Alan J. Davidson

Wnt8a expands the pool of embryonic kidney progenitors in zebrafish.

Neuropilin-1 is required for vascular development and is a mediator of VEGF-dependent angiogenesis in zebrafish.

Radar is required for the establishment of vascular integrity in the zebrafish.

Biomedicine. Love, honor, and protect (your liver).

Cell-specific mitotic defect and dyserythropoiesis associated with erythroid band 3 deficiency.

Inhibition of zebrafish epidermal growth factor receptor activity results in cardiovascular defects.

cdx4 mutants fail to specify blood progenitors and can be rescued by multiple hox genes.

Expression and mapping of duplicate neuropilin-1 and neuropilin-2 genes in developing zebrafish.

The 'definitive' (and 'primitive') guide to zebrafish hematopoiesis.

An Mll-dependent Hox program drives hematopoietic progenitor expansion.

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

Zebrafish scl functions independently in hematopoietic and endothelial development.

Regulation of the lmo2 promoter during hematopoietic and vascular development in zebrafish.

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

The caudal-related homeobox genes cdx1a and cdx4 act redundantly to regulate hox gene expression and the formation of putative hematopoietic stem cells during zebrafish embryogenesis.

Sustained Bmp signaling is essential for cloaca development in zebrafish.

Cdx4 dysregulates Hox gene expression and generates acute myeloid leukemia alone and in cooperation with Meis1a in a murine model.

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

BMP and Wnt specify hematopoietic fate by activation of the Cdx-Hox pathway.

montalcino, A zebrafish model for variegate porphyria.

Intestinal differentiation in zebrafish requires Cdx1b, a functional equivalent of mammalian Cdx2.

Pseudomonas aeruginosa infection of zebrafish involves both host and pathogen determinants.

The role and regulation of friend of GATA-1 (FOG-1) during blood development in the zebrafish.

Interaction of retinoic acid and scl controls primitive blood development.

Zebrafish wnt9a is expressed in pharyngeal ectoderm and is required for palate and lower jaw development.

Zebrafish kidney development.

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

Uncharted waters: nephrogenesis and renal regeneration in fish and mammals.

Interactions between Cdx genes and retinoic acid modulate early cardiogenesis.

Zebrafish kidney development: basic science to translational research.

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.

HNF1β is essential for nephron segmentation during nephrogenesis.

A zebrafish model of conditional targeted podocyte ablation and regeneration.

Histone deacetylase inhibitor enhances recovery after AKI.

Kidney regeneration: common themes from the embryo to the adult.

Hnf1beta and nephron segmentation.

A Cdx4-Sall4 regulatory module controls the transition from mesoderm formation to embryonic hematopoiesis.

Kidney regeneration in fish.

Kidney injury and regeneration in zebrafish.

The small molecule probe PT-Yellow labels the renal proximal tubules in zebrafish.

Pronephric tubule formation in zebrafish: morphogenesis and migration.

BMP and retinoic acid regulate anterior-posterior patterning of the non-axial mesoderm across the dorsal-ventral axis.

Caudal migration and proliferation of renal progenitors regulates early nephron segment size in zebrafish.

Derivation of Corneal Keratocyte-Like Cells from Human Induced Pluripotent Stem Cells.

The Vital Dye CDr10b Labels the Zebrafish Mid-Intestine and Lumen.

Zebrafish Pronephros Development.

The zebrafish kidney mutant zeppelin reveals that brca2/fancd1 is essential for pronephros development.

The role of macrophages during acute kidney injury: destruction and repair.

Transgenic Xenopus laevis Line for In Vivo Labeling of Nephrons within the Kidney.

A Simple Bioreactor-Based Method to Generate Kidney Organoids from Pluripotent Stem Cells.

Turning mesoderm into kidney.

A novel mechanism of gland formation in zebrafish involving transdifferentiation of renal epithelial cells and live cell extrusion.

Enhancing regeneration after acute kidney injury by promoting cellular dedifferentiation in zebrafish.

Mind the gap: renal tubule responses to injury and the role of Cxcl12 and Myc.

Transcriptional profiling of the zebrafish proximal tubule.

Evaluation of cisplatin-induced injury in human kidney organoids.

Use of Human Induced Pluripotent Stem Cells and Kidney Organoids To Develop a Cysteamine/mTOR Inhibition Combination Therapy for Cystinosis.

The Utility of Human Kidney Organoids in Modeling Kidney Disease.

Common Variants Coregulate Expression of GBA and Modifier Genes to Delay Parkinson's Disease Onset.

ADAM10 mediates ectopic proximal tubule development and renal fibrosis through Notch signalling.

SOX9 promotes stress-responsive transcription of VGF nerve growth factor inducible gene in renal tubular epithelial cells.

Protocol for Large-Scale Production of Kidney Organoids from Human Pluripotent Stem Cells.

Human Urinal Cell Reprogramming: Synthetic 3D Peptide Hydrogels Enhance Induced Pluripotent Stem Cell Population Homogeneity.

The Dynamics of Metabolic Characterization in iPSC-Derived Kidney Organoid Differentiation a Comparative Omics Approach.