Philip Belgrader

A comprehensive study on the isolation and characterization of the HeLa S3 nuclear matrix.

[Proteins bound to satellite DNA, are present in human nuclear matrix cell preparations].

Molecular cloning of matrin 3. A 125-kilodalton protein of the nuclear matrix contains an extensive acidic domain.

Automated DNA purification and amplification from blood-stained cards using a robotic workstation.

Mammalian nonsense codons can be cis effectors of nuclear mRNA half-life.

Introns are cis effectors of the nonsense-codon-mediated reduction in nuclear mRNA abundance.

Nonsense but not missense mutations can decrease the abundance of nuclear mRNA for the mouse major urinary protein, while both types of mutations can facilitate exon skipping.

Evidence to implicate translation by ribosomes in the mechanism by which nonsense codons reduce the nuclear level of human triosephosphate isomerase mRNA.

PCR-based human leukocyte antigen (HLA) DQ alpha typing of blood stained light and dark blue denim fabric.

Reusing the same blood-stained punch for sequential DNA amplifications and typing.

Peptide nucleic acid characterization by MALDI-TOF mass spectrometry.

Automated polymerase chain reaction product sample preparation for capillary electrophoresis analysis.

Characterization of mitochondrial DNA using low-stringency single specific primer amplification analyzed by laser induced fluorescence--capillary electrophoresis.

The evaluation of fast purification methods for preparing polymerase chain reaction (PCR) products for capillary electrophoresis analysis.

DNA typing in thirty seconds with a microfabricated device.

Analysis of short tandem repeat polymorphisms in human DNA by matrix-assisted laser desorption/ionization mass spectrometry.

Discrimination of single-nucleotide polymorphisms in human DNA using peptide nucleic acid probes detected by MALDI-TOF mass spectrometry.

DNA typing of human leukocyte antigen sequence polymorphisms by peptide nucleic acid probes and MALDI-TOF mass spectrometry.

Rapid PCR for identity testing using a battery-powered miniature thermal cycler.

Real-time microchip PCR for detecting single-base differences in viral and human DNA.

Analysis of DNA fragments from conventional and microfabricated PCR devices using delayed extraction MALDI-TOF mass spectrometry.

Rapid pathogen detection using a microchip PCR array instrument.

PCR detection of bacteria in seven minutes.

A minisonicator to rapidly disrupt bacterial spores for DNA analysis.

Simultaneous detection of TaqMan probes containing Fam and Tamra reporter fluorophores.

A microfluidic cartridge to prepare spores for PCR analysis.

Toward a rapid, integrated, and fully automated DNA diagnostic assay for chlamydia trachomatis and neisseria gonorrhoeae

A battery-powered notebook thermal cycler for rapid multiplex real-time PCR analysis.

Lysing bacterial spores by sonication through a flexible interface in a microfluidic system.

Microchip isoelectric focusing using a miniature scanning detection system.

A reusable flow-through polymerase chain reaction instrument for the continuous monitoring of infectious biological agents.

A plastic, disposable microfluidic flow cell for coupled on-chip PCR and microarray detection of infectious agents.

High-throughput droplet digital PCR system for absolute quantitation of DNA copy number.

Rapid, simple influenza RNA extraction from nasopharyngeal samples.

Droplet Digitalâ„¢ PCR quantitation of HER2 expression in FFPE breast cancer samples.

Droplet Digital PCR Measurement of HER2 Copy Number Alteration in Formalin-Fixed Paraffin-Embedded Breast Carcinoma Tissue.

Detection of Methicillin-Resistant Staphylococcus Aureus by A Duplex Droplet Digital Polymerase Chain Reaction.