Improved reliability of allele-specific PCR

BioTechniques

Volumn 33, Issue 3, 2002, Pages 484-490

  Imyanitov, E N ^a   Buslov, K G ^a   Suspitsin, E N ^a   Kuligina, E Sh ^a   Belogubova, E V ^a   Grigoriev, M Yu ^a   Togo, A V ^a   Hanson, K P ^a  

^a N N PETROV RESEARCH INSTITUTE OF ONCOLOGY   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

ACCURACY; ALLELE; ARTICLE; DNA TEMPLATE; GENE AMPLIFICATION; GENE MUTATION; GENETIC POLYMORPHISM; GENETIC VARIABILITY; INSTRUMENTATION; KINETICS; LABORATORY DIAGNOSIS; POLYMERASE CHAIN REACTION; RELIABILITY; SINGLE NUCLEOTIDE POLYMORPHISM; COMPARATIVE STUDY; EVALUATION; GENETICS; METHODOLOGY; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; QUALITY CONTROL; REPRODUCIBILITY; SENSITIVITY AND SPECIFICITY;

COMPLEMENTARY DNA; PRIMER DNA; TUMOR NECROSIS FACTOR ALPHA;

ALLELES; BASE SEQUENCE; DNA PRIMERS; DNA, COMPLEMENTARY; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; QUALITY CONTROL; REPRODUCIBILITY OF RESULTS; SENSITIVITY AND SPECIFICITY; TUMOR NECROSIS FACTOR-ALPHA;

EID: 0036752202     PISSN: 07366205     EISSN: None     Source Type: Journal    
DOI: 10.2144/02333bm04_11841a     Document Type: Article

References (11)

1. Ayyadevara, S., J.J. Thaden, and R.J. Shmookler Reis. 2000. Discrimination of primer 3′-nucleotide mismatch by Taq DNA polymerase during polymerase chain reaction. Anal. Biochem. 284:11-18.
2. Dutton, C. and S.S. Sommer. 1991. Simultaneous detection of multiple single-base alleles at a polymorphic site. BioTechniques 11:700-702.
3. Kristensen, V.N., D. Kelefiotis, T. Kristensen, and A.L. Borresen-Dale. 2001. High-throughput methods for detection of genetic variation. BioTechniques 30:318-332.
4. Malcolm, E.K., G.B. Baber, J.C. Boyd, and M.H. Stoler. 2000. Polymorphism at codon 72 of p53 is not associated with cervical cancer risk. Mod. Pathol. 13:373-378.
5. Mestiri, S., N. Bouaouina, S.B. Ahmed, A. Khedhaier, B.B. Jrad, S. Remadi, and L. Chouchane. 2001. Genetic variation in the tumor necrosis factor-α promoter region and in the stress protein hsp70-2: Susceptibility and prognostic implications in breast carcinoma. Cancer 91:672-678.
6. Orou, A., B. Fechner, G. Utermann, and H.J. Menzel. 1995. Allele-specific competitive blocker PCR: a one-step method with applicability to pool screening. Hum. Mutat. 6:163-169.
7. Parsons, B.L. and R.H. Heflich. 1998. Detection of a mouse H-ras codon 61 mutation using a modified allele-specific competitive blocker PCR genotypic selection method. Mutagenesis 13:581-588.
8. Ravine, D. 1999. Automated mutation analysis. J. Inherit. Metab. Dis. 22:503-518.
9. Sommer, S.S., A.R. Groszbach, and C.D. Bottema. 1992. PCR amplification of specific alleles (PASA) is a general method for rapidly detecting known single-base changes. BioTechniques 12:82-87.
10. Verjans, G.M., B.M. Brinkman, C.E. Van Doornik, A. Kijlstra, and C.L. Verweij. 1994. Polymorphism of tumour necrosis factor-α (TNF-α) at position -308 in relation to ankylosing spondylitis. Clin. Exp. Immunol. 97:45-47.
11. Wu, D.Y., L. Ugozzoli, B.K. Pal, and R.B. Wallace. 1989. Allele-specific enzymatic amplication of β-globin genomic DNA for diagnosis of sickle cell anemia. Proc. Natl. Acad. Sci. USA 86:2757-2760.