G. Pont-Kingdon

发表

A Novel Intron Element Operates Posttranscriptionally To Regulate Human N-mycExpression

G. Mayr, W. Carroll, K. Le, 1999, Molecular and Cellular Biology.

Expression myc N-Posttranscriptionally To Regulate Human A Novel Intron Element Operates

Gabriele, Mayr, W. Carroll, 1998 .

Processed Pseudogene Confounding Deletion/Duplication Assays for SMAD4.

E. Lyon, P. Bayrak-Toydemir, C. Gau, 2015, The Journal of molecular diagnostics : JMD.

Multiplex genotyping by melting analysis of loci-spanning probes: beta-globin as an example.

E. Lyon, M. Herrmann, M. Erali, 2007, BioTechniques.

Sickle cell disease resulting from uniparental disomy in a child who inherited sickle cell trait.

E. Lyon, J. Swensen, J. Prchal, 2010, Blood.

Unlabeled oligonucleotides as internal temperature controls for genotyping by amplicon melting.

E. Lyon, K. Voelkerding, J. Durtschi, 2007, The Journal of molecular diagnostics : JMD.

Validation of an unlabeled probe melting analysis assay combined with high-throughput extractions for genotyping of the most common variants in HFE-associated hereditary hemochromatosis, C282Y, H63D, and S65C.

E. Lyon, S. Dobrowolski, Cindy Meadows, 2012, Genetic testing and molecular biomarkers.

DNA variant databases improve test accuracy and phenotype prediction in Alport syndrome

Jie Ding, D. Crockett, R. Cotton, 2014, Pediatric Nephrology.

Molecular testing for adult type Alport syndrome

E. Lyon, M. Gregory, G. Pont-Kingdon, 2009, BMC nephrology.

Simultaneous amplification, detection, and analysis of common mutations in the galactose-1-phosphate uridyl transferase gene.

E. Lyon, R. Mao, Lesa M Nelson, 2007, The Journal of molecular diagnostics : JMD.

RNA expression from a site-specific non-LTR retrotransposon microinjected into Xenopus oocytes

S. Christensen, D. Carroll, E. Chi, 2004, Genetica.

Mitochondrial Genomes of Anthozoa (Cnidaria)

R. Okimoto, D. Wolstenholme, J. Macfarlane, 1995 .

Direct molecular haplotyping by melting curve analysis of hybridization probes: beta 2-adrenergic receptor haplotypes as an example

E. Lyon, G. Pont-Kingdon, 2005, Nucleic acids research.

Mitochondrial DNA of the sea anemone, Metridium senile (Cnidaria): Prokaryote-like genes for tRNAf-Met and small-subunit ribosomal RNA, and standard genetic code specificities for AGR and ATA codons

R. Okimoto, D. Wolstenholme, G. Pont-Kingdon, 1994, Journal of Molecular Evolution.

Definition of the Human N-myc Promoter Region during Development in a Transgenic Mouse Model

S. Rogers, W. Carroll, G. Pont-Kingdon, 1999, Pediatric Research.

Long-range (17.7 kb) allele-specific polymerase chain reaction method for direct haplotyping of R117H and IVS-8 mutations of the cystic fibrosis transmembrane regulator gene.

E. Lyon, Christine Miller, G. Pont-Kingdon, 2004, The Journal of molecular diagnostics : JMD.

Target Specificity of the Endonuclease from theXenopus laevis Non-Long Terminal Repeat Retrotransposon, Tx1L

S. Christensen, D. Carroll, G. Pont-Kingdon, 2000, Molecular and Cellular Biology.

Mitochondrial DNA of Hydra attenuata (Cnidaria): A Sequence That Includes an End of One Linear Molecule and the Genes for l-rRNA, tRNAf-Met, tRNATrp, COII, and ATPase8

R. Okimoto, D. Wolstenholme, R. Warrior, 2000, Journal of Molecular Evolution.

A coral mitochondrial mutS gene

T. Cavalier-smith, D. Wolstenholme, G. D. Clark-Walker, 1995, Nature.

Rapid detection of aneuploidy (trisomy 21) by allele quantification combined with melting curves analysis of single-nucleotide polymorphism loci.

E. Lyon, G. Pont-Kingdon, 2003, Clinical chemistry.

Verification of multiplex ligation-dependent probe amplification probes in the absence of positive samples.

E. Lyon, P. Bayrak-Toydemir, C. Vaughn, 2011, Genetic testing and molecular biomarkers.

Direct molecular haplotyping of the IVS-8 poly(TG) and polyT repeat tracts in the cystic fibrosis gene by melting curve analysis of hybridization probes.

E. Lyon, Sam R Page, G. Pont-Kingdon, 2005, Clinical chemistry.

Characterization of publicly available lymphoblastoid cell lines for disease-associated mutations in 11 genes.

S. Bernacki, F. Schaefer, J. Beck, 2005, Clinical chemistry.

Design and application of noncontinuously binding probes used for haplotyping and genotyping.

E. Lyon, R. Margraf, E. Schütz, 2008, Clinical chemistry.

Lack of association between beta 2‐adrenergic receptor polymorphisms and juvenile idiopathic arthritis

L. Jorde, S. Prahalad, A. Whiting, 2009, Scandinavian journal of rheumatology.

Noncontinuously binding loop-out primers for avoiding problematic DNA sequences in PCR and sanger sequencing.

E. Lyon, J. Swensen, P. Bayrak-Toydemir, 2014, The Journal of molecular diagnostics : JMD.

Design and analytical validation of clinical DNA sequencing assays.

Whitney Wooderchak-Donahue, Pinar Bayrak-Toydemir, Elaine Lyon, 2012, Archives of pathology & laboratory medicine.

The Alport syndrome COL4A5 variant database

Kelli Sumner, Elaine Lyon, Genevieve Pont-Kingdon, 2010, Human mutation.

Construction of chimeric molecules by a two-step recombinant PCR method.

G. Pont-Kingdon, 1994, BioTechniques.

Creation of chimeric junctions, deletions, and insertions by PCR.

Genevieve Pont-Kingdon, G. Pont-Kingdon, 2003, Methods in molecular biology.

Creation of chimeric junctions, deletions, and insertions by PCR.

G. Pont-Kingdon, 1997, Methods in molecular biology.

Comparative studies of the endonucleases from two related Xenopus laevis retrotransposons, Tx1L and Tx2L: target site specificity and evolutionary implications

S. Christensen, D. Carroll, G. Pont-Kingdon, 2004, Genetica.

Trisomy 21 Detected by SNP Allele Ratios

E. Lyon, G. Pont-Kingdon, 2004 .

Intermediates in extrachromosomal homologous recombination in Xenopus laevis oocytes: characterization by electron microscopy.

D. Carroll, G. Pont-Kingdon, R. J. Dawson, 1993, The EMBO journal.