H. Ewa Witkowska

Characterization of embryonic globin genes of the zebrafish.

Desorption/ionization on silicon time-of-flight/time-of-flight mass spectrometry.

Head-to-head coiled arrangement of the subunits of the animal fatty acid synthase.

Toward defining the human parotid gland salivary proteome and peptidome: identification and characterization using 2D SDS-PAGE, ultrafiltration, HPLC, and mass spectrometry.

Assessing the effects of diurnal variation on the composition of human parotid saliva: quantitative analysis of native peptides using iTRAQ reagents.

High-molecular-mass APOBEC3G complexes restrict Alu retrotransposition.

Apolipoprotein E*dipalmitoylphosphatidylcholine particles are ellipsoidal in solution.

Octomeric pyruvate-ferredoxin oxidoreductase from Desulfovibrio vulgaris.

The Association of Biomolecular Resource Facilities Proteomics Research Group 2006 study: relative protein quantitation.

A mass spectrometry-based strategy for detecting and characterizing endogenous proteinase activities in complex biological samples.

A "tagless" strategy for identification of stable protein complexes genome-wide by multidimensional orthogonal chromatographic separation and iTRAQ reagent tracking.

The proteomes of human parotid and submandibular/sublingual gland salivas collected as the ductal secretions.

Rapid alterations in cortical protein profiles underlie spontaneous sleep and wake bouts.

Acid-catalyzed oxygen-18 labeling of peptides.

The sodium-hydrogen exchanger NHE1 is an Akt substrate necessary for actin filament reorganization by growth factors.

Survey of large protein complexes in D. vulgaris reveals great structural diversity.

A lectin affinity workflow targeting glycosite-specific, cancer-related carbohydrate structures in trypsin-digested human plasma.

The ABRF Proteomics Research Group studies: educational exercises for qualitative and quantitative proteomic analyses.

ABRF-PRG07: advanced quantitative proteomics study.

Automated iterative MS/MS acquisition: a tool for improving efficiency of protein identification using a LC-MALDI MS workflow.

Evidence-based annotation of transcripts and proteins in the sulfate-reducing bacterium Desulfovibrio vulgaris Hildenborough.

Breaking the bottleneck in the protein biomarker pipeline.

Peptides released by physiological cleavage of semen coagulum proteins form amyloids that enhance HIV infection.

A lectin chromatography/mass spectrometry discovery workflow identifies putative biomarkers of aggressive breast cancers.