D. Whitcombe

发表

Detection of PCR products using self-probing amplicons and fluorescence

D. Whitcombe, J. Theaker, S. P. Guy, 1999, Nature Biotechnology.

Multiplexed assays for detection of mutations in PIK3CA.

M. Ranson, C. Dive, D. Whitcombe, 2008, Clinical chemistry.

Surface enhanced resonance Raman scattering (SERRS)--a first example of its use in multiplex genotyping.

D. Whitcombe, W. Smith, D. Graham, 2001, Chemphyschem : a European journal of chemical physics and physical chemistry.

Advances in approaches to DNA-based diagnostics.

D. Whitcombe, S. Little, C. Newton, 1998, Current opinion in biotechnology.

The elimination of primer-dimer accumulation in PCR.

D. Whitcombe, J. Theaker, S. Little, 1997, Nucleic acids research.

A homogeneous fluorescence assay for PCR amplicons: its application to real-time, single-tube genotyping.

D. Whitcombe, J. Theaker, S. Little, 1998, Clinical chemistry.

Using Scorpion Primers for Genotyping

D. Whitcombe, 2013 .

Target-assembled exciplexes based on Scorpion oligonucleotides.

D. Whitcombe, K. Douglas, E. Bichenkova, 2008, Bioscience reports.

Design and use of scorpions fluorescent signaling molecules.

D. Whitcombe, N. Thelwell, J. Ferguson, 2008, Methods in molecular biology.

* Manuscript Target-assembled exciplexes based on Scorpion oligonucleotides

D. Whitcombe, K. Douglas, A. Gbaj, 2007 .

A homogeneous method for genotyping with fluorescence polarization.

N. J. Gibson, D. Whitcombe, S. Little, 1997, Clinical chemistry.

Assignment of the human ferrochelatase gene (FECH) and a locus for protoporphyria to chromosome 18q22.

N. Carter, D. Albertson, S. J. Smith, 1991, Genomics.

Molecular cloning and characterization of 13 out genes from Erwinia carotovora subspecies carotovora: genes encoding members of a general secretion pathway (GSP) widespread in Gram‐negative bacteria

Denise S Walker, G. Salmond, D. Whitcombe, 1993, Molecular microbiology.

Molecular characterization of a ferrochelatase gene defect causing anomalous RNA splicing in erythropoietic protoporphyria.

D. Whitcombe, T. Cox, R. Sarkany, 1994, The Journal of investigative dermatology.

Molecular analysis of functional and nonfunctional genes for human ferrochelatase: isolation and characterization of a FECH pseudogene and its sublocalization on chromosome 3.

D. Albertson, D. Whitcombe, T. Cox, 1994, Genomics.

Dinucleotide repeat polymorphism at the locus for human ferrochelatase (FECH).

D. Whitcombe, T. Cox, 1993, Human molecular genetics.

ARMS allele-specific amplification-based detection of mutant p53 DNA and mRNA in tumors of the breast.

N. J. Gibson, D. Hodgson, C. Foy, 2001, Clinical chemistry.

Simple multiplex genotyping by surface-enhanced resonance Raman scattering.

Duncan Graham, D. Whitcombe, D. Graham, 2002, Analytical chemistry.