M Viganò

This paper develops fluorescent protein binders for cell type-specific visualization of endogenous proteins, showing improved signal-to-noise ratio and application in multiple organisms.

This paper develops a light-inducible method to phosphorylate endogenous Myosin and shows it disrupts cytoskeletal dynamics in Drosophila embryos.

The paper develops engineered kinases to specifically phosphorylate fluorescent protein fusions in vivo, demonstrating their use in studying actomyosin activation in Drosophila embryos.

The paper introduces SEED/Harvest, a CRISPR-based method for efficient and controlled knock-in generation in multicellular animals, enabling seamless cassette removal and spatio-temporal protein labeling.