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Nuclear pore pathology underlying multisystem proteinopathy type 3-related inclusion body myopathy.

Rumiko IzumiKensuke IkedaTetsuya NiihoriNaoki SuzukiMatsuyuki ShirotaRyo FunayamaKeiko NakayamaHitoshi WaritaMaki TateyamaYoko AokiMasashi Aoki
Published in: Annals of clinical and translational neurology (2023)
The shared subset of altered NUPs in amyotrophic lateral sclerosis (ALS), as demonstrated in prior research, HNRNPA1-mutated, and HNRNPA1-unlinked hIBM muscle tissues may provide evidence regarding the underlying common nuclear pore pathology of hIBM, ALS, and MSP.
Keyphrases
  • amyotrophic lateral sclerosis
  • gene expression
  • skeletal muscle
  • plasmodium falciparum
  • muscular dystrophy