Elizabeth M. Gibbs

Membrane traffic and muscle: lessons from human disease.

Loss of myotubularin function results in T-tubule disorganization in zebrafish and human myotubular myopathy.

The role of MTMR14 in autophagy and in muscle disease.

Synapses on demand require dendrites at the ready: how defining stages of dendritic development in vitro could inform studies of behaviorally driven information storage in the brain.

Congenital myopathies: an update.

Neuromuscular junction abnormalities in DNM2-related centronuclear myopathy.

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

Hemimegalencephaly, a paradigm for somatic postzygotic neurodevelopmental disorders.

Swimming into prominence: the zebrafish as a valuable tool for studying human myopathies and muscular dystrophies.

Defective tubulation associated with the myopathy causing S619L DNM2 mutation.

Differentiation-related glycan epitopes identify discrete domains of the muscle glycocalyx.

High levels of sarcospan are well tolerated and act as a sarcolemmal stabilizer to address skeletal muscle and pulmonary dysfunction in DMD.