open-Label caffeine and dextromethorphan phenotyping study in children with growth hormone deficiency receiving recombinant human growth hormone replacement
  62. Pharmacogenetics of Neonatal Opioid Toxicity Following Maternal Use of Codeine During Breastfeeding: A Case–Control Study
  63. Molecular Therapeutics: 21st Century Medicine
  64. Interindividual variability in acetaminophen sulfation by human fetal liver: Implications for pharmacogenetic investigations of drug-induced birth defects
  65. The CYP2D6 gene locus in South African Coloureds: unique allele distributions, novel alleles and gene arrangements
  66. The CYP2D6 Activity Score: Translating Genotype Information into a Qualitative Measure of Phenotype
  67. Multilocus Genotyping Identifies Infections by Multiple Strains of Trichophyton tonsurans
  68. Effect of Arylamine Acetyltransferase Nat3 Gene Knockout on N-Acetylation in the Mouse
  69. Identification and Characterization of CYP2D6*56B, an Allele Associated with the Poor Metabolizer Phenotype
  70. Ontogeny of Dextromethorphan O- and N-demethylation in the First Year of Life
  71. Cytochrome P4502D6 (CYP2D6) Gene Locus Heterogeneity: Characterization of Gene Duplication Events
  72. Tracking Trichophyton tonsurans Through a Large Urban Child Care Center: Defining Infection Prevalence and Transmission Patterns by Molecular Strain Typing
  73. Reply
  74. Maternal Codeine is Not Safe for all Breast-Fed Infants
  75. Pharmacogenetics of morphine poisoning in a breastfed neonate of a codeine-prescribed mother
  76. Variability of CYP2J2 Expression in Human Fetal Tissues
  77. Effects of fluvastatin and cigarette smoking on CYP2C9 activity measured using the probe S-warfarin
  78. Maribavir Pharmacokinetics and the Effects of Multiple-Dose Maribavir on Cytochrome P450 (CYP) 1A2, CYP 2C9, CYP 2C19, CYP 2D6, CYP 3A, N-Acetyltransferase-2, and Xanthine Oxidase Activities in Healthy Adults
  79. PIII-32Characterization of CYP2D7 expression: Does a CYP2D7-derived functional gene product exist?
  80. OIV-B-2Chronic intermittent nocturnal hypoxemia alters activities of hepatic cytochrome P4501A2 (CYP1A2), N-acetyltransferase 2 (NAT2) and xanthine oxidase (XO) in children with obstructive sleep apnea (OSA)
  81. LBOVI-B-4Recombinant human growth hormone (rhGH) has no effect on activities of hepatic cytochrome P4501A2 (CYP1A2), N-acetyltransferase 2 (NAT2), xanthine oxidase (XO) or cytochrome P4502D6 in children with idiopathic growth hormone (GH) deficiency
  82. CYP2D6*36GENE ARRANGEMENTS WITHIN THECYP2D6LOCUS: ASSOCIATION OFCYP2D6*36WITH POOR METABOLIZER STATUS
  83. Effect of a Triphasic Oral Contraceptive on Drug-Metabolizing Enzyme Activity as Measured by the Validated Cooperstown 5+1 Cocktail
  84. Multiple Dose Pharmacokinetics of Paroxetine in Children and Adolescents with Major Depressive Disorder or Obsessive–Compulsive Disorder
