Isoform-Specific Dominant-Negative Effects Associated with hERG1 G628S Mutation in Long QT Syndrome

مواد مشابهة

• Multiple splicing defects caused by hERG splice site mutation 2592+1G>A associated with long QT syndrome
  بواسطة: Stump, Matthew R., وآخرون
  منشور في: (2011)
• Position of Premature Termination Codons Determines Susceptibility of hERG mutations to Nonsense-Mediated mRNA Decay in Long QT Syndrome
  بواسطة: Gong, Qiuming, وآخرون
  منشور في: (2014)
• Inhibition of Nonsense-Mediated mRNA Decay by Antisense Morpholino Oligonucleotides Restores Functional Expression of hERG Nonsense and Frameshift Mutations in Long QT Syndrome
  بواسطة: Gong, Qiuming, وآخرون
  منشور في: (2010)
• Alternative Splicing and Polyadenylation Contribute to the Generation of hERG1 C-terminal Isoforms
  بواسطة: Gong, Qiuming, وآخرون
  منشور في: (2010)
• Mechanisms of pharmacological rescue of trafficking defective hERG mutant channels in human long QT syndrome
  بواسطة: Gong, Qiuming, وآخرون
  منشور في: (2005)