Noga Moshe

This study identifies conserved and divergent developmental programs for cerebellar output neurons in zebrafish, showing shared origins with other vertebrates and unique mechanisms for eurydendroid cell organization.

This study identifies potential treatments for Kaposiform Lymphangiomatosis using a zebrafish model and high-throughput drug screening.

This study identifies a conserved venous remodeling program in zebrafish that mirrors mammalian IVC formation, revealing cellular origins and molecular mechanisms of IVC development.

This study identifies endolysosomal dysfunction in radial glia progenitor cells as a cause of defective cerebral angiogenesis and BBB compromise in zebrafish, linking Notch3 processing defects to CSVD phenotypes.

This study creates zebrafish mutants to study Apolipoprotein B's role in development and disease, finding defects in lipid metabolism and vascular development.

This study shows that VEGFC induces cell-cycle arrest in endothelial cells, promoting sprouting and differentiation in venous and lymphatic vessels.

This study shows that lymphatic endothelial cells can transdifferentiate into blood vessel endothelial cells in zebrafish, linking cell origin to function in vascular development and regeneration.