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SLC11A2 gene

Known as: solute carrier family 11 member 2, SOLUTE CARRIER FAMILY 11 (PROTON-COUPLED DIVALENT METAL ION TRANSPORTER), MEMBER 2, DMT1 
National Institutes of Health

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2 relations
SLC2A11 genesolute carrier family 11- (proton-coupled divalent metal ion transporters), member 2

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2008
2008
[Differential expression of microRNAs in the aorta of spontaneously hypertensive rats].
MicroRNAs (miRNAs) are genomically encoded non-protein-encoding small RNAs, which negatively regulate target gene expression at… 
2008
2008
Over-expressed human divalent metal transporter 1 is involved in iron accumulation in MES23.5 cells
2007
2007
Lung injury after ozone exposure is iron dependent.
We tested the hypothesis that oxidative stress and biological effect after ozone (O3) exposure are dependent on changes in iron… 
Highly Cited
2006
Highly Cited
2006
Iron Imports. V. Transport of iron through the intestinal epithelium.
Iron absorption across the brush-border membrane requires divalent metal transporter 1 (DMT1), whereas ferroportin (FPN) and… 
2006
2006
Characterization of Gene Expression Profiles of Metallothionein-Null Cadmium-Resistant Cells
To understand metallothionein (MT)-independent mechanisms for cadmium (Cd) resistance in mammalian cells, we previously… 
2005
2005
Pharmacokinetics of pulmonary manganese absorption: evidence for increased susceptibility to manganese loading in iron-deficient rats.
High levels of airborne manganese can be neurotoxic, yet little is known about absorption of this metal via the lungs. Intestinal… 
Highly Cited
2004
Highly Cited
2004
Manganese toxicokinetics at the blood-brain barrier.
Increased manganese (Mn) use in manufacturing and in gasoline has raised concern about Mn-induced parkinsonism. Previous research… 
Highly Cited
2003
Highly Cited
2003
Nontransferrin-bound iron uptake by hepatocytes is increased in the Hfe knockout mouse model of hereditary hemochromatosis.
Hereditary hemochromatosis (HH) is an iron-overload disorder caused by a C282Y mutation in the HFE gene. In HH, plasma… 
2003
2003
[Increased DMT1 expression and iron content in MPTP-treated C57BL/6 mice].
Iron plays a key role in Parkinson s disease (PD). To illustrate the mechanism underlying the increase of iron in substantia… 
Highly Cited
1999
Highly Cited
1999
The effect of intracellular iron concentration and nitrogen monoxide on Nramp2 expression and non-transferrin-bound iron uptake.
Recent studies have demonstrated that the protein product (natural resistance associated macrophage protein 2, Nramp2) encoded by… 
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