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Abnormal iron homeostasis and neurodegeneration
scientific article published on 30 July 2013
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scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
3726993
retrieved
18 August 2017
title
Abnormal iron homeostasis and neurodegeneration
(English)
1 reference
stated in
Europe PubMed Central
PMCID
3726993
retrieved
18 August 2017
main subject
neurodegeneration
1 reference
based on heuristic
inferred from title
author name string
Barry B Muhoberac
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
3726993
retrieved
18 August 2017
Ruben Vidal
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
3726993
retrieved
18 August 2017
publication date
30 July 2013
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stated in
Europe PubMed Central
PMCID
3726993
retrieved
18 August 2017
published in
Frontiers in Aging Neuroscience
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stated in
Europe PubMed Central
PMCID
3726993
retrieved
18 August 2017
volume
5
1 reference
stated in
Europe PubMed Central
PMCID
3726993
retrieved
18 August 2017
page(s)
32
1 reference
stated in
Europe PubMed Central
PMCID
3726993
retrieved
18 August 2017
cites work
Metallostasis in Alzheimer's disease.
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29 September 2017
A mutant light-chain ferritin that causes neurodegeneration has enhanced propensity toward oxidative damage.
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PubMed Central
reference URL
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29 September 2017
H2O2: a dynamic neuromodulator
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PubMed Central
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29 September 2017
Unraveling the biological roles of reactive oxygen species
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PubMed Central
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29 September 2017
Abnormal iron metabolism in fibroblasts from a patient with the neurodegenerative disease hereditary ferritinopathy
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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=3726993
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29 September 2017
Iron loading-induced aggregation and reduction of iron incorporation in heteropolymeric ferritin containing a mutant light chain that causes neurodegeneration
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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=3726993
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29 September 2017
Accumulation of oxidative DNA damage in brain mitochondria in mouse model of hereditary ferritinopathy
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PubMed Central
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29 September 2017
X-ray structures of ferritins and related proteins
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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=3726993
retrieved
29 September 2017
Unraveling of the E-helices and disruption of 4-fold pores are associated with iron mishandling in a mutant ferritin causing neurodegeneration
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=3726993
retrieved
29 September 2017
Abnormal iron metabolism and oxidative stress in mice expressing a mutant form of the ferritin light polypeptide gene
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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=3726993
retrieved
29 September 2017
Iron-mediated aggregation and a localized structural change characterize ferritin from a mutant light chain polypeptide that causes neurodegeneration.
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=3726993
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29 September 2017
T2* and FSE MRI distinguishes four subtypes of neurodegeneration with brain iron accumulation
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726993
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29 September 2017
Expression of a mutant form of the ferritin light chain gene induces neurodegeneration and iron overload in transgenic mice
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726993
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29 September 2017
Role of iron in neurodegenerative disorders
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PubMed Central
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29 September 2017
Huntingtin inclusion bodies are iron-dependent centers of oxidative events.
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PubMed Central
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29 September 2017
A century-old debate on protein aggregation and neurodegeneration enters the clinic
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726993
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29 September 2017
Neuroferritinopathy: missense mutation in FTL causing early-onset bilateral pallidal involvement.
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29 September 2017
Iron, brain ageing and neurodegenerative disorders
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29 September 2017
Neurodegeneration caused by proteins with an aberrant carboxyl-terminus
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PubMed Central
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29 September 2017
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726993
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29 September 2017
Late onset familial dystonia: could mitochondrial deficits induce a diffuse lesioning process of the whole basal ganglia system?
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726993
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29 September 2017
Iron-catalyzed hydroxyl radical formation. Stringent requirement for free iron coordination site
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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=3726993
retrieved
29 September 2017
Evidence that a salt bridge in the light chain contributes to the physical stability difference between heavy and light human ferritins.
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726993
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29 September 2017
Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498-499InsTC).
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726993
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4 September 2018
A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: description of clinical features and implications for genotype-phenotype correlations.
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PubMed Central
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4 September 2018
Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726993
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4 September 2018
Neuroferritinopathy in a Japanese family with a duplication in the ferritin light chain gene
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3726993
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4 September 2018
Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation.
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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=3726993
retrieved
4 September 2018
Hereditary ferritinopathy: a novel mutation, its cellular pathology, and pathogenetic insights.
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=3726993
retrieved
4 September 2018
Ferritinopathy: diagnosis by muscle or nerve biopsy, with a note on other nuclear inclusion body diseases.
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=3726993
retrieved
4 September 2018
Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide gene
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=3726993
retrieved
4 September 2018
Production and characterization of recombinant heteropolymers of human ferritin H and L chains
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/23908629
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.3389/FNAGI.2013.00032
1 reference
stated in
Europe PubMed Central
PMCID
3726993
retrieved
18 August 2017
PMCID
3726993
1 reference
stated in
Europe PubMed Central
PMCID
3726993
retrieved
18 August 2017
PubMed ID
23908629
1 reference
stated in
Europe PubMed Central
PMCID
3726993
retrieved
18 August 2017
ResearchGate publication ID
254282784
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