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Cell cycle–dependent localization of the proteasome to chromatin
2020
Scientific Reports
An integrative understanding of nuclear events including transcription in normal and cancer cells requires comprehensive and quantitative measurement of protein dynamics that underlie such events. However, the low abundance of most nuclear proteins hampers their detailed functional characterization. We have now comprehensively quantified the abundance of nuclear proteins with the use of proteomics approaches in both normal and transformed human diploid fibroblasts. We found that subunits of the
doi:10.1038/s41598-020-62697-2
pmid:32242037
fatcat:g7obwsgqpzglrireicfegpq6mm