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Wild type human TDP-43 potentiates ALS-linked mutant TDP-43 driven progressive motor and cortical neuron degeneration with pathological features of ALS.

Acta neuropathologica communications | 2015

Amyotrophic lateral sclerosis (ALS) is a relentlessly progressive neurodegenerative disorder, and cytoplasmic inclusions containing transactive response (TAR) DNA binding protein (TDP-43) are present in ~90 % of cases. Here we report detailed pathology in human TDP-43 transgenic mice that recapitulate key features of TDP-43-linked ALS.

Pubmed ID: 26108367 RIS Download

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None found

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Associated grants

  • Agency: Wellcome Trust, United Kingdom
    Id: 089701
  • Agency: Medical Research Council, United Kingdom
    Id: G0900635
  • Agency: Wellcome Trust, United Kingdom
    Id: 089701/Z/09/2
  • Agency: Medical Research Council, United Kingdom
    Id: G1100695
  • Agency: Medical Research Council, United Kingdom
    Id: MC_G1000733
  • Agency: Medical Research Council, United Kingdom
    Id: G0500289
  • Agency: Medical Research Council, United Kingdom
    Id: G0900688

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