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2015 Journal Article The caveolin-cavin system plays a conserved and critical role in mechanoprotection of skeletal muscleLo, Harriet P., Nixon, Susan J., Hall, Thomas E., Cowling, Belinda S., Ferguson, Charles, Morgan, Garry P., Schieber, Nicole L., Fernandez-Rojo, Manuel A., Bastiani, Michele, Floetenmeyer, Matthias, Martel, Nick, Laporte, Jocelyn, Pilch, Paul F. and Parton, Robert G. (2015). The caveolin-cavin system plays a conserved and critical role in mechanoprotection of skeletal muscle. Journal of Cell Biology, 210 (5), 833-849. doi: 10.1083/jcb.201501046 |
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2015 Journal Article In vivo characterization of microglial engulfment of dying neurons in the zebrafish spinal cordMorsch, Marco, Radford, Rowan, Lee, Albert, Don, Emily K., Bedrock, Andrew P., Hall, Thomas E., Cole, Nicholas J. and Chung, Roger (2015). In vivo characterization of microglial engulfment of dying neurons in the zebrafish spinal cord. Frontiers in Cellular Neuroscience, 9 (August) 321, 321-321. doi: 10.3389/fncel.2015.00321 |
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2015 Journal Article Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle functionSztal, Tamar E., Zhao, Mo, Williams, Caitlin, Oorschot, Viola, Parslow, Adam C., Giousoh, Aminah, Yuen, Michaela, Hall, Thomas E., Costin, Adam, Ramm, Georg, Bird, Phillip I., Busch-Nentwich, Elisabeth M., Stemple, Derek L., Currie, Peter D., Cooper, Sandra T., Laing, Nigel G., Nowak, Kristen J. and Bryson-Richardson, Robert J. (2015). Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function. Acta Neuropathologica, 130 (3), 389-406. doi: 10.1007/s00401-015-1430-3 |
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2015 Journal Article Novel transgenic lines to label sarcolemma and myofibrils of the musculatureBerger, Joachim, Hall, Thomas E. and Currie, Peter D. (2015). Novel transgenic lines to label sarcolemma and myofibrils of the musculature. Zebrafish, 12 (1), 124-125. doi: 10.1089/zeb.2014.1065 |
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2014 Journal Article Loss of tropomodulin4 in the zebrafish mutant träge causes cytoplasmic rod formation and muscle weakness reminiscent of nemaline myopathyBerger, Joachim, Tarakci, Hakan, Berger, Silke, Li, Mei, Hall, Thomas E., Arner, Anders and Currie, Peter D. (2014). Loss of tropomodulin4 in the zebrafish mutant träge causes cytoplasmic rod formation and muscle weakness reminiscent of nemaline myopathy. DMM Disease Models and Mechanisms, 7 (12), 1407-1415. doi: 10.1242/dmm.017376 |
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2014 Journal Article Haematopoietic stem cell induction by somite-derived endothelial cells controlled by meox1Nguyen, Phong Dang, Hollway, Georgina Elizabeth, Sonntag, Carmen, Miles, Lee Barry, Hall, Thomas Edward, Berger, Silke, Fernandez, Kristine Joy, Gurevich, David Baruch, Cole, Nicholas James, Alaei, Sara, Ramialison, Mirana, Sutherland, Robert Lyndsay, Polo, Jose Maria, Lieschke, Graham John and Currie, Peter David (2014). Haematopoietic stem cell induction by somite-derived endothelial cells controlled by meox1. Nature, 512 (7514), 314-318. doi: 10.1038/nature13678 |
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2014 Journal Article Mutant human FUS is ubiquitously mislocalized and generates persistent stress granules in primary cultured transgenic zebrafish cellsAcosta, Jamie Rae, Goldsbury, Claire, Winnick, Claire, Badrock, Andrew P., Fraser, Stuart T., Laird, Angela S., Hall, Thomas E., Don, Emily K., Fifita, Jennifer A., Blair, Ian P., Nicholson, Garth A. and Cole, Nicholas J. (2014). Mutant human FUS is ubiquitously mislocalized and generates persistent stress granules in primary cultured transgenic zebrafish cells. PLoS One, 9 (6) e90572, e90572.1-e90572.9. doi: 10.1371/journal.pone.0090572 |
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2012 Journal Article Epistatic dissection of laminin–receptor interactions in dystrophic zebrafish muscleSztal, Tamar E., Sonntag, Carmen, Hall, Thomas E. and Currie, Peter D. (2012). Epistatic dissection of laminin–receptor interactions in dystrophic zebrafish muscle. Human Molecular Genetics, 21 (21) dds312, 4718-4731. doi: 10.1093/hmg/dds312 |
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2012 Journal Article A splice site mutation in Laminin-α2 results in a severe muscular dystrophy and growth abnormalities in ZebrafishGupta, Vandana A., Kawahara, Genri, Myers, Jennifer A., Chen, Aye T., Hall, Thomas E., Manzini, M. Chiara, Currie, Peter D., Zhou, Yi, Zon, Leonard I., Kunkel, Louis M. and Beggs, Alan H. (2012). A splice site mutation in Laminin-α2 results in a severe muscular dystrophy and growth abnormalities in Zebrafish. PLoS One, 7 (8) e43794, e43794.1-e43794.9. doi: 10.1371/journal.pone.0043794 |
