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High-throughput single-cell proteomics quantifies the emergence of macrophage heterogeneity

View ORCID ProfileHarrison Specht, View ORCID ProfileEdward Emmott, David H. Perlman, Antonius Koller, View ORCID ProfileNikolai Slavov
doi: https://doi.org/10.1101/665307
Harrison Specht
1Department of Bioengineering, Northeastern University, Boston, MA 02115, USA
2Barnett Institute, Northeastern University, Boston, MA 02115, USA
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Edward Emmott
1Department of Bioengineering, Northeastern University, Boston, MA 02115, USA
2Barnett Institute, Northeastern University, Boston, MA 02115, USA
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David H. Perlman
1Department of Bioengineering, Northeastern University, Boston, MA 02115, USA
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Antonius Koller
1Department of Bioengineering, Northeastern University, Boston, MA 02115, USA
2Barnett Institute, Northeastern University, Boston, MA 02115, USA
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Nikolai Slavov
1Department of Bioengineering, Northeastern University, Boston, MA 02115, USA
2Barnett Institute, Northeastern University, Boston, MA 02115, USA
3Department of Biology, Northeastern University, Boston, MA 02115, USA
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  • For correspondence: nslavov@alum.mit.edu
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Posted July 09, 2019.
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High-throughput single-cell proteomics quantifies the emergence of macrophage heterogeneity
Harrison Specht, Edward Emmott, David H. Perlman, Antonius Koller, Nikolai Slavov
bioRxiv 665307; doi: https://doi.org/10.1101/665307
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High-throughput single-cell proteomics quantifies the emergence of macrophage heterogeneity
Harrison Specht, Edward Emmott, David H. Perlman, Antonius Koller, Nikolai Slavov
bioRxiv 665307; doi: https://doi.org/10.1101/665307

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