ZFIN Person: Currie, Peter D.

ZFIN ID: ZDB-PERS-970127-7

Currie, Peter D.

Email:	peter.currie@monash.edu
URL:
Affiliation:	Peter Currie Lab
Address:	Australian Regenerative Medicine Institute (ARMI) EMBL Australia Building 75, Level 1 Monash University Clayton, VIC, 3800 Australia
Country:	Australia
Phone:	61-3-99029602
Fax:	61-3-99029729
ORCID ID:

BIOGRAPHY AND RESEARCH INTERESTS

PUBLICATIONS

Tzung, K.W., Lalonde, R.L., Prummel, K.D., Mahabaleshwar, H., Moran, H.R., Stundl, J., Cass, A.N., Le, Y., Lea, R., Dorey, K., Tomecka, M.J., Zhang, C., Brombacher, E.C., White, W.T., Roehl, H.H., Tulenko, F.J., Winkler, C., Currie, P.D., Amaya, E., Davis, M.C., Bronner, M.E., Mosimann, C., Carney, T.J. (2023) A median fin derived from the lateral plate mesoderm and the origin of paired fins. Nature. 618(7965):543-549

Berger, J., Berger, S., Currie, P.D. (2022) Mob4-dependent STRIPAK involves the chaperonin TRiC to coordinate myofibril and microtubule network growth. PLoS Genetics. 18:e1010287

Berger, J., Berger, S., Mok, Y.S.G., Li, M., Tarakci, H., Currie, P.D. (2022) Genetic dissection of novel myopathy models reveals a role of CapZα and Leiomodin 3 during myofibril elongation. PLoS Genetics. 18:e1010066

Manneken, J.D., Dauer, M.V.P., Currie, P.D. (2021) Dynamics of muscle growth and regeneration: Lessons from the teleost. Experimental cell research. 411(2):112991

Wood, A.J., Lin, C.H., Li, M., Nishtala, K., Alaei, S., Rossello, F., Sonntag, C., Hersey, L., Miles, L.B., Krisp, C., Dudczig, S., Fulcher, A.J., Gibertini, S., Conroy, P.J., Siegel, A., Mora, M., Jusuf, P., Packer, N.H., Currie, P.D. (2021) FKRP-dependent glycosylation of fibronectin regulates muscle pathology in muscular dystrophy. Nature communications. 12:2951

Brandli, A., Dudczig, S., Currie, P.D., Jusuf, P.R. (2021) Photoreceptor ablation following ATP induced injury triggers Müller glia driven regeneration in zebrafish. Experimental Eye Research. 207:108569

Ratnayake, D., Nguyen, P.D., Rossello, F.J., Wimmer, V.C., Tan, J.L., Galvis, L.A., Julier, Z., Wood, A.J., Boudier, T., Isiaku, A.I., Berger, S., Oorschot, V., Sonntag, C., Rogers, K.L., Marcelle, C., Lieschke, G.J., Martino, M.M., Bakkers, J., Currie, P.D. (2021) Macrophages provide a transient muscle stem cell niche via NAMPT secretion. Nature. 591(7849):281-287

Douek, A.M., Klein, E.I., Kaslin, J., Currie, P.D., Ruparelia, A.A. (2021) Cellular and Molecular Characterization of the Effects of the Zebrafish Embryo Genotyper Protocol. Zebrafish. 18(1):92-95

Montandon, M., Currie, P.D., Ruparelia, A.A. (2021) Examining Muscle Regeneration in Zebrafish Models of Muscle Disease. Journal of visualized experiments : JoVE. (167):

Hughes, G.L., Lones, M.A., Bedder, M., Currie, P.D., Smith, S.L., Pownall, M.E. (2020) Machine learning discriminates a movement disorder in a zebrafish model of Parkinson's disease. Disease models & mechanisms. 13(10):

Berger, J., Li, M., Berger, S., Meilak, M., Rientjes, J., Currie, P.D. (2020) Effect of Ataluren on dystrophin mutations. Journal of Cellular and Molecular Medicine. 24(12):6680-6689

