Genetic, metabolic and cellular factors influencing intracellular localization of the Wilson disease protein, ATP7B

Gelijkaardige items

• Cellular copper levels determine the phenotype of the Arg(875) variant of ATP7B/Wilson disease protein
  door: Gupta, Arnab, et al.
  Gepubliceerd in: (2011)
• CELL-SPECIFIC TRAFFICKING SUGGESTS A NEW ROLE FOR RENAL ATP7B IN THE INTRACELLULAR COPPER STORAGE
  door: Barnes, Natalie, et al.
  Gepubliceerd in: (2009)
• Human copper transporter ATP7B (Wilson disease protein) forms stable dimers in vitro and in cells
  door: Jayakanthan, Samuel, et al.
  Gepubliceerd in: (2017)
• A structural model of the copper ATPase ATP7B to facilitate analysis of Wilson disease-causing mutations and studies of the transport mechanism
  door: Schushan, Maya, et al.
  Gepubliceerd in: (2012)
• Distinct phenotype of a Wilson disease mutation reveals a novel trafficking determinant in the copper transporter ATP7B
  door: Braiterman, Lelita T., et al.
  Gepubliceerd in: (2014)