about
Development and evolution of the muscles of the pelvic finThe zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin alpha2-deficient congenital muscular dystrophy.The evolutionary history of the development of the pelvic fin/hindlimbA splice site mutation in laminin-α2 results in a severe muscular dystrophy and growth abnormalities in zebrafishMorphogenesis and cell fate determination within the adaxial cell equivalence group of the zebrafish myotomeDevelopment of the Synarcual in the Elephant Sharks (Holocephali; Chondrichthyes): Implications for Vertebral Formation and FusionShaping muscle bioarchitecture for the fin to limb transitionMorphogenesis and evolution of vertebrate appendicular muscleControl of morphogenetic cell movements in the early zebrafish myotome.The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachmentZebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle functionIsolation of three zebrafish dachshund homologues and their expression in sensory organs, the central nervous system and pectoral fin buds.FishNet: an online database of zebrafish anatomy.The role of zebrafish in chemical genetics.Fate bias during neural regeneration adjusts dynamically without recapitulating developmental fate progression.Intragenic dominant suppressors of glp-1, a gene essential for cell-signaling in Caenorhabditis elegans, support a role for cdc10/SWI6/ankyrin motifs in GLP-1 function.Structure, expression and duplication of genes which encode phosphoglyceromutase of Drosophila melanogasterThe structure and evolution of the melanocortin and MCH receptors in fish and mammals.Sequence characterization of teleost fish melanocortin receptors.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.Induction of a specific muscle cell type by a hedgehog-like protein in zebrafish.Nerve growth factor stimulates cardiac regeneration via cardiomyocyte proliferation in experimental heart failureLoss of Tropomodulin4 in the zebrafish mutant träge causes cytoplasmic rod formation and muscle weakness reminiscent of nemaline myopathy.Insights from sharks: evolutionary and developmental models of fin development.Low-cost silicone imaging casts for zebrafish embryos and larvae.Myotome meanderings. Cellular morphogenesis and the making of muscle.Evaluation of exon-skipping strategies for Duchenne muscular dystrophy utilizing dystrophin-deficient zebrafish.The zebrafish as a model for muscular dystrophy and congenital myopathy.The eIF4G-homolog p97 can activate translation independent of caspase cleavageBlockage of lysophosphatidic acid signaling improves spinal cord injury outcomes.Vertebrate myotome development.Biasing amacrine subtypes in the Atoh7 lineage through expression of Barhl2.Zebrafish models flex their muscles to shed light on muscular dystrophies.Genetic basis of hindlimb loss in a naturally occurring vertebrate model.The genetics of vertebrate myogenesis.Fgf2 improves functional recovery-decreasing gliosis and increasing radial glia and neural progenitor cells after spinal cord injury.A myogenic precursor cell that could contribute to regeneration in zebrafish and its similarity to the satellite cell.Skeletal myogenesis in the zebrafish and its implications for muscle disease modelling.
P50
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P50
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researcher
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wetenschapper
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հետազոտող
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name
Peter D. Currie
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Peter D. Currie
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Peter D. Currie
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Peter D. Currie
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Peter D. Currie
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Peter D. Currie
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Peter D. Currie
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Peter D. Currie
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Peter D. Currie
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Peter D. Currie
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Peter D. Currie
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Peter D. Currie
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Peter D. Currie
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Peter D. Currie
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Peter D. Currie
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P106
P1153
7102466249
P21
P31
P496
0000-0001-8874-8862