KRAS and BRAF mutations drive distinct chromatin and transcriptional programs
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The CRC Digest
KRAS and BRAF mutations drive distinct chromatin and transcriptional programs
Isogenic cell models revealed that RAS pathway mutations reconfigure chromatin accessibility and modulate WNT signaling, with elevated TCF7L2 expression in BRAF-mutant tumors independently predicting worse overall survival. (Cell Commun Signal)
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