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ATP7A gene

Known as: ATPase copper transporting alpha, ATPase, Cu++ Transporting, Alpha Polypeptide (Menkes Syndrome) Gene, copper-transporting ATPase 1 
This gene is involved in copper transport.
National Institutes of Health

Papers overview

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Review
2015
Review
2015
ATP7A mutations impair copper metabolism resulting in three distinct genetic disorders in humans. These diseases are… Expand
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2015
2015
ATP7A is a P-type ATPase in which diverse mutations lead to X-linked recessive Menkes disease or occipital horn syndrome… Expand
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2014
2014
Copper‐transporting P‐type adenosine triphosphatase A (ATP7A) is associated with platinum drug resistance in non‐small cell lung… Expand
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2013
2013
ATP7A mediates copper absorption and feeds cuproenzymes in the trans-Golgi network. To regulate copper homeostasis, ATP7A cycles… Expand
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2011
2011
The copper-transporting ATPase ATP7A has an essential role in human physiology. ATP7A transfers the copper cofactor to… Expand
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Highly Cited
2010
Highly Cited
2010
Distal hereditary motor neuropathies comprise a clinically and genetically heterogeneous group of disorders. We recently mapped… Expand
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Highly Cited
2010
Highly Cited
2010
The copper-transporting P-type ATPases (Cu-ATPases), ATP7A and ATP7B, are essential for the regulation of intracellular copper… Expand
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2007
2007
We and others have shown that the copper transporters ATP7A and ATP7B play a role in cellular resistance to cis… Expand
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Highly Cited
2006
Highly Cited
2006
ATP7A is a P-type ATPase that transports copper from cytosol into the secretory pathway for loading onto cuproproteins or efflux… Expand
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Highly Cited
2004
Highly Cited
2004
Purpose: The goal of this study was to determine the effect of small changes in ATP7A expression on the pharmacodynamics of… Expand
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