Eric C. Schirmer

This study identifies Nup153 as a docking point for splicing machinery at the nuclear pore, showing its role in mRNA processing and gene splicing.

This study identifies altered metabolic, fibrotic, and splicing pathways in EDMD patients through RNA-Seq and pathway analysis, revealing subgroup distinctions and potential biomarkers.

The paper investigates how changes in lamina-associated domains during T-cell activation affect genome organization and gene regulation.

This study identifies host vesicle fusion proteins VAPB, Rab11b, and Rab18 as critical for HSV-1 nuclear egress by facilitating membrane fusion during viral particle egress.