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Departments of Pediatrics and Neurology
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Mammalian germ-line transgenesis by transposition.
Proceedings of the National Academy of Sciences of the United States of America Apr, 2002 | Pubmed ID: 11904379
Efficient gene delivery and gene expression in zebrafish using the Sleeping Beauty transposon.
Developmental biology Nov, 2003 | Pubmed ID: 14597195
Enhancer trapping in zebrafish using the Sleeping Beauty transposon.
BMC genomics Sep, 2004 | Pubmed ID: 15347431
Sleeping Beauty transposon for efficient gene delivery.
Methods in cell biology , 2004 | Pubmed ID: 15602921
Gene-breaking transposon mutagenesis reveals an essential role for histone H2afza in zebrafish larval development.
Mechanisms of development Jul, 2006 | Pubmed ID: 16859902
Use of the Sleeping Beauty transposon system for stable gene expression in mouse embryonic stem cells.
Cold Spring Harbor protocols Aug, 2009 | Pubmed ID: 20147246
Dominant mutation of CCDC78 in a unique congenital myopathy with prominent internal nuclei and atypical cores.
American journal of human genetics Aug, 2012 | Pubmed ID: 22818856
Novel deletion of lysine 7 expands the clinical, histopathological and genetic spectrum of TPM2-related myopathies.
Brain : a journal of neurology Feb, 2013 | Pubmed ID: 23413262
Two dynamin-2 genes are required for normal zebrafish development.
PloS one , 2013 | Pubmed ID: 23418470
Defective tubulation associated with the myopathy causing S619L DNM2 mutation.
Disease models & mechanisms Oct, 2013 | Pubmed ID: 24135484
Fluoxetine prevents dystrophic changes in a zebrafish model of Duchenne muscular dystrophy.
Human molecular genetics Sep, 2014 | Pubmed ID: 24760771
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy.
The Journal of clinical investigation Nov, 2014 | Pubmed ID: 25250574
The Journal of clinical investigation Jan, 2015 | Pubmed ID: 25654555
University of Michigan
The Hospital for Sick Children
The University of Toronto
Eric J. Horstick1,
Elizabeth M. Gibbs1,
Xingli Li1,
Ann E. Davidson1,
James J. Dowling1
1Departments of Pediatrics and Neurology, University of Michigan
Sarah J. Smith*,1,2,
Eric J. Horstick*,3,4,
Ann E. Davidson1,2,
James Dowling1,2,4
1Program in Genetics & Genome Biology, The Hospital for Sick Children,
2Department of Molecular Genetics, The University of Toronto,
3Program in Genomics of Differentiation, Eunice Kennedy Shriver National Institute of Child Health and Human Development,
4Departments of Pediatrics and Neurology, University of Michigan
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