Nuclear localization of SMN and FUS is not altered in fibroblasts from patients with sporadic ALS

Lignende værker

• Mutant superoxide dismutase 1 (SOD1), a cause of amyotrophic lateral sclerosis, disrupts the recruitment of SMN, the spinal muscular atrophy protein to nuclear Cajal bodies
  af: Kariya, Shingo, et al.
  Udgivet: (2012)
• FUS is sequestered in nuclear aggregates in ALS patient fibroblasts
  af: Schwartz, Jacob C., et al.
  Udgivet: (2014)
• Bioenergetic markers in skin fibroblasts of sporadic ALS and PLS patients
  af: Kirk, Kathryne, et al.
  Udgivet: (2014)
• Necroptosis drives motor neuron death in models of both sporadic and familial ALS
  af: Re, Diane B., et al.
  Udgivet: (2014)
• FUS mutations in sporadic amyotrophic lateral sclerosis
  af: Lai, Shiao-Lin, et al.
  Udgivet: (2010)