(Phospho)proteomic Profiling of Microsatellite Unstable CRC Cells Reveals Alterations in Nuclear Signaling and Cholesterol Metabolism Caused by Frameshift Mutation of NMD Regulator UPF3A

DNA mismatch repair-deficient colorectal cancers (CRCs) accumulate quite a few frameshift mutations at repetitive sequences acknowledged as microsatellite instability (MSI). When coding mononucleotide repeats (cMNRs)

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