Hall, T.E., Wood, A.J., Ehrlich, O., Li, M., Sonntag, C.S., Cole, N.J., Huttner, I.G., Sztal, T.E., Currie, P.D. (2019) Cellular rescue in a zebrafish model of congenital muscular dystrophy type 1A. NPJ Regenerative medicine. 4:21

Keenan, S.R., Currie, P.D. (2019) The Developmental Phases of Zebrafish Myogenesis. Journal of developmental biology. 7(2)

Talbot, J.C., Teets, E.M., Ratnayake, D., Duy, P.Q., Currie, P.D., Amacher, S.L. (2019) Muscle precursor cell movements in zebrafish are dynamic and require six-family genes. Development (Cambridge, England). 146(10):

Ratnayake, D., Currie, P.D. (2019) Fluorescence-Activated Cell Sorting of Larval Zebrafish Muscle Stem/Progenitor Cells Following Skeletal Muscle Injury. Methods in molecular biology (Clifton, N.J.). 1889:245-254

Wood, A.J., Cohen, N., Joshi, V., Li, M., Costin, A., Hersey, L., McKaige, E.A., Manneken, J.D., Sonntag, C., Miles, L.B., Siegel, A., Currie, P.D. (2018) RGD inhibition of itgb1 ameliorates laminin-a2 deficient zebrafish fibre pathology. Human molecular genetics. 28(9):1403-1413

Goldshmit, Y., Tang, J.K.K.Y., Siegel, A.L., Nguyen, P.D., Kaslin, J., Currie, P.D., Jusuf, P.R. (2018) Different Fgfs have distinct roles in regulating neurogenesis after spinal cord injury in zebrafish. Neural Development. 13:24

Nguyen, P.D., Currie, P.D. (2018) Guidelines and best practices in successfully using Zebrabow for lineage tracing multiple cells within tissues. Methods (San Diego, Calif.). 150:63-67

Dauer, M.V.P., Currie, P.D., Berger, J. (2018) Skeletal malformations of Meox1-deficient zebrafish resemble human Klippel-Feil syndrome. Journal of anatomy. 233(6):687-695

Jung, H., Baek, M., D'Elia, K.P., Boisvert, C., Currie, P.D., Tay, B.H., Venkatesh, B., Brown, S.M., Heguy, A., Schoppik, D., Dasen, J.S. (2018) The Ancient Origins of Neural Substrates for Land Walking. Cell. 172:667-682.e15

Thomasi, A.B.D., Sonntag, C., Pires, D.F., Zuidema, D., Benci, A., Currie, P.D., Wood, A.J. (2018) A Low-Cost Pulse Generator for Exacerbating Muscle Fiber Detachment Phenotypes in Zebrafish. Zebrafish. 15(4):420-424

Berger, J., Berger, S., Li, M., Jacoby, A.S., Arner, A., Bavi, N., Stewart, A.G., Currie, P.D. (2018) In Vivo Function of the Chaperonin TRiC in α-Actin Folding during Sarcomere Assembly. Cell Reports. 22:313-322

Masselink, W., Masaki, M., Sieiro, D., Marcelle, C., Currie, P.D. (2017) Phosphorylation of Lbx1 controls lateral myoblast migration into the limb. Developmental Biology. 430:302-309

Dudczig, S., Currie, P.D., Jusuf, P.R. (2017) Developmental and adult characterization of secretagogin expressing amacrine cells in zebrafish retina. PLoS One. 12:e0185107

Ng Chi Kei, J., Currie, P.D., Jusuf, P.R. (2017) Fate bias during neural regeneration adjusts dynamically without recapitulating developmental fate progression. Neural Development. 12:12

Nguyen, P.D., Gurevich, D.B., Sonntag, C., Hersey, L., Alaei, S., Nim, H.T., Siegel, A., Hall, T.E., Rossello, F.J., Boyd, S.E., Polo, J.M., Currie, P.D. (2017) Muscle Stem Cells Undergo Extensive Clonal Drift during Tissue Growth via Meox1-Mediated Induction of G2 Cell-Cycle Arrest. Cell Stem Cell. 21:107-119.e6

