Interaction with Polyglutamine Aggregates Reveals a Q/N-rich Domain in TDP-43

This publication has 77 references indexed in Scilit:

• TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration
  Proceedings of the National Academy of Sciences, 2009
• Aberrant cleavage of TDP-43 enhances aggregation and cellular toxicity
  Proceedings of the National Academy of Sciences, 2009
• Rethinking ALS: The FUS about TDP-43
  Cell, 2009
• Polyglutamine neurodegeneration: protein misfolding revisited
  Trends in Neurosciences, 2008
• TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis
  The Lancet Neurology, 2008
• TDP-43 regulates retinoblastoma protein phosphorylation through the repression of cyclin-dependent kinase 6 expression
  Proceedings of the National Academy of Sciences, 2008
• Mutant Huntingtin reduces HSP70 expression through the sequestration of NF‐Y transcription factor
  The EMBO Journal, 2008
• TDP‐43 A315T mutation in familial motor neuron disease
  Annals of Neurology, 2008
• Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death
  Nature, 2004
• Polyglutamine protein aggregates are dynamic
  Nature Cell Biology, 2002