Peter D. Currie

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

Dystrophin-deficient zebrafish feature aspects of the Duchenne muscular dystrophy pathology.

Characterization of the laminin gene family and evolution in zebrafish.

Evaluation of exon-skipping strategies for Duchenne muscular dystrophy utilizing dystrophin-deficient zebrafish.

Development and evolution of the muscles of the pelvic fin.

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

A cytochrome p450 conserved in insects is involved in cuticle formation.

Fgf-dependent glial cell bridges facilitate spinal cord regeneration in zebrafish.

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

Quantification of birefringence readily measures the level of muscle damage in zebrafish.

Blockage of lysophosphatidic acid signaling improves spinal cord injury outcomes.

Epistatic dissection of laminin-receptor interactions in dystrophic zebrafish muscle.

A splice site mutation in laminin-α2 results in a severe muscular dystrophy and growth abnormalities in zebrafish.

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

Biasing amacrine subtypes in the Atoh7 lineage through expression of Barhl2.

Zebrafish models flex their muscles to shed light on muscular dystrophies.

Morphogenesis and cell fate determination within the adaxial cell equivalence group of the zebrafish myotome.

Nerve growth factor stimulates cardiac regeneration via cardiomyocyte proliferation in experimental heart failure.

503unc, a small and muscle-specific zebrafish promoter.

A myogenic precursor cell that could contribute to regeneration in zebrafish and its similarity to the satellite cell.

Fgf2 improves functional recovery-decreasing gliosis and increasing radial glia and neural progenitor cells after spinal cord injury.

Loss of Tropomodulin4 in the zebrafish mutant träge causes cytoplasmic rod formation and muscle weakness reminiscent of nemaline myopathy.

Skeletal myogenesis in the zebrafish and its implications for muscle disease modelling.

Analysing regenerative potential in zebrafish models of congenital muscular dystrophy.

Decreased anti-regenerative effects after spinal cord injury in spry4-/- mice.

Novel transgenic lines to label sarcolemma and myofibrils of the musculature.

Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function.

Rapamycin increases neuronal survival, reduces inflammation and astrocyte proliferation after spinal cord injury.

Feedback from each retinal neuron population drives expression of subsequent fate determinant genes without influencing the cell cycle exit timing.

Genetic basis of hindlimb loss in a naturally occurring vertebrate model.

Asymmetric division of clonal muscle stem cells coordinates muscle regeneration in vivo.

Myo18b is essential for sarcomere assembly in fast skeletal muscle.

In vivo expression of Nurr1/Nr4a2a in developing retinal amacrine subtypes in zebrafish Tg(nr4a2a:eGFP) transgenics.

Using Transgenic Zebrafish to Study Muscle Stem/Progenitor Cells.

Stem cell dynamics in muscle regeneration: Insights from live imaging in different animal models.

Muscle Stem Cells Undergo Extensive Clonal Drift during Tissue Growth via Meox1-Mediated Induction of G2 Cell-Cycle Arrest.

Analysis of RNA Expression in Adult Zebrafish Skeletal Muscle.

Phosphorylation of Lbx1 controls lateral myoblast migration into the limb.

In Vivo Function of the Chaperonin TRiC in α-Actin Folding during Sarcomere Assembly.

The Ancient Origins of Neural Substrates for Land Walking.

imaging: shining a light on stem cells in the living animal.

Skeletal malformations of Meox1-deficient zebrafish resemble human Klippel-Feil syndrome.

Fluorescence-Activated Cell Sorting of Larval Zebrafish Muscle Stem/Progenitor Cells Following Skeletal Muscle Injury.

Guidelines and best practices in successfully using Zebrabow for lineage tracing multiple cells within tissues.

Different Fgfs have distinct roles in regulating neurogenesis after spinal cord injury in zebrafish.

RGD inhibition of itgb1 ameliorates laminin-α2-deficient zebrafish fibre pathology.

Muscle precursor cell movements in zebrafish are dynamic and require Six family genes.

The Developmental Phases of Zebrafish Myogenesis.

Stem cells in skeletal muscle growth and regeneration in amniotes and teleosts: Emerging themes.

Effect of Ataluren on dystrophin mutations.

Machine learning discriminates a movement disorder in a zebrafish model of Parkinson's disease.

Integrated Value of Influence: An Integrative Method for the Identification of the Most Influential Nodes within Networks.