Goodings, L., He, J., Wood, A., Harris, W.A., Currie, P.D., Jusuf, P.R. (2017) In vivo expression of Nurr1/Nr4a2a in developing retinal amacrine subtypes in zebrafish Tg(nr4a2a:eGFP) transgenics. The Journal of comparative neurology. 525(8):1962-1979

Dudczig, S., Currie, P.D., Poggi, L., Jusuf, P.R. (2017) In Vivo Imaging of Transgenic Gene Expression in Individual Retinal Progenitors in Chimeric Zebrafish Embryos to Study Cell Nonautonomous Influences. Journal of visualized experiments : JoVE. (121)

Berger, J., Berger, S., Li, M., Currie, P.D. (2017) Myo18b is essential for sarcomere assembly in fast skeletal muscle. Human molecular genetics. 26(6):1146-1156

Nguyen, P.D., Currie, P.D. (2017) Using Transgenic Zebrafish to Study Muscle Stem/Progenitor Cells. Methods in molecular biology (Clifton, N.J.). 1556:117-125

Sztal, T.E., Currie, P.D., Bryson-Richardson, R.J. (2017) Analysis of RNA Expression in Adult Zebrafish Skeletal Muscle. Methods in molecular biology (Clifton, N.J.). 1668:27-35

Li, M., Hromowyk, K.J., Amacher, S.L., Currie, P.D. (2017) Muscular dystrophy modeling in zebrafish. Methods in cell biology. 138:347-380

Ng Chi Kei, J., Dudczig, S., Currie, P.D., Jusuf, P.R. (2016) Feedback from each retinal neuron population drives expression of subsequent fate determinant genes without influencing the cell cycle exit timing. The Journal of comparative neurology. 524(13):2553-66

Masselink, W., Cole, N.J., Fenyes, F., Berger, S., Sonntag, C., Wood, A., Nguyen, P.D., Cohen, N., Knopf, F., Weidinger, G., Hall, T.E., Currie, P.D. (2016) A somitic contribution to the apical ectodermal ridge is essential for fin formation. Nature. 535(7613):542-6

Gurevich, D.B., Nguyen, P.D., Siegel, A.L., Ehrlich, O.V., Sonntag, C., Phan, J.M., Berger, S., Ratnayake, D., Hersey, L., Berger, J., Verkade, H., Hall, T.E., Currie, P.D. (2016) Asymmetric division of clonal muscle stem cells coordinates muscle regeneration in vivo. Science (New York, N.Y.). 353(6295):aad9969

Don, E.K., de Jong-Curtain, T.A., Doggett, K., Hall, T.E., Heng, B., Badrock, A.P., Winnick, C., Nicholson, G.A., Guillemin, G.J., Currie, P.D., Hesselson, D., Heath, J.K., Cole, N.J. (2016) Genetic basis of hindlimb loss in a naturally occurring vertebrate model. Biology Open. 5(3):359-66

Sztal, T.E., Zhao, M., Williams, C., Oorschot, V., Parslow, A.C., Giousoh, A., Yuen, M., Hall, T.E., Costin, A., Ramm, G., Bird, P.I., Busch-Nentwich, E.M., Stemple, D.L., Currie, P.D., Cooper, S.T., Laing, N.G., Nowak, K.J., Bryson-Richardson, R.J. (2015) Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function. Acta Neuropathologica. 130(3):389-406

Goldshmit, Y., Frisca, F., Kaslin, J., Pinto, A.R., Tang, J.K., Pébay, A., Pinkas-Kramarski, R., Currie, P.D. (2015) Decreased anti-regenerative effects after spinal cord injury in spry4-/- mice. Neuroscience. 287:104-12

Berger, J., Hall, T.E., Currie, P.D. (2015) Novel Transgenic Lines to Label Sarcolemma and Myofibrils of the Musculature. Zebrafish. 12(1):124-5

Gurevich, D., Siegel, A., Currie, P.D. (2015) Skeletal Myogenesis in the Zebrafish and Its Implications for Muscle Disease Modelling. Results and problems in cell differentiation. 56:49-76

Berger, J., Tarakci, H., Berger, S., Li, M., Hall, T.E., Arner, A., Currie, P.D. (2014) Loss of tropomodulin4 in the zebrafish mutant träge causes cytoplasmic rod formation and muscle weakness reminiscent of nemaline myopathy. Disease models & mechanisms. 7(12):1407-15

