Dystrophin Is Required for Appropriate Retrograde Control of Neurotransmitter Release at the Drosophila Neuromuscular Junction

Mutations in the human dystrophin gene cause the Duchenne and Becker muscular dystrophies. The Dystrophin protein provides a structural link between the muscle cytoskeleton and extracellular matrix to maintain muscle integrity. Recently, Dystrophin has also been found to act as a scaffold for severa...

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Veröffentlicht in:J Neurosci
Hauptverfasser: van der Plas, Mariska C., Pilgram, Gonneke S. K., Plomp, Jaap J., de Jong, Anja, Fradkin, Lee G., Noordermeer, Jasprina N.
Format: Artigo
Sprache:Inglês
Veröffentlicht: Society for Neuroscience 2006
Schlagworte:
Cellular/Molecular
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6674336/
https://ncbi.nlm.nih.gov/pubmed/16399704
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.4069-05.2006
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