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Publisher Correction: BAF complex vulnerabilities in cancer demonstrated via structure-based PROTAC design

The Original Article was published on 10 June 2019

Correction to: Nature Chemical Biology, https://doi.org/10.1038/s41589-019-0294-6, published online 10 June 2019

In the version of this article originally published, several lines of text in the last paragraph of the right column on page 1 of the PDF were transposed into the bottom paragraph of the left column. The affected text of the left column should read “The ATP-dependent activities of the BAF (SWI/SNF) chromatin remodeling complexes affect the positioning of nucleosomes on DNA and thereby many cellular processes related to chromatin structure, including transcription, DNA repair and decatenation of chromosomes during mitosis12,13.” The affected text of the right column should read “SMARCA2/4BD inhibitors are thus precluded from use for the treatment of SMARCA4 mutant cancers but could provide attractive ligands for PROTAC conjugation. Small molecules binding to other bromodomains have been successfully converted into PROTACs by conjugating them with structures capable of binding to the E3 ligases von Hippel−Lindau (VHL) or cereblon5,6,10,11,25,26,27.” The errors have been corrected in the PDF version of the paper.

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Correspondence to Darryl B. McConnell or Alessio Ciulli.

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Farnaby, W., Koegl, M., Roy, M.J. et al. Publisher Correction: BAF complex vulnerabilities in cancer demonstrated via structure-based PROTAC design. Nat Chem Biol 15, 846 (2019). https://doi.org/10.1038/s41589-019-0329-z

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