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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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2020
2020
Objectives Primary copper-associated hepatopathy (PCH) has been reported in young cats. Although our group recently reported a… 
2020
2020
Wilson disease (WD) is an autosomal recessive disorder of copper transport caused by inherited defects in the ATP7B gene and… 
2019
2019
Ruthenium(II/III) complexes are predicted to be efficient alternatives to platinum drug-resistant cancers but have never been… 
2016
2016
Meta-analyses show that serum copper non-boundto-ceruloplasmin (non-Cp-Cu) is higher in patients with Alzheimer’s disease (AD… 
2014
2014
2014
Background: Copper regulates the intracellular localization of a copper transporter ATP7B; the molecular mechanism of this… 
2011
2011
OBJECTIVES The objective of this study was to characterise Wilson's Disease (WD) [OMIM 277900] genetically and test for allelic… 
2011
2011
ATP7B is a P-type ATPase involved in copper transport and homeostasis. In experiments with microsomes isolated from COS-1 cells… 
2003
2003
Objective To study the expression of normal and variant ATP7B proteins, in order to further find the mechanism of Wilson disease… 
1995
1995
ATP7B, the gene altered in Wilson disease (WD) patients, lies in a block of homology shared between human chromosome 13q14 and…