Ann E. Davidson

Mammalian germ-line transgenesis by transposition.

Efficient gene delivery and gene expression in zebrafish using the Sleeping Beauty transposon.

Enhancer trapping in zebrafish using the Sleeping Beauty transposon.

Sleeping Beauty transposon for efficient gene delivery.

Gene-breaking transposon mutagenesis reveals an essential role for histone H2afza in zebrafish larval development.

Use of the Sleeping Beauty transposon system for stable gene expression in mouse embryonic stem cells.

Dominant mutation of CCDC78 in a unique congenital myopathy with prominent internal nuclei and atypical cores.

Novel deletion of lysine 7 expands the clinical, histopathological and genetic spectrum of TPM2-related myopathies.

Two dynamin-2 genes are required for normal zebrafish development.

Defective tubulation associated with the myopathy causing S619L DNM2 mutation.

Fluoxetine prevents dystrophic changes in a zebrafish model of Duchenne muscular dystrophy.

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

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