File:A-hereditary-spastic-paraplegia-mutation-in-kinesin-1AKIF5A-disrupts-neurofilament-transport-1750-1326-5-52-S4.ogv

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A-hereditary-spastic-paraplegia-mutation-in-kinesin-1AKIF5A-disrupts-neurofilament-transport-1750-1326-5-52-S4.ogv ‎(Ogg Theora video file, length 18 s, 512 × 210 pixels, 356 kbps, file size: 787 KB)

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English: Movie showing neurofilament movement in a neuron co-expressing GFP-NFM and N256S-kinesin-1A. A gap in the axonal neurofilament array of a cortical neuron co-expressing GFP-NFM and N256S-kinesin-1A. Some jiggling movement is apparent at the edges of the gap, but no filaments move into the gap. Proximal is left and distal is right. Width of field of view: 67 μm. Time compression: 40:1
Date
Source Wang L, Brown A (2010). "A hereditary spastic paraplegia mutation in kinesin-1A/KIF5A disrupts neurofilament transport". Molecular Neurodegeneration. DOI:10.1186/1750-1326-5-52. PMID 21087519. PMC: 3000839.
Author Wang L, Brown A
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Date/TimeThumbnailDimensionsUserComment
current02:22, 20 November 201218 s, 512 × 210 (787 KB)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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Format Bitrate Download Status Encode time
VP9 240P 32 kbps Completed 23:49, 15 August 2018 5.0 s
Streaming 240p (VP9) 32 kbps Completed 06:44, 9 December 2023 1.0 s
WebM 360P 62 kbps Completed 13:24, 16 November 2023 1.0 s
Streaming 144p (MJPEG) 116 kbps Completed 10:11, 29 October 2023 1.0 s

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