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Iron-sulfur cluster biogenesis and human disease
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
18606475
retrieved
3 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
Iron-sulfur cluster biogenesis and human disease
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
18606475
retrieved
3 August 2017
main subject
iron
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author name string
Tracey A Rouault
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
18606475
retrieved
3 August 2017
Wing Hang Tong
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
18606475
retrieved
3 August 2017
publication date
5 July 2008
1 reference
stated in
Europe PubMed Central
PubMed ID
18606475
retrieved
3 August 2017
published in
Trends in Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
18606475
retrieved
3 August 2017
volume
24
1 reference
stated in
Europe PubMed Central
PubMed ID
18606475
retrieved
3 August 2017
issue
8
1 reference
stated in
Europe PubMed Central
PubMed ID
18606475
retrieved
3 August 2017
page(s)
398-407
1 reference
stated in
Europe PubMed Central
PubMed ID
18606475
retrieved
3 August 2017
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Hydrogen peroxide scavenging rescues frataxin deficiency in a Drosophila model of Friedreich's ataxia
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Mitochondrial Iba57p is required for Fe/S cluster formation on aconitase and activation of radical SAM enzymes
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Formation and properties of [4Fe-4S] clusters on the IscU scaffold protein
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The Cfd1-Nbp35 complex acts as a scaffold for iron-sulfur protein assembly in the yeast cytosol
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Structure of dual function iron regulatory protein 1 complexed with ferritin IRE-RNA
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The DNA repair helicases XPD and FancJ have essential iron-sulfur domains
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Congenital sideroblastic anemias.
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7 July 2018
Functions of mitochondrial ISCU and cytosolic ISCU in mammalian iron-sulfur cluster biogenesis and iron homeostasis
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7 July 2018
The mitochondrial ATP-binding cassette transporter Abcb7 is essential in mice and participates in cytosolic iron-sulfur cluster biogenesis.
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7 July 2018
Crystal structure of human iron regulatory protein 1 as cytosolic aconitase
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7 July 2018
Mitochondrial iron detoxification is a primary function of frataxin that limits oxidative damage and preserves cell longevity
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The Nfs1 interacting protein Isd11 has an essential role in Fe/S cluster biogenesis in mitochondria
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7 July 2018
Essential role of Isd11 in mitochondrial iron-sulfur cluster synthesis on Isu scaffold proteins
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7 July 2018
The essential WD40 protein Cia1 is involved in a late step of cytosolic and nuclear iron-sulfur protein assembly
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7 July 2018
A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine
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7 July 2018
Frataxin deficiency alters heme pathway transcripts and decreases mitochondrial heme metabolites in mammalian cells.
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Deficiency of glutaredoxin 5 reveals Fe-S clusters are required for vertebrate haem synthesis
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Extra-mitochondrial localisation of frataxin and its association with IscU1 during enterocyte-like differentiation of the human colon adenocarcinoma cell line Caco-2.
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7 July 2018
Structure, function, and formation of biological iron-sulfur clusters
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7 July 2018
Microcytic anemia, erythropoietic protoporphyria, and neurodegeneration in mice with targeted deletion of iron-regulatory protein 2
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7 July 2018
Iron-sulphur cluster biogenesis and mitochondrial iron homeostasis
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7 July 2018
The hydrogenase-like Nar1p is essential for maturation of cytosolic and nuclear iron-sulphur proteins
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7 July 2018
Ultrastructural features of bone marrow cells from patients with acquired sideroblastic anemia
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7 July 2018
HEREDITARY METABOLIC MYOPATHY WITH PAROXYSMAL MYOGLOBINURIA DUE TO ABNORMAL GLYCOLYSIS
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7 July 2018
A novel eukaryotic factor for cytosolic Fe-S cluster assembly
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7 July 2018
Components involved in assembly and dislocation of iron-sulfur clusters on the scaffold protein Isu1p
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7 July 2018
Identification of a novel candidate gene in the iron-sulfur pathway implicated in ataxia-susceptibility: human gene encoding HscB, a J-type co-chaperone
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7 July 2018
Subcellular compartmentalization of human Nfu, an iron-sulfur cluster scaffold protein, and its ability to assemble a [4Fe-4S] cluster
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7 July 2018
Friedreich's ataxia: clinical aspects and pathogenesis
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7 July 2018
Functional profiling of the Saccharomyces cerevisiae genome
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7 July 2018
Grx5 is a mitochondrial glutaredoxin required for the activity of iron/sulfur enzymes
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7 July 2018
Ferredoxin reductase affects p53-dependent, 5-fluorouracil-induced apoptosis in colorectal cancer cells
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7 July 2018
An essential function of the mitochondrial sulfhydryl oxidase Erv1p/ALR in the maturation of cytosolic Fe/S proteins
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7 July 2018
Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits
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A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13.
