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Ann E. Davidson

Departments of Pediatrics and Neurology

University of Michigan

BIOGRAPHY

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PUBLICATIONS

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

Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy.

The Journal of clinical investigation Jan, 2015 | Pubmed ID: 25654555

INSTITUTIONS

University of Michigan

The Hospital for Sick Children

The University of Toronto

JOVE ARTICLES

Analysis of Embryonic and Larval Zebrafish Skeletal Myofibers from Dissociated Preparations

Eric J. Horstick¹,

Elizabeth M. Gibbs¹,

Xingli Li¹,

Ann E. Davidson¹,

James J. Dowling¹

¹Departments of Pediatrics and Neurology, University of Michigan

Biology

Analysis of Zebrafish Larvae Skeletal Muscle Integrity with Evans Blue Dye

Sarah J. Smith^*,1,2,

Eric J. Horstick^*,3,4,

Ann E. Davidson^1,2,

James Dowling^1,2,4

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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Ann E. Davidson

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Departments of Pediatrics and Neurology

University of Michigan

Analysis of Embryonic and Larval Zebrafish Skeletal Myofibers from Dissociated Preparations

Analysis of Zebrafish Larvae Skeletal Muscle Integrity with Evans Blue Dye

Departments of Pediatrics and Neurology