File:Spatial-mapping-of-juxtacrine-axo-glial-interactions-identifies-novel-molecules-in-peripheral-ncomms9303-s8.ogv
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[edit]DescriptionSpatial-mapping-of-juxtacrine-axo-glial-interactions-identifies-novel-molecules-in-peripheral-ncomms9303-s8.ogv |
English: Supplementary Movie 1 Z-stack from Schwann cells extending pseudopods toward axonal membranes. Reconstruction through the z-axis of Schwann cells extending pseudopods through 3 μm pores of a microporous Boyden chamber filter in response to neuronal membranes. Note the thickness of the filter around 5-6 μm. Schwann cells were exposed to neuronal membranes for 2 h, fixed then stained with TRITC-phalloidin and DAPI. |
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Source | Video file from Poitelon Y, Bogni S, Matafora V, Della-Flora Nunes G, Hurley E, Ghidinelli M, Katzenellenbogen B, Taveggia C, Silvestri N, Bachi A, Sannino A, Wrabetz L, Feltri M (2015). "Spatial mapping of juxtacrine axo-glial interactions identifies novel molecules in peripheral myelination". Nature Communications. DOI:10.1038/ncomms9303. PMID 26383514. PMC: 4576721. | ||
Author | Poitelon Y, Bogni S, Matafora V, Della-Flora Nunes G, Hurley E, Ghidinelli M, Katzenellenbogen B, Taveggia C, Silvestri N, Bachi A, Sannino A, Wrabetz L, Feltri M | ||
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![]() ![]() This file is licensed under the Creative Commons Attribution 4.0 International license.
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 02:09, 31 October 2016 | 23 s, 1,920 × 1,080 (3.62 MB) | Open Access Media Importer Bot (talk | contribs) | Automatically uploaded media file from Open Access source. Please report problems or suggestions here. |
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Short title | Supplementary Movie 1 |
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Author | Poitelon Y, Bogni S, Matafora V, Della-Flora Nunes G, Hurley E, Ghidinelli M, Katzenellenbogen B, Taveggia C, Silvestri N, Bachi A, Sannino A, Wrabetz L, Feltri M |
Usage terms | http://creativecommons.org/licenses/by/4.0/ |
Image title | Z-stack from Schwann cells extending pseudopods toward axonal membranes. Reconstruction through the z-axis of Schwann cells extending pseudopods through 3 μm pores of a microporous Boyden chamber filter in response to neuronal membranes. Note the thickness of the filter around 5-6 μm. Schwann cells were exposed to neuronal membranes for 2 h, fixed then stained with TRITC-phalloidin and DAPI. |
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Date and time of digitizing | 2015-09-18 |