Wood, A.J., Currie, P.D. (2014) Analysing regenerative potential in zebrafish models of congenital muscular dystrophy. The international journal of biochemistry & cell biology. 56C:30-37

Nguyen, P.D., Hollway, G.E., Sonntag, C., Miles, L.B., Hall, T.E., Berger, S., Fernandez, K.J., Gurevich, D.B., Cole, N.J., Alaei, S., Ramialison, M., Sutherland, R.L., Polo, J.M., Lieschke, G.J., Currie, P.D. (2014) Haematopoietic stem cell induction by somite-derived endothelial cells controlled by meox1. Nature. 512(7514):314-8

Ng, J., Currie, P., Jusuf, P. R. (2014) The Regenerative Potential of the Vertebrate Retina: Lessons from the Zebrafish. Regenerative Biology of the Eye. :49-82

Masselink, W., Wong, J.C., Liu, B., Fu, J., and Currie, P.D. (2014) Low-Cost Silicone Imaging Casts for Zebrafish Embryos and Larvae. Zebrafish. 11(1):26-31

Giacomotto, J., Brouilly, N., Walter, L., Mariol, M.C., Berger, J., Ségalat, L., Becker, T.S., Currie, P.D., and Gieseler, K. (2013) Chemical genetics unveils a key role of mitochondrial dynamics, cytochrome c release and IP3R activity in muscular dystrophy. Human molecular genetics. 22(22):4562-78

Siegel, A.L., Gurevich, D.B., and Currie, P.D. (2013) A myogenic precursor cell that could contribute to regeneration in zebrafish and its similarity to the satellite cell. The FEBS journal. 280(17):4074-88

Berger, J., and Currie, P.D. (2013) 503unc, a small and muscle-specific zebrafish promoter. Genesis (New York, N.Y. : 2000). 51(6):443-7

Don, E.K., Currie, P.D., Cole, N.J. (2013) The evolutionary history of the development of the pelvic fin/hindlimb. Journal of anatomy. 222:114-133

Sztal, T.E., Sonntag, C., Hall, T.E., and Currie, P.D. (2012) Epistatic dissection of laminin-receptor interactions in dystrophic zebrafish muscle. Human molecular genetics. 21(21):4718-4731

Berger, J., and Currie, P.D. (2012) Zebrafish models flex their muscles to shed light on muscular dystrophies. Disease models & mechanisms. 5(6):726-732

Jusuf, P.R., Albadri, S., Paolini, A., Currie, P.D., Argenton, F., Higashijima, S., Harris, W.A., and Poggi, L. (2012) Biasing Amacrine Subtypes in the Atoh7 Lineage through Expression of Barhl2. The Journal of neuroscience : the official journal of the Society for Neuroscience. 32(40):13929-13944

Ruparelia, A.A., Zhao, M., Currie, P.D., and Bryson-Richardson, R.J. (2012) Characterization and Investigation of zebrafish models of Filamin related myofibrillar myopathy. Human molecular genetics. 21(18):4073-4083

Goldshmit, Y., Matteo, R., Sztal, T., Ellett, F., Frisca, F., Moreno, K., Crombie, D., Lieschke, G.J., Currie, P.D., Sabbadini, R.A., and Pebay, A. (2012) Blockage of Lysophosphatidic Acid Signaling Improves Spinal Cord Injury Outcomes. The American journal of pathology. 181(3):978-992

Johnson, J.L., Hall, T.E., Dyson, J.M., Sonntag, C., Ayers, K., Berger, S., Gautier, P., Mitchell, C., Hollway, G.E., and Currie, P.D. (2012) Scube activity is necessary for Hedgehog signal transduction in vivo. Developmental Biology. 368(2):193-202

Berger, J., Sztal, T., and Currie, P.D. (2012) Quantification of birefringence readily measures the level of muscle damage in zebrafish. Biochemical and Biophysical Research Communications. 423(4):785-788

Goldshmit, Y., Sztal, T.E., Jusuf, P.R., Hall, T.E., Nguyen-Chi, M., and Currie, P.D. (2012) Fgf-dependent glial cell bridges facilitate spinal cord regeneration in zebrafish. The Journal of neuroscience : the official journal of the Society for Neuroscience. 32(22):7477-7492

