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mitochondrial iron ion transport

Known as: mitochondrial iron transport 
The directed movement of iron ions into, out of or within a mitochondrion. [GOC:jid, PMID:12006577]
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Compartmentalization of iron between mitochondria and the cytosol and its regulation.
Iron is essential for life. Its coordinated distribution between intracellular compartments and the adaptation of iron uptake to… Expand
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2015
2015
Mitoferrin modulates iron toxicity in a Drosophila model of Friedreich's ataxia.
Friedreich's ataxia is the most important recessive ataxia in the Caucasian population. Loss of frataxin expression affects the… Expand
Highly Cited
2012
Highly Cited
2012
MitoNEET-driven alterations in adipocyte mitochondrial activity reveal a crucial adaptive process that preserves insulin sensitivity in obesity
We examined mouse models with altered adipocyte expression of mitoNEET, a protein residing in the mitochondrial outer membrane… Expand
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Highly Cited
2009
Highly Cited
2009
A novel transferrin/TfR2-mediated mitochondrial iron transport system is disrupted in Parkinson's disease
More than 80 years after iron accumulation was initially described in the substantia nigra (SN) of Parkinson's disease (PD… Expand
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Highly Cited
2003
Highly Cited
2003
A Specific Role of the Yeast Mitochondrial Carriers Mrs3/4p in Mitochondrial Iron Acquisition under Iron-limiting Conditions*
The yeast genes MRS3 and MRS4 encode two members of the mitochondrial carrier family with high sequence similarity. To elucidate… Expand
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2002
2002
Role of mitochondrial carrier protein Mrs3/4 in iron acquisition and oxidative stress resistance of Cryptococcus neoformans.
Cryptococcus neoformans is a pathogenic basidiomycete that causes meningitis in immunocompromised patients. In this paper, we… Expand
Review
2000
Review
2000
Recent advances in the molecular pathogenesis of Friedreich ataxia.
Friedreich ataxia, the most frequent cause of recessive ataxia, is due in most cases to a homozygous intronic expansion resulting… Expand
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Review
2000
Review
2000
Friedreich's ataxia and iron metabolism
  • N. Gordon
  • Brain and Development
  • 2000
    • Corpus ID: 8890942
The possible causes of abnormal iron metabolism in patients with Friedreich's ataxia are considered. Reduced expression of a… Expand
Review
1998
Review
1998
Mitochondrial dysfunction in neurodegenerative diseases.
  • M. F. Beal
  • Biochimica et biophysica acta
  • 1998
    • Corpus ID: 54526400
A potential pivotal role for mitochondrial dysfunction in neurodegenerative diseases is gaining increasing acceptance… Expand
Highly Cited
1998
Highly Cited
1998
The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA gene
ABSTRACTMost cases of Friedreich ataxia (FRDA) are due to expansions of a GAA trinucleotide repeat sequence in the FRDA gene… Expand
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