VCP Mutations Causing Frontotemporal Lobar Degeneration Disrupt Localization of TDP-43 and Induce Cell Death

This publication has 79 references indexed in Scilit:

• TDP‐43 A315T mutation in familial motor neuron disease
  Annals of Neurology, 2008
• Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia
  Human Mutation, 2008
• Decreased ER-associated degradation of α-TCR induced by Grp78 depletion with the SubAB cytotoxin
  The International Journal of Biochemistry & Cell Biology, 2008
• HSP105 interacts with GRP78 and GSK3 and promotes ER stress-induced caspase-3 activation
  Cellular Signalling, 2007
• Characterization of an ERAD Pathway for Nonglycosylated BiP Substrates, which Require Herp
  Molecular Cell, 2007
• A Golgi fragmentation pathway in neurodegeneration
  Neurobiology of Disease, 2007
• Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration
  Acta Neuropathologica, 2007
• Transient arrest in proteasomal degradation during inhibition of translation in the unfolded protein response
  Biochemical Journal, 2007
• HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin‐positive, tau‐negative inclusions caused by a missense mutation in the signal peptide of progranulin
  Annals of Neurology, 2006
• Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
  Nature Genetics, 2004