Abnormal accumulation of prion protein mRNA in muscle fibers of patients with sporadic inclusion-body myositis and hereditary inclusion-body myopathy.

Lignende værker

• Activation of the Unfolded Protein Response in Sporadic Inclusion Body Myositis But Not in Hereditary GNE Inclusion Body Myopathy
  af: Nogalska, Anna, et al.
  Udgivet: (2015)
• Light and electron microscopic immunolocalization of presenilin 1 in abnormal muscle fibers of patients with sporadic inclusion-body myositis and autosomal-recessive inclusion-body myopathy.
  af: Askanas, V., et al.
  Udgivet: (1998)
• Increased BACE1 mRNA and noncoding BACE1-antisense transcript in sporadic inclusion body myositis muscle fibers – possibly caused by endoplasmic reticulum stress
  af: Nogalska, Anna, et al.
  Udgivet: (2010)
• Pathological findings in sporadic inclusion body myositis and GNE myopathy
  af: Zhang, Yutong, et al.
  Udgivet: (2018)
• Impaired Autophagy in Sporadic Inclusion-Body Myositis and in Endoplasmic Reticulum Stress-Provoked Cultured Human Muscle Fibers
  af: Nogalska, Anna, et al.
  Udgivet: (2010)