Zhaoxia Sun

Insertional mutagenesis in zebrafish rapidly identifies genes essential for early vertebrate development.

Rad9 phosphorylation sites couple Rad53 to the Saccharomyces cerevisiae DNA damage checkpoint.

Identification of 315 genes essential for early zebrafish development.

A genetic screen in zebrafish identifies cilia genes as a principal cause of cystic kidney.

No age-related cell loss in three retinal nuclear layers of the Long-Evans rat.

Cystic kidney gene seahorse regulates cilia-mediated processes and Wnt pathways.

Zebrafish Tsc1 reveals functional interactions between the cilium and the TOR pathway.

Cilia localization is essential for in vivo functions of the Joubert syndrome protein Arl13b/Scorpion.

Chemical modifier screen identifies HDAC inhibitors as suppressors of PKD models.

Intraflagellar transport proteins are essential for cilia formation and for planar cell polarity.

The zebrafish foxj1a transcription factor regulates cilia function in response to injury and epithelial stretch.

Cilia in cell signaling and human disorders.

A cell-based screen for inhibitors of flagella-driven motility in Chlamydomonas reveals a novel modulator of ciliary length and retrograde actin flow.

Analysis of cilia structure and function in zebrafish.

Qilin is essential for cilia assembly and normal kidney development in zebrafish.

The γ-Secretase Cleavage Product of Polycystin-1 Regulates TCF and CHOP-Mediated Transcriptional Activation through a p300-Dependent Mechanism.

Target-of-rapamycin complex 1 (Torc1) signaling modulates cilia size and function through protein synthesis regulation.