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2012 Journal Article Scube activity is necessary for Hedgehog signal transduction in vivoJohnson, Jacque-Lynne F. A., Hall, Thomas E., Dyson, Jennifer M., Sonntag, Carmen, Ayers, Katie, Berger, Silke, Gautier, Philippe, Mitchell, Christina, Hollway, Georgina E. and Currie, Peter D. (2012). Scube activity is necessary for Hedgehog signal transduction in vivo. Developmental Biology, 368 (2), 193-202. doi: 10.1016/j.ydbio.2012.05.007 |
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2012 Journal Article Fgf-dependent glial cell bridges facilitate spinal cord regeneration in ZebrafishGoldshmit, Yona, Sztal, Tamar E., Jusuf, Patricia R., Hall, Thomas E., Nguyen-Chi, Mai and Currie, Peter D. (2012). Fgf-dependent glial cell bridges facilitate spinal cord regeneration in Zebrafish. Journal of Neuroscience, 32 (22), 7477-7492. doi: 10.1523/JNEUROSCI.0758-12.2012 |
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2012 Journal Article Morphogenesis and Cell Fate Determination within the Adaxial Cell Equivalence Group of the Zebrafish MyotomeNguyen-Chi, Mai E., Bryson-Richardson, Robert, Sonntag, Carmen, Hall, Thomas E., Gibson, Abigail, Szta,l Tamar, Chua, Wendy, Schilling, Thomas F. and Currie, Peter D. (2012). Morphogenesis and Cell Fate Determination within the Adaxial Cell Equivalence Group of the Zebrafish Myotome. PLoS Genetics, 8 (10) e1003014, e1003014.1-e1003014.16. doi: 10.1371/journal.pgen.1003014 |
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2011 Journal Article Development and evolution of the muscles of the pelvic finCole, Nicholas J., Hall, Thomas E., Don, Emily K., Berger, Silke, Boisvert, Catherine A., Neyt, Christine, Ericsson, Rolf, Joss, Jean, Gurevich, David B. and Currie, Peter D. (2011). Development and evolution of the muscles of the pelvic fin. PLoS Biology, 9 (10) e1001168, 1-10. doi: 10.1371/journal.pbio.1001168 |
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2011 Journal Article The in vivo performance of an enzyme-assisted self-assembled peptide/protein hydrogelWilliams, Richard J., Hall, Thomas E., Glattauer, Veronica, White, Jacinta, Pasic, Paul J., Sorensen, Anders B., Waddington, Lynne, McLean, Keith M., Currie, Peter D. and Hartley, Patrick G. (2011). The in vivo performance of an enzyme-assisted self-assembled peptide/protein hydrogel. Biomaterials, 32 (22), 5304-5310. doi: 10.1016/j.biomaterials.2011.03.078 |
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2011 Journal Article Morphology of pelvic fin loss in a zebrafish strain (Danio rerio)Don, Emily K., Hall, Thomas E., Currie, Peter D. and Cole, Nicholas J. (2011). Morphology of pelvic fin loss in a zebrafish strain (Danio rerio). Journal of Morphology, 272 (5), 583-589. doi: 10.1002/jmor.10938 |
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2011 Journal Article Characterization of the laminin gene family and evolution in zebrafishSztal, Tamar, Berger, Silke, Currie, Peter D. and Hall, Thomas E. (2011). Characterization of the laminin gene family and evolution in zebrafish. Developmental Dynamics, 240 (2), 422-431. doi: 10.1002/dvdy.22537 |
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2010 Journal Article Dystrophin-deficient zebrafish feature aspects of the Duchenne muscular dystrophy pathologyBerger, Joachim, Berger, Silke, Hall, Thomas E., Lieschke, Graham J. and Currie, Peter D. (2010). Dystrophin-deficient zebrafish feature aspects of the Duchenne muscular dystrophy pathology. Neuromuscular Disorders, 20 (12), 826-832. doi: 10.1016/j.nmd.2010.08.004 |
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2009 Journal Article The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachmentJacoby, Arie S., Busch-Nentwich, Elisabeth, Bryson-Richardson, Robert J., Hall, Thomas E., Berger, Joachim, Berger, Silke, Sonntag, Carmen, Sachs, Caroline, Geisler, Robert, Stemple, Derek L. and Currie, Peter D. (2009). The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachment. Development, 136 (19), 3367-3376. doi: 10.1242/dev.034561 |
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2007 Journal Article FishNet: An online database of zebrafish anatomyBryson-Richardson, Robert J., Berger, Silke, Schilling, Thomas F., Hall, Thomas E., Cole, Nicholas J., Gibson, Abigail J., Sharpe, James and Currie, Peter D. (2007). FishNet: An online database of zebrafish anatomy. BMC Biology, 5 (1) 34, 34.1-34.8. doi: 10.1186/1741-7007-5-34 |
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2007 Journal Article The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin α2-deficient congential muscular dystrophyHall, Thomas E., Bryson-Richardson, Robert J., Berger, Silke, Jacoby, Arie S., Cole, Nicholas J., Hollway, Georgina E., Berger, Joachim and Currie, Peter D. (2007). The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin α2-deficient congential muscular dystrophy. Proceedings of the National Academy of Sciences, 104 (17), 7092-7097. doi: 10.1073/pnas.0700942104 |
