ereprof. dr. Joël Vandekerckhove
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Combining quantitative proteomics data processing workflows for greater sensitivity
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Proteome-derived peptide libraries allow detailed analysis of the substrate specificities of Nα-acetyltransferases and point to hNaa10p as the post-translational actin Nα-acetyltransferase
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Redox proteomics of protein-bound methionine oxidation
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Gamma-Tubulin localizes at actin-based membrane protrusions and inhibits formation of stress-fibers
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Unconventional actin conformations localize on intermediate filaments in mitosis
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A stringent approach to improve the quality of nitrotyrosine peptide identifications
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A comparison of MS2-based label-free quantitative proteomic techniques with regards to accuracy and precision
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A reproducibility-based evaluation procedure for quantifying the differences between MS/MS peak intensity normalization methods
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Probing the efficiency of proteolytic events by positional proteomics
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Actin and arp2/3 localize at the centrosome of interphase cells