Cole, N.J., Currie, P. (2012) Shaping muscle bioarchitecture for the fin to limb transition.. Bioarchitecture. 2(3):98-103

Gupta, V.A., Kawahara, G., Myers, J.A., Chen, A.T., Hall, T.E., Manzini, M.C., Currie, P.D., Zhou, Y., Zon, L.I., Kunkel, L.M., and Beggs, A.H. (2012) A Splice Site Mutation in Laminin-alpha2 Results in a Severe Muscular Dystrophy and Growth Abnormalities in Zebrafish. PLoS One. 7(8):e43794

Lam, N.T., Currie, P.D., Lieschke, G.J., Rosenthal, N.A., and Kaye, D.M. (2012) Nerve Growth Factor Stimulates Cardiac Regeneration via Cardiomyocyte Proliferation in Experimental Heart Failure. PLoS One. 7(12):e53210

Nguyen-Chi, M.E., Bryson-Richardson, R., Sonntag, C., Hall, T.E., Gibson, A., Sztal, T., Chua, W., Schilling, T.F., and Currie, P.D. (2012) Morphogenesis and Cell Fate Determination within the Adaxial Cell Equivalence Group of the Zebrafish Myotome. PLoS Genetics. 8(10):e1003014

Berger, J., Berger, S., Jacoby, A.S., Wilton, S.D., and Currie, P.D. (2011) Evaluation of Exon-Skipping Strategies for Duchenne Muscular Dystrophy Utilizing Dystrophin-deficient Zebrafish. Journal of Cellular and Molecular Medicine. 15(12):2643-51

Cole, N.J., Hall, T.E., Don, E.K., Berger, S., Boisvert, C.A., Neyt, C., Ericsson, R., Joss, J., Gurevich, D.B., and Currie, P.D. (2011) Development and evolution of the muscles of the pelvic fin. PLoS Biology. 9(10):e1001168

Williams, R.J., Hall, T.E., Glattauer, V., White, J., Pasic, P.J., Sorensen, A.B., Waddington, L., McLean, K.M., Currie, P.D., and Hartley, P.G. (2011) The in vivo performance of an enzyme-assisted self-assembled peptide/protein hydrogel. Biomaterials. 32(22):5304-5310

Don, E.K., Hall, T.E., Currie, P.D., and Cole, N.J. (2011) Morphology of pelvic fin loss in a zebrafish strain (Danio rerio). Journal of morphology. 272(5):583-589

Sztal, T., Berger, S., Currie, P.D., and Hall, T.E. (2011) Characterization of the laminin gene family and evolution in zebrafish. Developmental Dynamics : an official publication of the American Association of Anatomists. 240(2):422-431

Tao, S., Witte, M., Bryson-Richardson, R.J., Currie, P.D., Hogan, B.M., and Schulte-Merker, S. (2011) Zebrafish prox1b Mutants Develop a Lymphatic Vasculature, and prox1b Does Not Specifically Mark Lymphatic Endothelial Cells. PLoS One. 6(12):e28934

Berger, J., Berger, S., Hall, T.E., Lieschke, G.J., and Currie, P.D. (2010) Dystrophin-deficient zebrafish feature aspects of the Duchenne muscular dystrophy pathology. Neuromuscular disorders : NMD. 20(12):826-832

Jacoby, A.S., Busch-Nentwich, E., Bryson-Richardson, R.J., Hall, T.E., Berger, J., Berger, S., Sonntag, C., Sachs, C., Geisler, R., Stemple, D.L., and Currie, P.D. (2009) The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachment. Development (Cambridge, England). 136(19):3367-3376

Currie, P.D., Schilling, T.F., and Ingham, P.W. (2008) Small-scale marker-based screening for mutations in zebrafish development (2008). Methods in molecular biology (Clifton, N.J.). 461:493-512

Daggett, D.F., Domingo, C.R., Currie, P.D., and Amacher, S.L. (2007) Control of morphogenetic cell movements in the early zebrafish myotome. Developmental Biology. 309(2):169-179

