Robert J. Bryson-Richardson

The structure and evolution of the melanocortin and MCH receptors in fish and mammals.

Sequence characterization of teleost fish melanocortin receptors.

Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo.

Cadherin-mediated differential cell adhesion controls slow muscle cell migration in the developing zebrafish myotome.

Large-scale analysis of gene structure in rhodopsin-like GPCRs: evidence for widespread loss of an ancient intron.

Met and Hgf signaling controls hypaxial muscle and lateral line development in the zebrafish.

Developmentally restricted actin-regulatory molecules control morphogenetic cell movements in the zebrafish gastrula.

Optical projection tomography for spatio-temporal analysis in the zebrafish.

Analysis of protein sequence and interaction data for candidate disease gene prediction.

The eIF4G-homolog p97 can activate translation independent of caspase cleavage.

Whole-somite rotation generates muscle progenitor cell compartments in the developing zebrafish embryo.

The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin alpha2-deficient congenital muscular dystrophy.

FishNet: an online database of zebrafish anatomy.

The genetics of vertebrate myogenesis.

The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachment.

Zebrafish prox1b mutants develop a lymphatic vasculature, and prox1b does not specifically mark lymphatic endothelial cells.

Cardiac-phase filtering in intracardiac particle image velocimetry.

Characterization and investigation of zebrafish models of filamin-related myofibrillar myopathy.

The Zebrafish Anatomy Portal: a novel integrated resource to facilitate zebrafish research.

Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy.

In vivo wall shear measurements within the developing zebrafish heart.

The quail anatomy portal.