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7 July 2018
Mitochondrial control of iron homeostasis. A genome wide analysis of gene expression in a yeast frataxin-deficient strain
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7 July 2018
Distinct iron-sulfur cluster assembly complexes exist in the cytosol and mitochondria of human cells
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7 July 2018
Yeast mitochondrial protein, Nfs1p, coordinately regulates iron-sulfur cluster proteins, cellular iron uptake, and iron distribution
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7 July 2018
Evidence for a conserved system for iron metabolism in the mitochondria of Saccharomyces cerevisiae
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7 July 2018
The mitochondrial proteins Atm1p and Nfs1p are essential for biogenesis of cytosolic Fe/S proteins
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7 July 2018
Targeting of a human iron-sulfur cluster assembly enzyme, nifs, to different subcellular compartments is regulated through alternative AUG utilization
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7 July 2018
Mt-Hsp70 homolog, Ssc2p, required for maturation of yeast frataxin and mitochondrial iron homeostasis
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7 July 2018
Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia
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7 July 2018
NBP35 encodes an essential and evolutionary conserved protein in Saccharomyces cerevisiae with homology to a superfamily of bacterial ATPases
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7 July 2018
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion
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7 July 2018
Deficiency of skeletal muscle succinate dehydrogenase and aconitase. Pathophysiology of exercise in a novel human muscle oxidative defect
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7 July 2018
Mitochondrial frataxin interacts with ISD11 of the NFS1/ISCU complex and multiple mitochondrial chaperones.
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26 October 2018
Progressive GAA expansions in dorsal root ganglia of Friedreich's ataxia patients.
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Iron and iron-responsive proteins in the cardiomyopathy of Friedreich's ataxia
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Reduction of Caenorhabditis elegans frataxin increases sensitivity to oxidative stress, reduces lifespan, and causes lethality in a mitochondrial complex II mutant
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2574672
retrieved
26 October 2018
A third locus for dominant optic atrophy on chromosome 22q.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2574672
retrieved
26 October 2018
Friedreich ataxia: the oxidative stress paradox
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2574672
retrieved
26 October 2018
The Arabidopsis chloroplastic NifU-like protein CnfU, which can act as an iron-sulfur cluster scaffold protein, is required for biogenesis of ferredoxin and photosystem I.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2574672
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26 October 2018
Altered body iron distribution and microcytosis in mice deficient in iron regulatory protein 2 (IRP2)
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2574672
retrieved
9 December 2018
RNA silencing of the mitochondrial ABCB7 transporter in HeLa cells causes an iron-deficient phenotype with mitochondrial iron overload
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18606475
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Myopathy with lactic acidosis is linked to chromosome 12q23.3-24.11 and caused by an intron mutation in the ISCU gene resulting in a splicing defect
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18606475
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
MDL1 is a high copy suppressor of ATM1: evidence for a role in resistance to oxidative stress
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18606475
retrieved
12 December 2020
based on heuristic
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Identifiers
DOI
10.1016/J.TIG.2008.05.008
1 reference
stated in
Europe PubMed Central
PubMed ID
18606475
retrieved
3 August 2017
PMCID
2574672
1 reference
stated in
Europe PubMed Central
PubMed ID
18606475
retrieved
3 August 2017
PubMed ID
18606475
1 reference
stated in
Europe PubMed Central
PubMed ID
18606475
retrieved
3 August 2017
ResearchGate publication ID
5245470
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