  85. Identification of CYP2D6 impaired functional alleles in Mexican Americans
  86. CYP2D7 splice variants in human liver and brain: Does CYP2D7 encode functional protein?
  87. Characterization of the ALP1 Gene Locus of Trichophyton tonsurans
  88. Limited Association of the 2988g>a Single Nucleotide Polymorphism with CYP2D6*41 in Black Subjects
  89. Effect of the anti-cytomegalovirus (CMV) drug maribavir (MB) on the activities of cytochrome p450 (CYP) 1A2, 2C9, 2C19, 2D6, 3A, N-ACETYLTRANSFERASE-2 (NAT-2), and xanthine oxidase (XO) as assessed by the cooperstown 5+1 drug cocktail
  90. Identification and characterization of novel sequence variations in the cytochrome P4502D6 (CYP2D6) gene in African Americans
  91. Identification and characterization of novel sequence variations in the cytochrome P4502D6 (CYP2D6) gene in African Americans
  92. Pharmacokinetics and genotypes do not predict metoprolol adverse events or efficacy in hypertension
  93. Lack of Weight-Based Dose Dependency and Intraindividual Variability of Omeprazole for CYP2C19 Phenotyping
  94. Coadministration of Lopinavir/Ritonavir and Phenytoin Results in Two-Way Drug Interaction Through Cytochrome P-450 Induction
  95. Limited Sampling Strategy of S-Warfarin Concentrations, but Not Warfarin S/R Ratios, Accurately Predicts S-Warfarin AUC during Baseline and Inhibition in CYP2C9 Extensive Metabolizers
  96. Extensive alternative splicing of cytochrome P4502D6 (CYP2D6) mRNA: explanation for variability among subjects with identical genotypes?
  97. Genetic Heterogeneity in the rRNA Gene Locus of Trichophyton tonsurans
  98. Omeprazole Disposition in Children following Single-Dose Administration
  99. Discovery of a novel nonfunctional cytochrome P450 2D6 allele, CYP2D6*42, in African American subjects
  100. CYP2D6 Poor Metabolizer Status Can Be Ruled Out by a Single Genotyping Assay for the -1584G Promoter Polymorphism
  101. Evaluation of Inhibitory Effects of Metoclopramide (MET) on CYP2D6 Activity in Infants
  102. Characterization of an African American (AA) subject carrying two novel functional CYP2D6 alleles.
  103. Effect of cigarette smoking on CYP2C9 activity.
  104. Pantoprazole Disposition in Pediatrics
  105. Allelic variation of the pregnane X receptor (PXR) and CYP3A4 activity
  106. Variability in thiopurine methyltransferase (TPMT) and outcome in pediatric renal transplant patients.
  107. Effect of oral contraceptives (OCS) on drug metabolizing enzymes (DMES) as measured by the validated cooperstown 5+1 cocktail (5+1).
  108. Use of limited sampling strategy (LSS) of S-warfarin (S-W) concentrations or warfarin (W) S/R ratios as a biomarker for CYP2C9 activity.
  109. Effect of sex and menstrual cycle phase on cytochrome P450 2C19 activity with omeprazole used as a biomarker
  110. CYP2D6 Inhibition by Selective Serotonin Reuptake Inhibitors: Analysis of Achievable Steady-State Plasma Concentrations and the Effect of Ultrarapid Metabolism at CYP2D6
  111. Unique CYP2D6 activity distribution and genotype-phenotype discordance in black Americans*
  112. Concordance between Tramadol and Dextromethorphan Parent/Metabolite Ratios: The Influence of CYP2D6 and Non-CYP2D6 Pathways on Biotransformation
  113. Cytochrome P4502C9 (CYP2C9) allele frequencies in Canadian Native Indian and Inuit populations
  114. Effects of Oral Vitamin K on S- and R-Warfarin Pharmacokinetics and Pharmacodynamics: Enhanced Safety of Warfarin as a CYP2C9 Probe
  115. Cytochrome P4502C9 (CYP2C9) allele frequencies in Canadian Native Indian and Inuit populations
  116. Interethnic differences of drug-metabolizing enzymes
  117. Optimization of cytochrome P4502D6 (CYP2D6) phenotype assignment using a genotyping algorithm based on allele frequency data
  118. Optimization of cytochrome P4502D6 (CYP2D6) phenotype assignment using a genotyping algorithm based on allele frequency data
  119. Dose dependency of dextromethorphan for cytochrome P450 2D6 (CYP2D6) phenotyping
  120. Crystal structure of human catecholamine sulfotransferase 1 1Edited by R. Huber
