P. Gönczy

The paper investigates centriole elimination during C. elegans oogenesis, identifying SAS-1 as a key protein involved in the initial loss of centriole structure.

The paper uses simulations to study SAS-6 ring self-assembly on surfaces, finding that weak interactions and small angular ranges favor nine-fold symmetry.

This study uses advanced imaging techniques to reveal the detailed molecular architecture of the C. elegans centriole and its assembly mechanisms.

The paper examines microtubule symmetry in the centriole and axoneme of Lecudina tuzetae, finding that a 6- or 5-fold axonemal symmetry is paired with an 8-fold centriolar symmetry, indicating plasticity in the transition between these structures.

The paper shows that unequal cell division in C. elegans embryos is essential for successful development, as equalizing cell sizes leads to developmental defects.

This study identifies two physical principles governing centriole formation through surface-catalyzed SAS-6 self-assembly and structural conversion.

This study identifies TRIM37's role in preventing centriolar protein assembly by stabilizing Centrobin, which is critical for maintaining genome integrity in Mulibrey nanism.

The paper uses cryo-tomography and sub-tomogram averaging to reveal novel features of centriole polarity and cartwheel stacking in flagellates.