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

Benzer Materyaller

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