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Published August 13, 2020 | Version 1.0.0
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Human and mouse ALS histopathological tissue sections co-stained for FUS, SFPQ, CHAT and DAPI

  • 1. Idiap Research Institute
  • 2. Francis Crick Institute
  • 3. University College London

Description

Multichannel microscopy data from histopathological sections of 

1/ SOD1- and VCP-mutant mouse models together with control co-stained for SFPQ, FUS, CHAT and DAPI

The moues folder contains 

2/ Healthy and sporadic ALS patients either co-stained for SFPQ or FUS together with CHAT and DAPI

These two series of multichannel fluorescent microscopy data have been used in  several manuscripts including:

  1. Luisier R, Tyzack GE, Hall CE, Mitchell JS, Devine H, Taha DM, et al. Intron retention and nuclear loss of SFPQ are molecular hallmarks of ALS. Nat Commun 2018; 9: 2010.
  2. Tyzack GE, Luisier R, Taha DM, Neeves J, Modic M, Mitchell JS, et al. Widespread FUS mislocalization is a molecular hallmark of amyotrophic lateral sclerosis. Brain 2019; 142: 2572–80.

 

 

Files

RawHumanImages.zip

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