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Jacek R. Wisniewski

Researcher at Max Planck Society

Publications -  37
Citations -  4470

Jacek R. Wisniewski is an academic researcher from Max Planck Society. The author has contributed to research in topics: Proteomics & Histone. The author has an hindex of 22, co-authored 37 publications receiving 4163 citations.

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Deep proteome and transcriptome mapping of a human cancer cell line

TL;DR: Comparisons of the proteome and the transcriptome, and analysis of protein complex databases and GO categories, suggest that deep coverage of the functional transcriptome andThe proteome of a single cell type is achieved.
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Integrated Analysis of Protein Composition, Tissue Diversity, and Gene Regulation in Mouse Mitochondria

TL;DR: A proteomic survey of mitochondria from mouse brain, heart, kidney, and liver and combined the results with existing gene annotations produces a list of 591 mitochondrial proteins, including 163 proteins not previously associated with this organelle, which offers new insights into the biogenesis and ancestry of mammalian mitochondria.
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Super-SILAC mix for quantitative proteomics of human tumor tissue

TL;DR: A method to accurately quantify human tumor proteomes is described by combining a mixture of five stable-isotope labeling by amino acids in cell culture (SILAC)-labeled cell lines with human carcinoma tissue, which broadens the scope of SILAC-based proteomics.
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Use of stable isotope labeling by amino acids in cell culture as a spike-in standard in quantitative proteomics

TL;DR: This study describes a different approach—the use of SILAC as an internal or 'spike-in' standard—wherein SILAC is only used to produce heavy labeled reference proteins or proteomes, and the actual experiment is therefore completely decoupled from the labeling procedure.
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Classification of Inhibitors of Hepatic Organic Anion Transporting Polypeptides (OATPs): Influence of Protein Expression on Drug - Drug Interactions

TL;DR: The maximal transport activity (MTA) of each OATP in human liver was predicted from transport kinetics and protein quantification and the effects of a subset of inhibitors on atorvastatin uptake in vivo were predicted.