Cole, N.J., Currie, P.D. (2007) Insights from sharks: evolutionary and developmental models of fin development.. Developmental Dynamics : an official publication of the American Association of Anatomists. 236(9):2421-31

Bryson-Richardson, R.J., Berger, S., Schilling, T.F., Hall, T.E., Cole, N.J., Gibson, A.J., Sharpe, J., and Currie, P.D. (2007) FishNet: an online database of zebrafish anatomy. BMC Biology. 5(1):34

Lieschke, G.J., and Currie, P.D. (2007) Animal models of human disease: zebrafish swim into view. Nature reviews. Genetics. 8(5):353-367

Hall, T.E., Bryson-Richardson, R.J., Berger, S., Jacoby, A.S., Cole, N.J., Hollway, G.E., Berger, J., and Currie, P.D. (2007) The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin {alpha}2-deficient congenital muscular dystrophy. Proceedings of the National Academy of Sciences of the United States of America. 104(17):7092-7097

Nousch, M., Reed, V., Bryson-Richardson, R.J., Currie, P.D., and Preiss, T. (2007) The eIF4G-homolog p97 can activate translation independent of caspase cleavage. RNA (New York, N.Y.). 13(3):374-384

Svetic, V., Hollway, G.E., Elworthy, S., Chipperfield, T.R., Davison, C., Adams, R.J., Eisen, J.S., Ingham, P.W., Currie, P.D., and Kelsh, R.N. (2007) Sdf1a patterns zebrafish melanophores and links the somite and melanophore pattern defects in choker mutants. Development (Cambridge, England). 134(5):1011-1022

Hollway, G.E., Bryson-Richardson, R.J., Berger, S., Cole, N.J., Hall, T.E., and Currie, P.D. (2007) Whole-somite rotation generates muscle progenitor cell compartments in the developing zebrafish embryo. Developmental Cell. 12(2):207-219

Berger, J., and Currie, P. (2007) The role of zebrafish in chemical genetics. Current Medicinal Chemistry. 14(22):2413-2420

Hollway, G.E., Maule, J., Gautier, P., Evans, T.M., Keenan, D.G., Lohs, C., Fischer, D., Wicking, C., and Currie, P.D. (2006) Scube2 mediates Hedgehog signalling in the zebrafish embryo. Developmental Biology. 294(1):104-118

Hall, T.E., Bryson-Richardson, R.J., Cole, N.J., Currie, P.D. (2005) Muscle stem cells and regeneration in zebrafish models of muscular dystrophies. Mechanisms of Development. 122:S131

Cole, N.J., Neyt, C., Currie, P.D. (2005) Morphogenesis and evolution of vertebrate appendicular muscle formation. Mechanisms of Development. 122:S160

Nixon, S.J., Wegner, J., Ferguson, C., Méry, P.F., Hancock, J.F., Currie, P.D., Key, B., Westerfield, M., and Parton, R.G. (2005) Zebrafish as a model for caveolin-associated muscle disease; caveolin-3 is required for myofibril organization and muscle cell patterning. Human molecular genetics. 14(13):1727-1743

Bryson-Richardson, R.J., Daggett, D.F., Cortes, F., Neyt, C., Keenan, D.G., and Currie, P.D. (2005) Myosin heavy chain expression in zebrafish and slow muscle composition. Developmental Dynamics : an official publication of the American Association of Anatomists. 233(3):1018-1022

Haines, L., Neyt, C., Gautier, P., Keenan, D.G., Bryson-Richardson, R.J., Hollway, G.E., Cole, N.J., Currie, P.D. (2004) Met and Hgf signaling controls hypaxial muscle and lateral line development in the zebrafish. Development (Cambridge, England). 131(19):4857-4869

Daggett, D.F., Boyd, C.A,. Gautier, P., Bryson-Richardson, R.J., Thisse, C., Thisse, B., Amacher, S.L., and Currie, P.D. (2004) Developmentally restricted actin-regulatory molecules control morphogenetic cell movements in the zebrafish gastrula. Current biology : CB. 14(18):632-638

Bassett, D., and Currie, P.D. (2004) Identification of a zebrafish model of muscular dystrophy. Clinical and experimental pharmacology & physiology. 31(8):537-540

