Lack of Apobec2-related proteins causes a dystrophic muscle phenotype in zebrafish embryos

The power of the zebrafish for disease analysis

(2009) P. W. Ingham   HUMAN MOLECULAR GENETICS

Pathological defects in congenital myopathies

(2009) Caroline A. Sewry   JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY

Developmental defects in a zebrafish model for muscular dystrophies associated with the loss of fukutin-related protein (FKRP)

(2008) Paul Thornhill et al.   BRAIN

Congenital myopathies

(2008) Adele D’Amico et al.   Current Neurology and Neuroscience Reports

Congenital myopathies

(2008) Caroline A Sewry et al.   CURRENT OPINION IN NEUROLOGY

The ATPase-dependent chaperoning activity of Hsp90a regulates thick filament formation and integration during skeletal muscle myofibrillogenesis

(2008) T. A. Hawkins et al.   DEVELOPMENT

Loss of unc45a precipitates arteriovenous shunting in the aortic arches

(2008) Matthew J. Anderson et al.   DEVELOPMENTAL BIOLOGY

Genetic isolation and characterization of a splicing mutant of zebrafish dystrophin

(2008) Jeffrey R. Guyon et al.   HUMAN MOLECULAR GENETICS

Overexpression of Myostatin2 in zebrafish reduces the expression of dystrophin associated protein complex (DAPC) which leads to muscle dystrophy

(2008) Aseervatham Anusha Amali et al.   JOURNAL OF BIOMEDICAL SCIENCE

Shuttling of the chaperones Unc45b and Hsp90a between the A band and the Z line of the myofibril

(2008) Christelle Etard et al.   JOURNAL OF CELL BIOLOGY

Zebrafish as a new animal model for movement disorders

(2008) Laura Flinn et al.   JOURNAL OF NEUROCHEMISTRY

What’s new in congenital myopathies?

(2008) Kathryn North   NEUROMUSCULAR DISORDERS