Christopher E. Nelson

The paper shows that exercise preconditioning enhances skeletal muscle hypertrophy through epigenetic and metabolic changes, specifically involving Smox and Wnt signaling.

This study uses long-read sequencing to analyze genomic and transcriptomic changes in AAV-CRISPR therapy for DMD, revealing complex editing outcomes and developing new methods for detection.

This paper develops a standardized, cost-effective microfluidic LNP synthesis protocol with reproducible results across user groups and lipid types.

The paper develops a dual-fluorescence assay to screen gene delivery vehicles in macrophages using an inflammation-inducible reporter, showing divergent effects of different delivery methods.

This study evaluates CRISPR-based gene integration in skeletal muscle using two high-expressing loci, demonstrating high-level therapeutic gene expression in mouse myoblasts.