Functional alterations in gap junction channels formed by mutant forms of connexin 32: evidence for loss of function as a pathogenic mechanism in the X-linked form of Charcot-Marie-Tooth disease

Ítems similars

• Pathogenesis of X-Linked Charcot-Marie-Tooth Disease: Differential Effects of Two Mutations in Connexin 32
  per: Abrams, Charles K., et al.
  Publicat: (2003)
• Voltage opens unopposed gap junction hemichannels formed by a connexin 32 mutant associated with X-linked Charcot-Marie-Tooth disease
  per: Abrams, C. K., et al.
  Publicat: (2002)
• Molecular Determinants of Electrical Rectification of Single Channel Conductance in Gap Junctions Formed by Connexins 26 and 32
  per: Oh, Seunghoon, et al.
  Publicat: (1999)
• Functional Requirement for a Highly Conserved Charged Residue at Position 75 in the Gap Junction Protein Connexin 32
  per: Abrams, Charles K., et al.
  Publicat: (2013)
• Stoichiometry of Transjunctional Voltage–Gating Polarity Reversal by a Negative Charge Substitution in the Amino Terminus of a Connexin32 Chimera
  per: Oh, Seunghoon, et al.
  Publicat: (2000)