Feng‐Xia Liang

This study identifies oncostatin M-driven vascular leak in human endothelial cells through nanoscale channel formation, distinct from junction disassembly, and highlights potential therapeutic targets.

SnapG automates g-ratio measurement from electron micrographs, providing accurate and reproducible results with batch processing capabilities.

This study identifies DeSI1 as a cyclin D-CDK4/6 substrate whose phosphorylation regulates membrane and mitochondrial protein supply during proliferation.

This study shows that loss of PKP2 in cardiomyocytes induces pro-inflammatory senescence in non-myocytes and premature cardiac aging, linking desmosomal arrhythmogenic cardiomyopathy to cellular senescence and aging mechanisms.

The paper uses CRISPR D-BUGS and chromosome swapping to identify and resolve genetic interactions in synthetic chromosomes, revealing unexpected links between transcription, inositol metabolism, and tRNA abundance.

The paper segments and quantifies axonal dispersion and diameter in mouse brain corpus callosum using electron microscopy and a semi-automatic algorithm, showing orientation metrics are time-independent while diameter depends on MRI settings.