XIAP is a copper binding protein deregulated in Wilson's disease and other copper toxicosis disorders

Molecular Cell

Volumn 21, Issue 6, 2006, Pages 775-785

  Mufti, Arjmand R ^a   Burstein, Ezra ^a,b   Csomos, Rebecca A ^a   Graf, Paul C F ^a   Wilkinson, John C ^a   Dick, Robert D ^a   Challa, Madhavi ^c   Son, Jae Kyoung ^c   Bratton, Shawn B ^c   Su, Grace L ^a   Brewer, George J ^a   Jakob, Ursula ^a   Duckett, Colin S ^a  

^a UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^b VA ANN ARBOR HEALTHCARE SYSTEM   (United States)

^c UNIVERSITY OF TEXAS AT AUSTIN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CASPASE 3; COPPER; X LINKED INHIBITOR OF APOPTOSIS;

APOPTOSIS; ARTICLE; COPPER METABOLISM; HUMAN; HUMAN CELL; INTOXICATION; METAL BINDING; PROTEIN DEGRADATION; WILSON DISEASE;

APOPTOSIS; CARRIER PROTEINS; CASPASE 3; CASPASES; CELL LINE; COPPER; ELECTROPHORETIC MOBILITY SHIFT ASSAY; HEPATOLENTICULAR DEGENERATION; HUMANS; INHIBITOR OF APOPTOSIS PROTEINS; MODELS, BIOLOGICAL; PROTEIN CONFORMATION; SIGNAL TRANSDUCTION; TRANSFECTION; X-LINKED INHIBITOR OF APOPTOSIS PROTEIN;

EID: 33644857818     PISSN: 10972765     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcel.2006.01.033     Document Type: Article

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