Iain A. Drummond

Endothelial signaling in kidney morphogenesis: a role for hemodynamic forces.

A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish.

Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination.

Zebrafish kidney development.

Kidney development and disease in the zebrafish.

Cilia-driven fluid flow in the zebrafish pronephros, brain and Kupffer's vesicle is required for normal organogenesis.

roundabout4 is essential for angiogenesis in vivo.

Zebrafish slc4a2/ae2 anion exchanger: cDNA cloning, mapping, functional characterization, and localization.

Organization of the pronephric filtration apparatus in zebrafish requires Nephrin, Podocin and the FERM domain protein Mosaic eyes.

Polycystin-2 immunolocalization and function in zebrafish.

Dynamic expression of the osmosensory channel trpv4 in multiple developing organs in zebrafish.

New functions for a vertebrate Rho guanine nucleotide exchange factor in ciliated epithelia.

Notch signaling controls the differentiation of transporting epithelia and multiciliated cells in the zebrafish pronephros.

The zebrafish fleer gene encodes an essential regulator of cilia tubulin polyglutamylation.

Expression of trpC1 and trpC6 orthologs in zebrafish.

Some assembly required: renal hypodysplasia and the problem with faulty parts.

odd skipped related1 reveals a novel role for endoderm in regulating kidney versus vascular cell fate.

Collective cell migration drives morphogenesis of the kidney nephron.

Cloning, localization, and functional expression of the electrogenic Na+ bicarbonate cotransporter (NBCe1) from zebrafish.

Fluid flow and guidance of collective cell migration.

The ADPKD genes pkd1a/b and pkd2 regulate extracellular matrix formation.

Polyglutamylation and the fleer gene.

Cloning and characterization of a zebrafish homologue of human AQP1: a bifunctional water and gas channel.

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

Zebrafish kidney development.

Tubulin tyrosine ligase-like genes ttll3 and ttll6 maintain zebrafish cilia structure and motility.

Polycystins, focal adhesions and extracellular matrix interactions.

CaMK-II is a PKD2 target that promotes pronephric kidney development and stabilizes cilia.

Cilia functions in development.

Mutation mapping and identification by whole-genome sequencing.

CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms.

Live imaging kidney development in zebrafish.

Mechanical stretch and PI3K signaling link cell migration and proliferation to coordinate epithelial tubule morphogenesis in the zebrafish pronephros.

Inhibitory effects of Robo2 on nephrin: a crosstalk between positive and negative signals regulating podocyte structure.

Invasion of distal nephron precursors associates with tubular interconnection during nephrogenesis.

The cilium in lights: new views of an ancient organelle.

ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6.

odd-skipped related 2 is required for fin chondrogenesis in zebrafish.

Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.

A homozygous PDE6D mutation in Joubert syndrome impairs targeting of farnesylated INPP5E protein to the primary cilium.

A zebrafish model of chordoma initiated by notochord-driven expression of HRASV12.

Modulation of the secretory pathway rescues zebrafish polycystic kidney disease pathology.

osr1 is required for podocyte development downstream of wt1a.

Cytoplasmic carboxypeptidase 5 regulates tubulin glutamylation and zebrafish cilia formation and function.

Collective epithelial migration drives kidney repair after acute injury.

Prostaglandin signalling regulates ciliogenesis by modulating intraflagellar transport.

Odd skipped related 1 is a negative feedback regulator of nodal-induced endoderm development.

Shroom3 contributes to the maintenance of the glomerular filtration barrier integrity.

Nephronophthisis-associated CEP164 regulates cell cycle progression, apoptosis and epithelial-to-mesenchymal transition.

The Lowe syndrome protein OCRL1 is required for endocytosis in the zebrafish pronephric tubule.