(Q37127064)

18 August 2017

Pathological relationships involving iron and myelin may constitute a shared mechanism linking various rare and common brain diseases (English)

1 reference

18 August 2017

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27500074%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

Conceicao Bettencourt

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27500074%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

John K. Olynyk

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27500074%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

11

Mina Ryten

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27500074%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

author name string

Moones Heidari

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27500074%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

Sam H Gerami

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27500074%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

Brianna Bassett

3

1 reference

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12 June 2020

Ross M Graham

4

1 reference

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12 June 2020

Anita C G Chua

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27500074%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

Ritambhara Aryal

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27500074%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

Michael J House

7

1 reference

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12 June 2020

Henry Houlden

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27500074%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

UK Brain Expression Consortium (UKBEC)

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27500074%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

Debbie Trinder

14

1 reference

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12 June 2020

Daniel M Johnstone

15

1 reference

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12 June 2020

Elizabeth A Milward

16

1 reference

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12 June 2020

publication date

22 June 2016

1 reference

Rare diseases (Austin, Tex.)

18 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27500074%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

volume

4

1 reference

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12 June 2020

issue

1

1 reference

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12 June 2020

page(s)

e1198458

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27500074%20AND%20SRC:MED&resulttype=core&format=json

Brain iron accumulation affects myelin-related molecular systems implicated in a rare neurogenetic disease family with neuropsychiatric features

12 June 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Gene co-expression networks shed light into diseases of brain iron accumulation

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Klotho Protects Dopaminergic Neuron Oxidant-Induced Degeneration by Modulating ASK1 and p38 MAPK Signaling Pathways

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

LINGO-1 antibody ameliorates myelin impairment and spatial memory deficits in experimental autoimmune encephalomyelitis mice

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

The neuroprotective effect of Klotho is mediated via regulation of members of the redox system

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Pantothenate kinase-associated neurodegeneration is not a synucleinopathy

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Klotho interferes with a novel FGF-signalling pathway and insulin/Igf-like signalling to improve longevity and stress resistance in Caenorhabditis elegans

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Molecular genetic approaches to understanding the roles and regulation of iron in brain health and disease

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

The KCl cotransporter isoform KCC3 can play an important role in cell growth regulation

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Proteolipid protein gene: Pelizaeus-Merzbacher disease in humans and neurodegeneration in mice

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Mutation of the mouse klotho gene leads to a syndrome resembling ageing

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Cp/Heph mutant mice have iron-induced neurodegeneration diminished by deferiprone.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Disruption of hemochromatosis protein and transferrin receptor 2 causes iron-induced liver injury in mice.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Novel mutation of the WDR45 gene causing beta-propeller protein-associated neurodegeneration.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Brain transcriptome perturbations in the transferrin receptor 2 mutant mouse support the case for brain changes in iron loading disorders, including effects relating to long-term depression and long-term potentiation.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Brain transcriptome perturbations in the Hfe(-/-) mouse model of genetic iron loading.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Iron efflux from oligodendrocytes is differentially regulated in gray and white matter.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Neuromuscular manifestations in hereditary haemochromatosis

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Genome-wide microarray analysis of brain gene expression in mice on a short-term high iron diet

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Premature aging-like phenotype in fibroblast growth factor 23 null mice is a vitamin D-mediated process

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

High cholesterol level is essential for myelin membrane growth

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4961263

Arena syndrome is caused by a missense mutation in PLP1

3 September 2018

1 reference

12 December 2020

Phenotypic heterogeneity in Woodhouse-Sakati syndrome: two new families with a mutation in the C2orf37 gene

1 reference

12 December 2020

Early manifestations of BPAN in a pediatric patient

1 reference

12 December 2020

Evaluation of Different Normalization and Analysis Procedures for Illumina Gene Expression Microarray Data Involving Small Changes.

1 reference

12 December 2020

10.1080/21675511.2016.1198458

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27500074%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27500074%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

PubMed publication ID

27500074

1 reference