211 related articles for article (PubMed ID: 15163523)
1. Assessment of DHPLC usefulness in the genotyping of GSTP1 exon 5 SNP: comparison to the PCR-RFLP method.
Abbas A; Lepelley M; Lechevrel M; Sichel F
J Biochem Biophys Methods; 2004 May; 59(2):121-6. PubMed ID: 15163523
[TBL] [Abstract][Full Text] [Related]
2. Identification of new single nucleotid polymorphisms (SNP) in alcohol dehydrogenase class IV ADH7 gene within a French population.
Abbas A; Lechevrel M; Sichel F
Arch Toxicol; 2006 Apr; 80(4):201-5. PubMed ID: 16180008
[TBL] [Abstract][Full Text] [Related]
3. Random mutagenesis-PCR to introduce alterations into defined DNA sequences for validation of SNP and mutation detection methods.
Nickerson ML; Warren MB; Zbar B; Schmidt LS
Hum Mutat; 2001 Mar; 17(3):210-9. PubMed ID: 11241843
[TBL] [Abstract][Full Text] [Related]
4. Denaturing high performance liquid chromatography: high throughput mutation screening in familial hypertrophic cardiomyopathy and SNP genotyping in motor neurone disease.
Yu B; Sawyer NA; Caramins M; Yuan ZG; Saunderson RB; Pamphlett R; Richmond DR; Jeremy RW; Trent RJ
J Clin Pathol; 2005 May; 58(5):479-85. PubMed ID: 15858117
[TBL] [Abstract][Full Text] [Related]
5. A comparison of high-resolution melting analysis with denaturing high-performance liquid chromatography for mutation scanning: cystic fibrosis transmembrane conductance regulator gene as a model.
Chou LS; Lyon E; Wittwer CT
Am J Clin Pathol; 2005 Sep; 124(3):330-8. PubMed ID: 16191501
[TBL] [Abstract][Full Text] [Related]
6. Detection of the C282Y and H63D polymorphisms associated with hereditary hemochromatosis using the ABI 7500 fast real time PCR platform.
Tafe LJ; Belloni DR; Tsongalis GJ
Diagn Mol Pathol; 2007 Jun; 16(2):112-5. PubMed ID: 17525682
[TBL] [Abstract][Full Text] [Related]
7. [A new, rapid and robust genotyping method for CYP2C9 and MDR1].
Verstuyft C; Morin S; Yang J; Loriot MA; Barbu V; Kerb R; Brinkmann U; Beaune P; Jaillon P; Becquemont L
Ann Biol Clin (Paris); 2003; 61(3):305-9. PubMed ID: 12805007
[TBL] [Abstract][Full Text] [Related]
8. Comparison of cytochrome P450 2C9 genotyping methods and implications for the clinical laboratory.
Aquilante CL; Lobmeyer MT; Langaee TY; Johnson JA
Pharmacotherapy; 2004 Jun; 24(6):720-6. PubMed ID: 15222661
[TBL] [Abstract][Full Text] [Related]
9. Two-temperature LATE-PCR endpoint genotyping.
Sanchez JA; Abramowitz JD; Salk JJ; Reis AH; Rice JE; Pierce KE; Wangh LJ
BMC Biotechnol; 2006 Dec; 6():44. PubMed ID: 17144924
[TBL] [Abstract][Full Text] [Related]
10. Restriction enzyme analysis of PCR products.
Ota M; Asamura H; Oki T; Sada M
Methods Mol Biol; 2009; 578():405-14. PubMed ID: 19768608
[TBL] [Abstract][Full Text] [Related]
11. Restriction enzyme mining for SNPs in genomes.
Chuang LY; Yang CH; Tsui KH; Cheng YH; Chang PL; Wen CH; Chang HW
Anticancer Res; 2008; 28(4A):2001-7. PubMed ID: 18649739
[TBL] [Abstract][Full Text] [Related]
12. Analysis of human glutathione S-transferase alpha 1 (hGSTA1) gene promoter polymorphism using denaturing high performance liquid chromatography (DHPLC).
Koumaravelou K; Shoaib Z; Adithan C; Charron D; Srivastava A; Tamouza R; Krishnamoorthy R
Clin Chim Acta; 2011 Jul; 412(15-16):1465-8. PubMed ID: 21530499
[TBL] [Abstract][Full Text] [Related]
13. TotalPlex gene amplification using bulging primers for pharmacogenetic analysis of acute lymphoblastic leukemia.
Kang HJ; Oh Y; Chun SM; Seo YJ; Shin HY; Kim CW; Ahn HS; Han BD
Mol Cell Probes; 2008 Jun; 22(3):193-200. PubMed ID: 18385010
[TBL] [Abstract][Full Text] [Related]
14. A high-throughput denaturing high-performance liquid chromatography method for the identification of variant alleles associated with dihydropyrimidine dehydrogenase deficiency.
Ezzeldin H; Okamoto Y; Johnson MR; Diasio RB
Anal Biochem; 2002 Jul; 306(1):63-73. PubMed ID: 12069415
[TBL] [Abstract][Full Text] [Related]
15. Direct sequencing is more accurate and feasible in detecting single nucleotide polymorphisms than RFLP: using human vascular endothelial growth factor gene as a model.
Davis AH; Jianhua Wang ; Tsang TC; Harris DT
Biol Res Nurs; 2007 Oct; 9(2):170-8. PubMed ID: 17909169
[TBL] [Abstract][Full Text] [Related]
16. Single nucleotide polymorphism detection by polymerase chain reaction-restriction fragment length polymorphism.
Ota M; Fukushima H; Kulski JK; Inoko H
Nat Protoc; 2007; 2(11):2857-64. PubMed ID: 18007620
[TBL] [Abstract][Full Text] [Related]
17. High-throughput multiplex single-nucleotide polymorphism analysis for red cell and platelet antigen genotypes.
Denomme GA; Van Oene M
Transfusion; 2005 May; 45(5):660-6. PubMed ID: 15847652
[TBL] [Abstract][Full Text] [Related]
18. Prevalence of the Factor V G1691A and the Factor II/prothrombin G20210A gene polymorphisms among Tamilians.
Angeline T; Bentley HA; Hawk AB; Manners RJ; Mokashi HA; Jeyaraj N; Tsongalis GJ
Exp Mol Pathol; 2005 Aug; 79(1):9-13. PubMed ID: 15896772
[TBL] [Abstract][Full Text] [Related]
19. [Comparison of denaturing high performance liquid chromatography with direct sequencing in the detection of single nucleotide polymorphism].
Shi J; Yang S; Jiang Z; Jiang H; Chen T; Chen Z; Huang W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Jun; 18(3):198-201. PubMed ID: 11402449
[TBL] [Abstract][Full Text] [Related]
20. Genomic organisation of the chicken ghrelin gene and its single nucleotide polymorphisms detected by denaturing high-performance liquid chromatography.
Nie Q; Zeng H; Lei M; Ishag NA; Fang M; Sun B; Yang G; Zhang X
Br Poult Sci; 2004 Oct; 45(5):611-8. PubMed ID: 15623213
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
