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Single Nucleotide Polymorphisms as Genomic Markers for High-Throughput Pharmacogenomic Studies.
Lonetti, Annalisa; Fontana, Maria Chiara; Martinelli, Giovanni; Iacobucci, Ilaria.
Afiliação
  • Lonetti A; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
  • Fontana MC; Department of Experimental, Diagnostic and Specialty Medicine, Institute of Hematology "L. and A. Seràgnoli", University of Bologna, Via Massarenti, 9, Bologna, 40138, Italy.
  • Martinelli G; Department of Experimental, Diagnostic and Specialty Medicine, Institute of Hematology "L. and A. Seràgnoli", University of Bologna, Via Massarenti, 9, Bologna, 40138, Italy.
  • Iacobucci I; Department of Experimental, Diagnostic and Specialty Medicine, Institute of Hematology "L. and A. Seràgnoli", University of Bologna, Via Massarenti, 9, Bologna, 40138, Italy. ilaria.iacobucci2@unibo.it.
Methods Mol Biol ; 1368: 143-59, 2016.
Article em En | MEDLINE | ID: mdl-26614074
ABSTRACT
Genetic variations in patients have strong impact on their drug therapies and responses because the variations may contribute to the efficacy and/or produce undesirable side effects for any given drug. The Drug Metabolizing Enzymes and Transporters (DMET) assay is a high-throughput technology by Affymetrix that is able to simultaneously genotype variants in multiple genes involved in absorption, distribution, metabolism, and excretion of drugs for subsequent clinical applications, i.e., the assay allows for a precise genetic map that can guide therapeutic interventions and avoid side effects.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Farmacogenética / Polimorfismo de Nucleotídeo Único Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Farmacogenética / Polimorfismo de Nucleotídeo Único Idioma: En Ano de publicação: 2016 Tipo de documento: Article