Cellular copper levels determine the phenotype of the Arg875 variant of ATP7B/Wilson disease protein

Proceedings of the National Academy of Sciences of the United States of America

Volumn 108, Issue 13, 2011, Pages 5390-5395

  Gupta, Arnab ^a   Bhattacharjee, Ashima ^a   Dmitriev, Oleg Y ^c   Nokhrin, Sergiy ^c   Braiterman, Lelita ^b   Hubbard, Ann L ^b   Lutsenko, Svetlana ^a  

^a JOHNS HOPKINS UNIVERSITY   (United States)

^b JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF SASKATCHEWAN   (Canada)

Author keywords

Cisplatin; Phenotypic variability; Trafficking

Indexed keywords

ATP7B ENZYME; COPPER; COPPER EXPORTING ADENOSINE TRIPHOSPHATASE; UNCLASSIFIED DRUG;

CONFERENCE PAPER; DNA POLYMORPHISM; ENDOPLASMIC RETICULUM; GENETIC VARIABILITY; HUMAN; HUMAN CELL; PHENOTYPE; PRIORITY JOURNAL; PROTEIN LOCALIZATION; TRANS GOLGI NETWORK;

EID: 79955101962     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1014959108     Document Type: Article

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