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ATP7B gene

Known as: ATP7B, ATPase, Cu(2+)-TRANSPORTING, BETA POLYPEPTIDE, ATPase copper transporting beta 
National Institutes of Health

Papers overview

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Highly Cited
2016
Highly Cited
2016
Background: Wilson's disease (WD) is an autosomal recessive disorder of copper metabolism caused by ATP7B pathogenic mutations… 
Review
2014
Review
2014
Wilson's disease (WD) is a human disorder of copper homeostasis caused by mutations in the copper‐transporting ATPase ATP7B. WD… 
Review
2013
Review
2013
Over the past two decades there have been significant advances in our understanding of copper homeostasis and the pathological… 
Highly Cited
2013
Highly Cited
2013
Reports of hepatobiliary malignancies in Wilson disease are sparse. The aim of this study was to evaluate hepatobiliary… 
2010
2010
ATP7B is a P-type ATPase involved in copper transport and homeostasis. In experiments with microsomes isolated from COS-1 cells… 
Highly Cited
2001
Highly Cited
2001
One of the most important clinical problems in the treatment of human solid carcinoma is the intrinsic/acquired resistance…