J.-K. Heriche

The paper introduces the Image Data Explorer, a web tool for interactive exploration of image-derived data in bioimage analysis.

LOMAR is a software package for comparing SMLM point sets using registration methods and topological data analysis, applied to nuclear pore complex data.

The paper uses 3D super-resolution microscopy and computational methods to map the 3D structure of the Nuclear Pore Complex in human cells, revealing variable conformations of its subunits.

The paper develops a methodology combining breast organoids and light-sheet imaging to track cell fates and finds that small groups of transformed cells form tumors while isolated cells do not.

The paper uses correlative live and super-resolution microscopy to study replication domain structure and dynamics in higher eukaryotes, finding RDs are 150 nm in size with specific spacing and mechanical coupling.

The paper shows that postmitotic nuclear pore assembly occurs through dilation of ER membrane openings, forming transport channels rapidly.