  121. Accuracy of cytochrome P4502D6 (CYP2D6): Phenotype assignment from genotyping data1
  122. Acquistion of functional CYP2D6 activity in the first year of life1
  123. Absence of dose-dependency for CYP2D6 phenotyping (PT) with dextromethorphan (DM)
  124. CYP2D6 allele frequencies in African Americans: Phenotype concordance with dextromethorphan (DM)
  125. CYP2C9 genotype and ibuprofen (IBU) pharmacokinetics (PK) in cystic fibrosis (CF)1
  126. Determinants of warfarin S:R ratio in orthopedic surgery (OS) patients
  127. Structural characterization of human aryl sulphotransferases
  128. Structural characterization of human aryl sulphotransferases
  129. Quantification of intraindividual variability and the influence of menstrual cycle phase on CYP2D6 activity as measured by dextromethorphan phenotyping
  130. Comparison of three CYP2D6 probe substrates and genotype in Ghanaians, Chinese and Caucasians
  131. NAD(P)H:quinone oxidoreductase: polymorphisms and allele frequencies in Caucasian, Chinese and Canadian Native Indian and Inuit populations
  132. Non-monooxygenase cytochromes P450 as potential human autoantigens in anticonvulsant hypersensitivity reactions
  133. Chiral phase analysis of warfarin enantiomers in patient plasma in relation to CYP2C9 genotype
  134. Assessment of the predictive power of genotypes for the in-vivo catalytic function of CYP2D6 in a German population
  135. Bacterial expression of two human aryl sulfotransferases
  136. Novel sulfotransferases cloned by RT-PCR: real proteins or PCR artifacts?
  137. Tissue-Specific Expression and Alternative Splicing of Human Microsomal Epoxide Hydrolase
  138. Human acetyltransferase polymorphisms
  139. The role of xenobiotic metabolizing enzymes in arylamine toxicity and carcinogenesis: Functional and localization studies
  140. Cloning, Structural Organization, and Chromosomal Mapping of the Human Phenol SulfotransferaseSTP2Gene
  141. Genetic analysis of microsomal epoxide hydrolase in patients with carbamazepine hypersensitivity
  142. Characterization of the microsomal epoxide hydrolase gene in patients with anticonvulsant adverse drug reactions
  143. Debrisoquine/Sparteine Hydroxylation Genotype and Phenotype: Analysis of Common Mutations and Alleles of CYP2D6 in a European Population
  144. Identification of the primary gene defect at the cytochrome P450 CYP2D locus
  145. Faculty of 1000 evaluation for Children, biobanks and the scope of parental consent.
  146. Faculty of 1000 evaluation for Clinical assessment incorporating a personal genome.
  147. Faculty of 1000 evaluation for Pharmacogenomics of human uridine diphospho-glucuronosyltransferases and clinical implications.
  148. Faculty of 1000 evaluation for The missing association: sequencing-based discovery of novel SNPs in VKORC1 and CYP2C9 that affect warfarin dose in African Americans.
  149. Faculty of 1000 evaluation for A genome-wide association study of metabolic traits in human urine.
  150. Faculty of 1000 evaluation for Functional characterization of liver enhancers that regulate drug-associated transporters.
  151. Faculty of 1000 evaluation for Glycine and a glycine dehydrogenase (GLDC) SNP as citalopram/escitalopram response biomarkers in depression: pharmacometabolomics-informed pharmacogenomics.
  152. Faculty of 1000 evaluation for A genome-wide study identifies HLA alleles associated with lumiracoxib-related liver injury.
  153. Faculty of 1000 evaluation for Predicting adverse drug reactions using publicly available PubChem BioAssay data.
  154. Faculty of 1000 evaluation for [CONFERENCE POSTER]: Intestinal CYP3A4 and midazolam disposition in vivo show seasonal variation and associate with VDR polymorphisms.
  155. Faculty of 1000 evaluation for Neuroimaging in psychiatric pharmacogenetics research: the promise and pitfalls.
  156. Faculty of 1000 evaluation for [CONFERENCE POSTER]: Exploratory analysis of 1936 SNPs in ADME genes for association with busulfan clearance in adult hematopoietic stem cell recipients.