Congenital myasthenia–related AChR δ subunit mutation interferes with intersubunit communication essential for channel gating

Lignende værker

• Mutation causing severe myasthenia reveals functional asymmetry of AChR signature cystine loops in agonist binding and gating
  af: Shen, Xin-Ming, et al.
  Udgivet: (2003)
• Mutation causing congenital myasthenia reveals acetylcholine receptor β/δ subunit interaction essential for assembly
  af: Quiram, Polly A., et al.
  Udgivet: (1999)
• Slow‐channel myasthenia due to novel mutation in M2 domain of AChR delta subunit
  af: Shen, Xin‐Ming, et al.
  Udgivet: (2019)
• Investigation of Congenital Myasthenia Reveals Functional Asymmetry of Invariant Acetylcholine Receptor (AChR) Cys-loop Aspartates
  af: Shen, Xin-Ming, et al.
  Udgivet: (2016)
• Mutations causing slow-channel myasthenia reveal that a valine ring in the channel pore of muscle AChR is optimized for stabilizing channel gating
  af: Shen, Xin-Ming, et al.
  Udgivet: (2016)