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Fig. 1
Microscope confocal droit - Leica SP2 AOBS
Microscope confocal inversé - Zeiss LSM 510 Meta
Microscope L5D à déconvolution
Microscope 3D à déconvolution 1
Microscope 3D à déconvolution 2
Vidéo-microscope poste 1
Vidéo-microscope poste 2
Vidéo-microscope poste 3
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cellule en mitose sur un micro-patron adhésif
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Electron microscope
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Zeiss LSM 510 Meta
L5D deconvolution microscope
Leica SP2 AOBS
Video-microscope station 1
Video-microscope station 2
Video-microscope station 3
3D deconvolution microscope 1
3D deconvolution microscope 2
Microscope électronique
Bruno Goud
cellule souche
Pr Daniel Louvard
microscope_confocal
micro_injection
transgenese
microscopie_numerique
logo CNRS
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Evelyne Coudrier
Mithieu Piel
Tran-Paoletti Lab
Tran-Paoletti Lab
Group leader Positions
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Fig 3.
Fig1. Model pour la fonction des moteurs moléculaires dans le trafic intracellulaire
Curie international course. 1st Course on cytoskeleton: Actin based motility
testimage
Figure 1
Figure 2
Curie international course. 2nd Course on cytoskeleton: Cytoskeleton in cell division and migration
Curie international course. 3rd Course on cytoskeleton: Cytoskeleton and membrane trafficking
Curie international course. 4th Course on cytoskeleton: Cytoskeleton in cell division and migration
Figure 1. Actin cytoskeleton in cell invasion.
Figure 2. Actin cytoskeleton in cell migration.
Figure 3. Cooperation of CAFs and cancer cells in invasion.
5th course on cytoskeleton: Cytoskeleton in cell organization
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