Correction of Defective Protein Trafficking of a Mutant HERG Potassium Channel in Human Long QT Syndrome

This publication has 26 references indexed in Scilit:

• Defective aquaporin-2 trafficking in nephrogenic diabetes insipidus and correction by chemical chaperones.
  Journal of Clinical Investigation, 1998
• Mutations in the hminK gene cause long QT syndrome and suppress lKs function
  Nature Genetics, 1997
• The inward rectification mechanism of the HERG cardiac potassium channel
  Nature, 1996
• Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption
  Nature Genetics, 1996
• Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
  Nature Genetics, 1996
• Glycerol Reverses the Misfolding Phenotype of the Most Common Cystic Fibrosis Mutation
  Journal of Biological Chemistry, 1996
• A mechanistic link between an inherited and an acquird cardiac arrthytmia: HERG encodes the IKr potassium channel
  Cell, 1995
• A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
  Cell, 1995
• Protein Oligomerization In The Endoplasmic Reticulum
  Annual Review of Cell and Developmental Biology, 1989
• A Receptor-Mediated Pathway for Cholesterol Homeostasis
  Science, 1986