(Q34579454)

English

Iron loading-induced aggregation and reduction of iron incorporation in heteropolymeric ferritin containing a mutant light chain that causes neurodegeneration

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Iron loading-induced aggregation and reduction of iron incorporation in heteropolymeric ferritin containing a mutant light chain that causes neurodegeneration (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

neurodegeneration

1 reference

based on heuristic

inferred from title

author name string

Barry B Muhoberac

1

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Martin A Baraibar

2

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Ruben Vidal

3

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

language of work or name

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publication date

26 October 2010

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

number of pages

5

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Biochimica et Biophysica Acta

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

1812

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

544-548

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

Accumulation of oxidative DNA damage in brain mitochondria in mouse model of hereditary ferritinopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040265

7 July 2018

Unraveling of the E-helices and disruption of 4-fold pores are associated with iron mishandling in a mutant ferritin causing neurodegeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040265

7 July 2018

Abnormal iron metabolism and oxidative stress in mice expressing a mutant form of the ferritin light polypeptide gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040265

7 July 2018

Iron-mediated aggregation and a localized structural change characterize ferritin from a mutant light chain polypeptide that causes neurodegeneration.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040265

7 July 2018

Expression of a mutant form of the ferritin light chain gene induces neurodegeneration and iron overload in transgenic mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040265

7 July 2018

Iron, brain ageing and neurodegenerative disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040265

7 July 2018

Neurodegeneration caused by proteins with an aberrant carboxyl-terminus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040265

7 July 2018

Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040265

7 July 2018

Comparison of the three-dimensional structures of recombinant human H and horse L ferritins at high resolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040265

7 July 2018

Evidence that a salt bridge in the light chain contributes to the physical stability difference between heavy and light human ferritins.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040265

7 July 2018

A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: description of clinical features and implications for genotype-phenotype correlations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040265

27 October 2018

Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040265

27 October 2018

Neuroferritinopathy in a Japanese family with a duplication in the ferritin light chain gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040265

27 October 2018

Hereditary ferritinopathy: a novel mutation, its cellular pathology, and pathogenetic insights

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040265

27 October 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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3040265

27 October 2018

The Role of the L-Chain in Ferritin Iron Incorporation

1 reference

https://pubmed.ncbi.nlm.nih.gov/21029774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thermal stability of horse spleen apoferritin and human recombinant H apoferritin

1 reference

https://pubmed.ncbi.nlm.nih.gov/21029774

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.BBADIS.2010.10.010

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 August 2017

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