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Abstract

<jats:p>&lt;p&gt;Figure S14. TBK1 was deleted using CRISPR/Cas9 in SETD2 WT and SETD2-deficient 786-O cells. Cells were treated with DMSO or 100nM A-1331852 for 72 hours and harvested to assess inflammatory signaling and NOXA expression by immunoblot. Actin was used as a loading control.&lt;/p&gt;</jats:p>

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cells pfigure tbk1 deleted using

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