Barely Significant
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XLID syndrome gene Med12 promotes Ig isotype switching through chromatin modification and enhancer RNA regulation.

Sci Adv · 2022 · PMC9699684 · PMID 36427307

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a clear trendno p-value reported
Multiple siMed12 concentrations effectively inhibited CSR with a clear trend of dose dependency ( Fig. 1A and fig S1A).

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