COMMD1 gene

Known as: Copper Metabolism (Murr1) Domain Containing 1 Gene, MGC27155, COPPER METABOLISM MURR1 DOMAIN-CONTAINING PROTEIN 1 
This gene is involved in the regulation of copper homeostasis, sodium uptake, and NF-kappa-B signaling.
National Institutes of Health

Papers overview

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2011
2011
The CFTR (cystic fibrosis transmembrane conductance regulator) protein is a large polytopic protein whose biogenesis is… (More)
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2010
2010
Stimulation of the NF-kappaB pathway can have proapoptotic or antiapoptotic consequences, and one mechanism that determines the… (More)
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2010
2010
The gene encoding COMM domain-containing 1 (COMMD1) is a prototypical member of the COMMD gene family that has been shown to… (More)
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2010
2010
Secretory clusterin (sCLU) is a stress-activated, cytoprotective chaperone that confers broad-spectrum cancer treatment… (More)
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Highly Cited
2009
Highly Cited
2009
The nuclear factor-kappaB (NF-kappaB) transcription factor system is a crucial component that controls several important… (More)
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Highly Cited
2007
Highly Cited
2007
NF-kappaB is a pleiotropic transcription factor involved in multiple processes, including inflammation and oncogenesis. We have… (More)
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Highly Cited
2007
Highly Cited
2007
COMMD1 (previously known as MURR1) belongs to a novel family of proteins termed the copper metabolism gene MURR1 domain (COMMD… (More)
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2007
2007
BACKGROUND & AIMS Wilson's disease (WD) is characterized by hepatic copper overload and caused by mutations in the gene encoding… (More)
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Review
2006
Review
2006
Wilson's disease (WD) is an inborn error of copper metabolism caused by a mutation to the copper-transporting gene ATP7B. The… (More)
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Highly Cited
2002
Highly Cited
2002
Domesticated animal species such as dogs and cats, with their many different characteristics and breed-specific diseases, and… (More)
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