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The Wilson Disease Protein ATP7B Resides in the Late Endosomes with Rab7 and the Niemann-Pick C1 Protein

Wilson disease is a genetic disorder characterized by the accumulation of copper in the body due to a defect of biliary copper excretion. Although the Wilson disease gene has been cloned, the cellular localization of the gene product (ATP7B) has not been fully clarified. Therefore, the precise physi...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Harada, Masaru, Kawaguchi, Takumi, Kumemura, Hiroto, Terada, Kunihiko, Ninomiya, Haruaki, Taniguchi, Eitaro, Hanada, Shinichiro, Baba, Shinji, Maeyama, Michiko, Koga, Hironori, Ueno, Takato, Furuta, Koh, Suganuma, Tatsuo, Sugiyama, Toshihiro, Sata, Michio
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: American Society for Investigative Pathology 2005
Θέματα:
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1602322/
https://ncbi.nlm.nih.gov/pubmed/15681833
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