Malfunctions of KLHL6 mutants extended beyond proximal BCR signaling with distinct phenotypes from KLHL6 silencing. Collectively, our findings uncover how recurrent mutations in KLHL6 alter BCR signaling and induce actionable phenotypic characteristics in DLBCL.
almost 2 years ago
Journal
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CD79B (CD79b Molecule) • CD79A (CD79a Molecule) • KLHL6 (Kelch Like Family Member 6)