Real-time fluorescence genotyping of factor V Leiden during rapid-cycle PCR.
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C. Wittwer | C T Wittwer | M J Lay | M. Lay | Marla J. Lay
[1] R. Blasczyk,et al. Simple and Rapid Detection of Factor V Leiden by Allele-specific PCR Amplification , 1996, Thrombosis and Haemostasis.
[2] R. Moreno,et al. DNA extraction with organic solvents in gel barrier tubes. , 1989, Nucleic acids research.
[3] K. Voelkerding,et al. Factor V R506Q gene mutation analysis by PCR-RFLP: optimization, comparison with functional testing for resistance to activated protein C, and establishment of cell line controls. , 1996, American journal of clinical pathology.
[4] Kirk M. Ririe,et al. Fluorescence Monitoring of Rapid Cycle PCR for Quantification , 1998 .
[5] K. Livak,et al. Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization. , 1995, PCR methods and applications.
[6] Sanjay Tyagi,et al. Molecular Beacons: Probes that Fluoresce upon Hybridization , 1996, Nature Biotechnology.
[7] R. Zotz,et al. Mutation in the Gene Coding for Coagulation Factor V and Resistance to Activated Protein C: Detection of the Genetic Mutation by Oligonucleotide Ligation Assay Using a Semi-automated System , 1996, Thrombosis and Haemostasis.
[8] Kirk M. Ririe,et al. Rapid Cycle DNA Amplification , 1994 .
[9] 18 – Detection of Energy Transfer and Fluorescence Quenching , 1995 .
[10] J. Corral,et al. Detection of Factor V Leiden from a Drop of Blood by PCR-SSCP , 1996, Thrombosis and Haemostasis.
[11] B. Eisenstein,et al. The polymerase chain reaction. A new method of using molecular genetics for medical diagnosis. , 1990, The New England journal of medicine.
[12] Kirk M. Ririe,et al. Product differentiation by analysis of DNA melting curves during the polymerase chain reaction. , 1997, Analytical biochemistry.
[13] L. Morrison. 13 – Detection of Energy Transfer and Fluorescence Quenching , 1992 .
[14] T. Goodman,et al. Salt dependence and thermodynamic interpretation of the thermal denaturation of small DNA restriction fragments. , 1981, Nucleic Acids Research.
[15] J. Shaffer,et al. Hybridization of synthetic oligodeoxyribonucleotides to ΦX 174 DNA: the effect of single base pair mismatch , 1979 .
[16] J. Clegg,et al. Evidence for a single origin of factor V Leiden , 1996, British journal of haematology.
[17] D. Seligson,et al. Clinical Chemistry , 1965, Bulletin de la Societe de chimie biologique.
[18] Lloyd M. Smith,et al. Enhanced discrimination of single nucleotide polymorphisms by artificial mismatch hybridization , 1997, Nature Biotechnology.
[19] K. Itakura,et al. Dissociation kinetics of 19 base paired oligonucleotide-DNA duplexes containing different single mismatched base pairs. , 1987, Nucleic acids research.
[20] H. Liebman,et al. Evaluation of a tissue factor dependent factor V assay to detect factor V Leiden: demonstration of high sensitivity and specificity for a generally applicable assay for activated protein C resistance , 1996, British journal of haematology.
[21] R. Horton,et al. Genetic Engineering with PCR , 1998 .
[22] J. Bidwell,et al. Genetic Diagnosis of Factor V Leiden Using Heteroduplex Technology , 1997, Thrombosis and Haemostasis.
[23] J. Voorberg,et al. Association of idiopathic venous thromboembolism with single point-mutation at Arg506 of factor V , 1994, The Lancet.
[24] U J Balis,et al. The LightCycler: a microvolume multisample fluorimeter with rapid temperature control. , 1997, BioTechniques.
[25] C. Wittwer,et al. Continuous fluorescence monitoring of rapid cycle DNA amplification. , 1997, BioTechniques.
[26] Pieter H. Reitsma,et al. Mutation in blood coagulation factor V associated with resistance to activated protein C , 1994, Nature.