Rebecca A. Wingert

The chianti zebrafish mutant provides a model for erythroid-specific disruption of transferrin receptor 1.

Loss of gata1 but not gata2 converts erythropoiesis to myelopoiesis in zebrafish embryos.

Deficiency of glutaredoxin 5 reveals Fe-S clusters are required for vertebrate haem synthesis.

Mitoferrin is essential for erythroid iron assimilation.

The cdx genes and retinoic acid control the positioning and segmentation of the zebrafish pronephros.

Combinatorial regulation of novel erythroid gene expression in zebrafish.

montalcino, A zebrafish model for variegate porphyria.

Transferrin-a modulates hepcidin expression in zebrafish embryos.

Identification of adult nephron progenitors capable of kidney regeneration in zebrafish.

Zebrafish nephrogenesis involves dynamic spatiotemporal expression changes in renal progenitors and essential signals from retinoic acid and irx3b.

Wt1a, Foxc1a, and the Notch mediator Rbpj physically interact and regulate the formation of podocytes in zebrafish.

Renal stem cells: fact or science fiction?

Regenerative medicine for the kidney: stem cell prospects & challenges.

Kidney organogenesis in the zebrafish: insights into vertebrate nephrogenesis and regeneration.

New tides: using zebrafish to study renal regeneration.

Knockdown of SCF(Skp2) function causes double-parked accumulation in the nucleus and DNA re-replication in Drosophila plasmatocytes.

Zebrafish nephrogenesis is regulated by interactions between retinoic acid, mecom, and Notch signaling.

Congenital and Acute Kidney Disease: Translational Research Insights from Zebrafish Chemical Genetics.

Roles of Iroquois Transcription Factors in Kidney Development.

Using zebrafish to study podocyte genesis during kidney development and regeneration.