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SLC39A4 gene

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

Papers overview

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Highly Cited
2012
Highly Cited
2012
Mutations in the human Zip4 gene cause acrodermatitis enteropathica, a rare, pseudo-dominant, lethal genetic disorder. We created… Expand
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Highly Cited
2009
Highly Cited
2009
The zinc transporter ZIP4 (SLC39A4) is mutated in humans with the rare, autosomal recessive genetic disease acrodermatitis… Expand
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Highly Cited
2008
Highly Cited
2008
Meiotic crossing-over is highly regulated such that each homolog pair typically receives at least one crossover (assurance) and… Expand
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Highly Cited
2007
Highly Cited
2007
In budding yeast meiosis, the formation of class I interference-sensitive crossovers requires the ZMM proteins. These ZMM… Expand
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Highly Cited
2007
Highly Cited
2007
Abstract Dietary zinc deficiency in mice is accompanied by enhanced expression of the zinc uptake transporter Slc39a4 (Zip4) and… Expand
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Highly Cited
2007
Highly Cited
2007
The human Zip4 gene (Slc39a4) is mutated in the rare recessive genetic disorder of zinc metabolism acrodermatitis enteropathica… Expand
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Highly Cited
2007
Highly Cited
2007
There is clinical evidence linking asthma with the trace element, zinc (Zn). Using a mouse model of allergic inflammation, we… Expand
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Highly Cited
2006
Highly Cited
2006
We have characterized Zip4 (a.k.a. Spo22), a meiosis-specific protein essential for chromosome synapsis in budding yeast. In the… Expand
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Highly Cited
2005
Highly Cited
2005
Zip2 and Zip3 are meiosis-specific proteins that, in collaboration with several partners, act at the sites of crossover… Expand
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Highly Cited
1998
Highly Cited
1998
Millions of people worldwide suffer from nutritional imbalances of essential metals like zinc. These same metals, along with… Expand
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