Bryson-Richardson, RJ., and Currie, P.D. (2004) Optical projection tomography for spatio-temporal analysis in the zebrafish. The Zebrafish: Cellular and Developmental Biology,2nd Ed. Methods Cell Biol.. 76:37-50

Cortés, F., Daggett, D., Bryson-Richardson, R.J., Neyt, C., Maule, J., Gautier, P., Hollway, G.E., Keenan, D., and Currie, P.D. (2003) Cadherin-mediated differential cell adhesion controls slow muscle cell migration in the developing zebrafish myotome. Developmental Cell. 5(6):865-876

Bassett, D.I., Bryson-Richardson, R.J., Daggett, D.F., Gautier, P., Kennan, D.G., and Currie, P.D. (2003) Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo. Development (Cambridge, England). 130(23):5851-5860

Bassett, D.I. and Currie, P.D. (2003) The zebrafish as a model for muscular dystrophy and congenital myopathy. Human molecular genetics. (Suppl. 2) 12:R265-R270

Logan, D.W., Bryson-Richardson, R.J., Taylor, M.S., Currie, P., and Jackson, I.J. (2003) Sequence characterization of teleost fish melanocortin receptors. Annals of the New York Academy of Sciences. 994:319-330

Logan, D.W., Bryson-Richardson, R.J., Pagan, K.E., Taylor, M.S., Currie, P.D., and Jackson, I.J. (2003) The structure and evolution of the melanocortin and MCH receptors in fish and mammals. Genomics. 81(2):184-191

Hammond, K.L., Hill, R.E., Whitfield, T.T., and Currie, P.D. (2002) Isolation of three zebrafish dachshund homologues and their expression in sensory organs, the central nervous system and pectoral fin buds. Mechanisms of Development. 112(1-2):183-189

Nikolic, V., Hollway, G., Adams, R.J., Kelsh, R.N., and Currie, P. (2002) Characterization of a zebrafish pigment pattern mutant, choker. Pigm. Cell Res.. 15(9):27-28

Brennan, C., Amacher, S.L., and Currie, P.D. (2002) Somitogenesis. Results and problems in cell differentiation. 40:271-297

Haines, L. and Currie, P.D. (2001) Morphogenesis and evolution of vertebrate appendicular muscle. Journal of anatomy. 199(1-2):205-209

Neyt, C., Jagla, K., Thisse, C., Thisse, B., Haines, L., and Currie, P.D. (2000) Evolutionary origins of vertebrate appendicular muscle. Nature. 408(6808):82-86

Norris, W., Neyt, C., Ingham, P.W., and Currie, P.D. (2000) Slow muscle induction by Hedgehog signalling in vitro. Journal of Cell Science. 113(Pt.15):2695-2703

Hollway, G.E. and Currie, P.D. (2000) Zebrafish earn their stripes. Trends in genetics : TIG. 16(5):236

Lewis, K.E., Currie, P.D., Roy, S., Schauerte, H., Haffter, P., and Ingham, P.W. (1999) Control of muscle cell-type specification in the zebrafish embryo by hedgehog signalling. Developmental Biology. 216(2):469-480

Currie, P.D., Schilling, T.F., and Ingham, P.W. (1999) Small-scale marker-based screening for mutations in zebrafish development. Methods in molecular biology (Clifton, N.J.). 97:441-460

Currie P.D. (1998) Hedgehogs escape from Pandora's box. Journal of molecular medicine (Berlin, Germany). 76:421-433

Currie P.D. and Ingham P.W. (1998) The generation and interpretation of positional information within the vertebrate myotome. Mechanisms of Development. 73:3-21

Blagden, C.S., P.D. Currie, P.W. Ingham, and S.M. Hughes (1997) Notochord induction of zebrafish slow muscle mediated by Sonic hedgehog. Genes & Development. 11(17):2163-2175

Currie, P.D. (1996) Zebrafish genetics: Mutant cornucopia. Current biology : CB. 6(12):1548-1552

Currie, P.D. and Ingham, P.W. (1996) Induction of a specific muscle cell type by a hedgehog-like protein in zebrafish. Nature. 382(6590):452-455

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