Analysis of Four Connexin26 Mutant Gap Junctions and Hemichannels Reveals Variations in Hexamer Stability

This publication has 30 references indexed in Scilit:

• Connexin channels and phospholipids: association and modulation
  BMC Biology, 2009
• Oculodentodigital dysplasia with mandibular retrognathism and absence of syndactyly: a case report with a novel mutation in the Connexin 43 gene
  International Journal of Oral & Maxillofacial Surgery, 2007
• Clustal W and Clustal X version 2.0
  Bioinformatics, 2007
• Three-dimensional structure of a human connexin26 gap junction channel reveals a plug in the vestibule
  Proceedings of the National Academy of Sciences, 2007
• Loss of function and impaired degradation of a cataract-associated mutant connexin50
  European Journal of Cell Biology, 2003
• Loss‐of‐function and residual channel activity of connexin26 mutations associated with non‐syndromic deafness
  FEBS Letters, 2002
• Identification of amino acid residues lining the pore of a gap junction channel
  The Journal of cell biology, 2002
• Human connexin26 (GJB2) deafness mutations affect the function of gap junction channels at different levels of protein expression.
  Human Genetics, 2002
• Isolation and characterization of gap junctions from tissue culture cells
  Journal of Molecular Biology, 2002
• Multisubunit assembly of an integral plasma membrane channel protein, gap junction connexin43, occurs after exit from the ER
  Cell, 1993