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Wilson disease protein

Known as: Copper-transporting ATPase 2, ATP7B Cu-binding P type ATPase, ATPase, Cu++ transporting, beta polypeptide (Wilson disease) 
 
National Institutes of Health

Papers overview

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2015
2015
Copper (Cu) is an essential trace element but toxic in free form. After cell uptake, Cu is transferred, via direct protein… Expand
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2007
2007
Wilson disease (WD) is a genetic disorder of copper metabolism associated with severe hepatic, neurological, and psychiatric… Expand
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2004
2004
The Wilson disease protein (WND) is a transport ATPase involved in copper delivery to the secretory pathway. Mutations in WND and… Expand
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2004
2004
Copper transport by the P1-ATPase ATP7B, or Wilson disease protein (WNDP),1 is essential for human metabolism. Perturbation of… Expand
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2004
2004
FK506-binding protein 52 (FKBP52) is an immunophilin that possesses peptidylprolyl cis/trans-isomerase (PPIase) activity and is a… Expand
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