All Stories

  1. Mice with endogenous TDP‐43 mutations exhibit gain of splicing function and characteristics of amyotrophic lateral sclerosis
  2. TDP-43 post-translational modifications in health and disease
  3. Altered TDP-43-dependent splicing in HSPB8 -related distal hereditary motor neuropathy and myofibrillar myopathy
  4. Novel splice-switching oligonucleotide promotesBRCA1aberrant splicing and susceptibility to PARP inhibitor action
  5. Neurodegeneration and RNA-binding proteins
  6. proteins involved in ALS and frontotemporal dementia
  7. The minor spliceosome could be the major key for FUS/TLS mutants in ALS