(Q35023593)

5 August 2017

Systemic and cerebral iron homeostasis in ferritin knock-out mice (English)

1 reference

5 August 2017

Natalia VanDuyn

6

0 references

Bernardino F. Ghetti

12

object named as

Bernardino Ghetti

1 reference

5 August 2017

Wei Li

1

1 reference

5 August 2017

Holly J Garringer

2

1 reference

5 August 2017

Charles B Goodwin

3

1 reference

5 August 2017

Briana Richine

4

1 reference

5 August 2017

Anthony Acton

5

1 reference

5 August 2017

Barry B Muhoberac

7

1 reference

5 August 2017

Jose Irimia-Dominguez

8

1 reference

5 August 2017

Rebecca J Chan

9

1 reference

5 August 2017

Munro Peacock

10

1 reference

5 August 2017

Richard Nass

11

1 reference

5 August 2017

Ruben Vidal

13

1 reference

5 August 2017

language of work or name

English

0 references

publication date

28 January 2015

1 reference

5 August 2017

1 reference

5 August 2017

10

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5 August 2017

1

1 reference

5 August 2017

e0117435

1 reference

Creative Commons Attribution 4.0 International

5 August 2017

start time

28 January 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4309591/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

The physiological functions of iron regulatory proteins in iron homeostasis - an update

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

Iron-dependent regulation of hepcidin in Hjv-/- mice: evidence that hemojuvelin is dispensable for sensing body iron levels

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

Human L-ferritin deficiency is characterized by idiopathic generalized seizures and atypical restless leg syndrome.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

Abnormal iron homeostasis and neurodegeneration

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

Iron metabolism in the CNS: implications for neurodegenerative diseases

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

Noncoding variation of the gene for ferritin light chain in hereditary and age-related cataract

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

The metal transporter SMF-3/DMT-1 mediates aluminum-induced dopamine neuron degeneration

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

A mutant light-chain ferritin that causes neurodegeneration has enhanced propensity toward oxidative damage.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

Copper and iron disorders of the brain

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

Role of iron in neurodegenerative disorders

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

Neurodegeneration caused by proteins with an aberrant carboxyl-terminus

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

A mutation, in the iron-responsive element of H ferritin mRNA, causing autosomal dominant iron overload

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

Plasma ferritin determination as a diagnostic tool

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

Early embryonic lethality of H ferritin gene deletion in mice.

8 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0117435

Mouse brains deficient in H-ferritin have normal iron concentration but a protein profile of iron deficiency and increased evidence of oxidative stress.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0117435

Ceruloplasmin regulates iron levels in the CNS and prevents free radical injury.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4309591

H ferritin knockout mice: a model of hyperferritinemia in the absence of iron overload

25 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25629408

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Hereditary hyperferritinaemia cataract syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25629408

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0117435

1 reference

5 August 2017

0 references

1 reference

5 August 2017

1 reference