Integrated amplification and detection of the C677T point mutation in the methylenetetrahydrofolate reductase gene by fluorescence resonance energy transfer and probe melting curves

Analytical Biochemistry

Volumn 255, Issue 1, 1998, Pages 101-107

  Bernard, Philip S ^a   Lay, Marla J ^b   Wittwer, Carl T ^a  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b ARUP INSTITUTE FOR CLINICAL AND EXPERIMENTAL PATHOLOGY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; ELECTROPHORESIS; ENERGY TRANSFER; FORSTER RESONANCE ENERGY TRANSFER; GENES; IMAGE SEGMENTATION; MELTING; RESONANCE;

ASYMMETRIC AMPLIFICATION; FLUORESCENCE METHOD; FLUORESCENCE RESONANCE ENERGY TRANSFER; METHYLENETETRAHYDROFOLATE REDUCTASE GENE; RESONANCE ENERGY TRANSFER; SINGLE-BASE MISMATCH; TEMPERATURE INCREASE; WATSON-CRICK PAIRING;

PROBES;

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); GENE PRODUCT;

AMINO ACID METABOLISM; ARTICLE; BASE MISPAIRING; ENERGY TRANSFER; FLUORESCENCE; GENOTYPE; HYPERHOMOCYSTEINEMIA; NEURAL TUBE DEFECT; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; THROMBOEMBOLISM;

EID: 0031984605     PISSN: 00032697     EISSN: None     Source Type: Journal    
DOI: 10.1006/abio.1997.2427     Document Type: Article

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