16-6-10　ⓔ文献

1) Harada M, Sakisaka S, et al: Role of ATP7B in biliary copper excretion in a human hepatoma cell line and normal rat hepatocytes. Gastroenterology, 2000; 118: 921–928.

2) Harada M, Sakisaka S, et al: Copper does not alter the intracellular distribution of ATP7B, a copper–transporting ATPase. Biochem Biophys Res Commun, 2000; 275: 871–876.

3) Harada M, Sakisaka S, et al: A mutation of the Wilson disease protein, ATP7B, is degraded in the proteasomes and forms protein aggregates. Gastroenterology, 2001; 120: 967–974.

4) Harada M, Kawaguchi T, et al: The Wilson disease protein ATP7B resides in the late endosomes with Rab7 and the Niemann–Pick C1 protein. Am J Pathol, 2005; 166: 499–510.

5) Yanagimoto C, Harada M, et al: Niemann–Pick C1 protein transports copper to the secretory compartment from late endosomes where ATP7B resides. Exp Cell Res, 2009; 315: 119–126.