Pathogenic TDP-43 in amyotrophic lateral sclerosis

This publication has 131 references indexed in Scilit:

• Regulation of TDP-43 phosphorylation in aging and disease
  GeroScience, 2021
• TDP-43 transports ribosomal protein mRNA to regulate axonal local translation in neuronal axons
  Acta Neuropathologica, 2020
• The Distinct Traits of the UNC13A Polymorphism in Amyotrophic Lateral Sclerosis
  Annals of Neurology, 2020
• Functional recovery in new mouse models of ALS/FTLD after clearance of pathological cytoplasmic TDP-43
  Acta Neuropathologica, 2015
• CDC7 inhibition blocks pathological TDP‐43 phosphorylation and neurodegeneration
  Annals of Neurology, 2013
• The RNA-binding motif 45 (RBM45) protein accumulates in inclusion bodies in amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration with TDP-43 inclusions (FTLD-TDP) patients
  Acta Neuropathologica, 2012
• High frequency ofTARDBPgene mutations in Italian patients with amyotrophic lateral sclerosis
  Human Mutation, 2009
• Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies
  Acta Neuropathologica, 2009
• Two German Kindreds With Familial Amyotrophic Lateral Sclerosis Due to TARDBP Mutations
  Archives of Neurology, 2008
• TDP‐43 mutation in familial amyotrophic lateral sclerosis
  Annals of Neurology, 2008