James Marks

This study identifies FASN's RNA binding sites and shows its depletion reduces translational efficiency of associated mRNAs.

The paper quantifies disome levels across the transcriptome in yeast and human cells under basal and stress conditions, showing stress-induced increases and context-dependent redistribution.

This study shows 5-AzaC incorporation into mRNAs disrupts translation, causes ribosome collisions, and activates stress responses, contributing to its cytotoxicity beyond DNA hypomethylation.

This study investigates how antibiotics inhibit mitochondrial translation, finding that most act similarly to their bacterial targets and identifying errors in annotated mitochondrial translation initiation sites.

The paper uses retapamulin-assisted ribosome profiling to identify alternative translation start sites in E. coli, revealing new proteins and regulatory roles.