A Sensitive Fluorescence Anisotropy Method for Point Mutation Detection by Using Core–Shell Fluorescent Nanoparticles and High-Fidelity DNA Ligase
- 5 September 2007
- journal article
- research article
- Published by Wiley in Chemistry – A European Journal
- Vol. 13 (27), 7725-7730
- https://doi.org/10.1002/chem.200700195
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Approaching Real-Time Molecular Diagnostics: Single-Pair Fluorescence Resonance Energy Transfer (spFRET) Detection for the Analysis of Low Abundant Point Mutations in K-ras OncogenesJournal of the American Chemical Society, 2003
- A map of human genome sequence variation containing 1.42 million single nucleotide polymorphismsNature, 2001
- Strategies for Mutational Analysis of the Large Multiexon ATM Gene Using High-Density Oligonucleotide ArraysGenome Research, 1998
- High level multiplex genotyping by MALDI-TOF mass spectrometryNature Biotechnology, 1998
- Large-Scale Identification, Mapping, and Genotyping of Single-Nucleotide Polymorphisms in the Human GenomeScience, 1998
- Template-directed dye-terminator incorporation (TDI) assay: a homogeneous DNA diagnostic method based on fluorescence resonance energy transferNucleic Acids Research, 1997
- Single-well genotyping of diallelic sequence variations by a two-color ELISA-based oligonucleotide ligation assayNucleic Acids Research, 1996
- Towards fully automated genome–wide polymorphism screeningNature Genetics, 1995
- Genetic disease detection and DNA amplification using cloned thermostable ligase.Proceedings of the National Academy of Sciences, 1991
- A Ligase-Mediated Gene Detection TechniqueScience, 1988