Shawn M. Burgess

Zebrafish foxi one modulates cellular responses to Fgf signaling required for the integrity of ear and jaw patterning.

Transcription start regions in the human genome are favored targets for MLV integration.

Transgenic zebrafish produced by retroviral infection of in vitro-cultured sperm.

Mmm2p, a mitochondrial outer membrane protein required for yeast mitochondrial shape and maintenance of mtDNA nucleoids.

Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR.

Large-scale molecular characterization of adeno-associated virus vector integration in mouse liver.

High-resolution genome-wide mapping of transposon integration in mammals.

Weak palindromic consensus sequences are a common feature found at the integration target sites of many retroviruses.

The zebrafish gene claudinj is essential for normal ear function and important for the formation of the otoliths.

Redefining the common insertion site.

The forkhead transcription factor FoxI1 remains bound to condensed mitotic chromosomes and stably remodels chromatin structure.

The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15.

Efficient genome-wide mutagenesis of zebrafish genes by retroviral insertions.

Species-specific endogenous retroviruses shape the transcriptional network of the human tumor suppressor protein p53.

Expression profiling identifies novel Hh/Gli-regulated genes in developing zebrafish embryos.

Genome wide screens in yeast to identify potential binding sites and target genes of DNA-binding proteins.

Using retroviruses as a mutagenesis tool to explore the zebrafish genome.

Production of pseudotyped retrovirus and the generation of proviral transgenic zebrafish.

Phoenix is required for mechanosensory hair cell regeneration in the zebrafish lateral line.

Molecular dissection of the migrating posterior lateral line primordium during early development in zebrafish.

Sequencing-based expression profiling in zebrafish.

Using a yeast inverse one-hybrid system to identify functional binding sites of transcription factors.

Yeast-based assay identifies novel Shh/Gli target genes in vertebrate development.

Transcriptional signature of accessory cells in the lateral line, using the Tnk1bp1:EGFP transgenic zebrafish line.