Document Detail


The SmartAmp method: Rapid Detection of SNPs in Thiopurine S-Methyltransferase and ABC Transporters ABCC4 and ABCG2.
MedLine Citation:
PMID:  22591349     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
Genetic polymorphisms of drug transporters as well as drug metabolizing enzymes have been documented to play a significant role in patients� responses to medication. A key requirement for advancing personalized medicine is the ability to rapidly and conveniently test for patients� genetic polymorphisms. We have recently developed a rapid and cost-effective method for single nucleotide polymorphism (SNP) detection, named Smart Amplification Process (SmartAmp), which enables us to detect genetic polymorphisms or mutations in 30 to 45 min under isothermal conditions without the need for DNA isolation and PCR amplification. This article presents the SmartAmp-based detection of SNPs in the thiopurine S-methyltransferase gene as well as in the ATP-binding cassette (ABC) transporter ABCC4 and ABCG2 genes that are critically involved in drug-induced adverse reactions. The SmartAmp method is expected to provide a practical and cost-effective tool for pharmacogenomics-based personalized medicine.
Authors:
Wanping Aw; Alexander Lezhava; Akira Andoh; Hiroshi Tanaka; Yoshihide Hayashizaki; Toshihisa Ishikawa
Related Documents :
22633639 - Two novel missense mutations observed in nonketotic hyperglycinemia.
22444929 - Estimation of genetic associations between reproduction and production traits based on ...
22321639 - Lamc1 gene is associated with premature ovarian failure.
22643179 - Meta-analysis of genetic association studies under heterogeneity.
22437649 - Exploring of tri-allelic snps using pyrosequencing and the snapshot methods for forensi...
22914599 - Mutation screening of the apoa5 gene in subjects with coronary artery disease.
24190419 - Variation of isozyme patterns among arachis species.
16827919 - Dna pooling: a comprehensive, multi-stage association analysis of acsl6 and sirt5 polym...
9703429 - Five novel missense mutations of the lewis gene (fut3) in african (xhosa) and caucasian...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2012-5-16
Journal Detail:
Title:  Current drug metabolism     Volume:  -     ISSN:  1875-5453     ISO Abbreviation:  -     Publication Date:  2012 May 
Date Detail:
Created Date:  2012-5-17     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  100960533     Medline TA:  Curr Drug Metab     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Affiliation:
RIKEN Omics Science Center, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama 230-0045, Japan. toshi-i@gsc.riken.jp.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  SNP Web Resources and Their Potential Applications in Personalized Medicine.
Next Document:  Personalized medicine: Potential, barriers and contemporary issues.