Lilianna Solnica‐Krezel

This study identifies a zebrafish mutation in ddx49 causing differential cell-type vulnerability in pigment cells due to impaired ribosome biogenesis.

This study investigates the role of Dachsous cadherins in regulating the yolk microtubule and actin cytoskeleton during zebrafish epiboly, showing their necessity for microtubule dynamics and cytoskeletal organization.

This study identifies sox2+ progenitors as critical for zebrafish spinal cord regeneration and shows Bach1 transcription factors regulate their activation and quiescence.

The paper identifies a gene involved in pigment cell communication that governs color pattern formation in zebrafish and anemonefish.

The paper identifies dendritic atoh1a+ cells as transient intermediates in zebrafish Merkel cell development and regeneration, showing their role in morphology acquisition through actin remodeling and Ectodysplasin A signaling.

This study identifies CXCR3-CXCL11 signaling as a regulator of endothelial cell angiogenesis and pericyte recruitment during development.

This study identifies inppl1a as a gene regulating cell expansion in zebrafish notochord, spine morphogenesis, and endochondral bone lengthening, revealing a conserved mechanism across species.

This study identifies VPS13B's localization at the cis-trans Golgi interface and shows its functional interaction with FAM177A1 in lipid transport and Golgi dynamics.

This study shows that CARMIL3 is essential for endodermal cell migration and morphogenesis during zebrafish embryogenesis, affecting Kupffer's vesicle formation and left/right asymmetry.

This study identifies mutations affecting spine development in zebrafish, revealing new candidate genes for human spine disorders like scoliosis.

This study profiles transcriptional and morphogenetic features of human gastruloids, identifying seven cell types and conserved sorting behaviors during embryogenesis.

This study shows Nodal signaling promotes convergence & extension movements in zebrafish neuroectoderm independently of mesoderm, through cell-autonomous effects on mediolateral polarization.

This study shows that the Reissner fiber, secreted by the subcomissural organ in zebrafish, is essential for spine morphogenesis and its loss leads to scoliosis.

This study identifies Gon4l's role in zebrafish gastrulation by regulating mediolateral cell polarity and notochord boundary formation through modulation of cell adhesion molecules.