Cristina Pujades

The paper shows that progenitor identity determines neuronal synchrony patterns in zebrafish hindbrain development through lineage tracing and functional analysis.

This study identifies Her9's role in maintaining hindbrain boundary cells as proliferative progenitors by inhibiting neurogenesis and promoting symmetric divisions.

The paper identifies heterogeneous dividing progenitors in hindbrain rhombomere centers that rely on Notch3-signaling and exhibit distinct proliferative and neurogenic properties.

The paper introduces DAMAKER, a 3D tool for tracking tissue growth and neuronal differentiation in zebrafish hindbrain over time using in vivo imaging and segmentation.

TEMPO enables sequential genetic labeling and manipulation of vertebrate cell lineages to study birth-order-dependent cell fates.

This study shows that hindbrain boundary cells transition to neurogenic cells through Notch-dependent asymmetric divisions, contributing to neuronal diversity and proportion.

This paper investigates the role of atoh1 genes in zebrafish hindbrain development, showing atoh1a specifies LRL cells and atoh1b drives differentiation, with cell behavior dependent on dorsoventral position.

The paper shows that Yap/Taz-TEAD activity mediates mechanical signal sensing in hindbrain boundary cells, linking mechanical cues to progenitor behavior and cell fate changes.