Robin Ganesan

This study identifies the ribosome as the activator of angiogenin, revealing how it enhances tRNA cleavage efficiency and ensures substrate specificity through structural rearrangements.

This study examines the effects of PAB1 deletion in yeast on translation initiation, termination, and mRNA decay using RNA-Seq, Ribo-Seq, and mass spectrometry, revealing both direct and indirect consequences.

The paper investigates the timing and nature of Upf1, Upf2, and Upf3 ribosome association during NMD, revealing progressive polysome association and an early Upf1:80S complex.

The paper investigates stop codon readthrough in yeast using ribosome profiling and bioinformatics to identify mRNA features influencing termination efficiency.