Daniel R. Foltz

This study examines the dynamic interactions between nucleoli and centromeres in living cells, showing that centromeres move and associate with nucleoli during interphase, with these interactions dependent on rDNA transcription and nucleolar integrity.

This study identifies PRPS-PRPSAP complexes as regulators of histone chaperone interactions, linking nucleotide biosynthesis to chromatin assembly.

This study shows replication stress reduces CENP-A nucleosome stability in S phase by disrupting ATRX and DAXX function, leading to centromere instability.

This study identifies CRAMP1 as a selective regulator of histone H1 expression by interacting with GON4L in the histone locus body.

The paper shows FOXM1 and CENP-F coordinately regulate G2/M gene expression, specifically affecting chromosome stability in cancer cells.

This study shows that Lamin A-associated proteins are essential for centromere assembly during mitotic exit by interacting with centromere and kinetochore proteins.

The paper constructs a coessential genetic network to map the dynamic cellular stress response across 625 cancer cell lines, identifying key regulators and modules involved in stress resilience.