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4. Imaging of live transport can be done using various microscopes
but we recommend either scanning or spinning-disc confocal
with fast rate acquisition.
Acknowledgments
We thank Eric Kremer and members of the EKL group, G. Schiavo,
and G. Menendez for the microfl uidic chambers. S.S. is an Institut
National de la Santé et de la Recherche Médicale (INSERM
fellow). Work in the laboratory is funded by the European
Community's 7th Framework Programme (FP7/2007-2013;
grant 222992—BrainCAV), the French Agence National de la
Recherche, E-Rare, the Fondation de France and the Association
Française contre les Myopathies.
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