Brittania Moodie

This study investigates kinetochore-microtubule interface plasticity in Naegleria by analyzing its kinetochore structure and function, revealing charge-based binding mechanisms that allow sequence divergence.

This study identifies gene targets involved in cell-substrate adhesion through functional genetic analyses in human cells, revealing dynamic requirements and novel regulators.

The paper examines centromere protein dynamics during quiescence entry and exit, showing rapid disassembly and reassembly of centromere proteins with specific timing for CENP-A deposition.

This study investigates the role of the SAC in mitotic timing and error surveillance, finding that Mad2 is dispensable for viability in Cdc20 {Delta}FL cells and that mitotic timing depends on multiple interdependent pathways.

The paper identifies gene targets that modulate sensitivity to anti-microtubule drugs using CRISPR screens in human cells.