SLC39A4 gene

Known as: solute carrier family 39 member 4, ZIP4, AWMS2 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2002-2016
024620022016

Papers overview

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2014
2014
Extreme differences in allele frequency between West Africans and Eurasians were observed for a leucine-to-valine substitution… (More)
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2013
2013
BACKGROUND Dysregulated zinc transport has been observed in many cancers. However, the status of zinc homeostasis and the… (More)
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2013
2013
Changes in the intracellular levels of the essential micronutrient zinc have been implicated in multiple diseases including… (More)
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2010
2010
Acrodermatitis enteropathica (AE) is an autosomal recessive disorder with the clinical triad of acral dermatitis, diarrhea and… (More)
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2009
2009
The zinc transporter ZIP4 (SLC39A4) is mutated in humans with the rare, autosomal recessive genetic disease acrodermatitis… (More)
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Highly Cited
2007
Highly Cited
2007
Zinc is an essential trace element and catalytic/structural component used by many metalloenzymes and transcription factors… (More)
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2007
2007
Zinc is an essential nutrient. Genetic evidence for this nutritional requirement in humans is the zinc deficiency disease… (More)
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Highly Cited
2004
Highly Cited
2004
The ZIP5 gene encodes a protein closely related to ZIP4, a zinc transporter mutated in the human genetic disorder acrodermatitis… (More)
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2003
2003
Acrodermatitis enteropathica is rare autosomal recessive disorder characterized by a severe nutritional zinc deficiency. We and… (More)
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Highly Cited
2002
Highly Cited
2002
We have characterized the human gene SLC39A4, which encodes a protein with features characteristic of a ZIP zinc transporter. The… (More)
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