Investigation of the role of mitochondrial DNA in multiple sclerosis susceptibility (Q33358078)

26 July 2017

title

Investigation of the role of mitochondrial DNA in multiple sclerosis susceptibility (English)

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26 July 2017

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Alastair Compston

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26 July 2017

Patrick Chinnery

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26 July 2017

Maria Ban

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26 July 2017

Joanna Elson

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26 July 2017

Amie Walton

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26 July 2017

Douglas Turnbull

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26 July 2017

Stephen Sawcer

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26 July 2017

language of work or name

English

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publication date

6 August 2008

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26 July 2017

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26 July 2017

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26 July 2017

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26 July 2017

page(s)

e2891

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Creative Commons Attribution 4.0 International

26 July 2017

start time

6 August 2008

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April 2022 Public Data File from Crossref

copyrighted

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cites work

Novel role for mitochondria: protein kinase Ctheta-dependent oxidative signaling organelles in activation-induced T-cell death

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494944

PEDSTATS: descriptive statistics, graphics and quality assessment for gene mapping data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494944

Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiency

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494944

The determination of complete human mitochondrial DNA sequences in single cells: implications for the study of somatic mitochondrial DNA point mutations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494944

Tracing European founder lineages in the Near Eastern mtDNA pool

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494944

Geographic patterns of mtDNA diversity in Europe

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494944

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494944

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494944

Classification of European mtDNAs from an analysis of three European populations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494944

Mitochondrial complex I deficiency leads to increased production of superoxide radicals and induction of superoxide dismutase

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494944

Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494944

New diagnostic criteria for multiple sclerosis: guidelines for research protocols

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494944

Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494944

Mitochondrial dysfunction as a cause of axonal degeneration in multiple sclerosis patients

21 June 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002891

Parent-of-origin effect in multiple sclerosis: observations in half-siblings

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002891

Sequence of mitochondrial DNA in patients with multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002891

Mitochondrial DNA variants in Bulgarian patients affected by multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002891

Population screening for association of mitochondrial haplogroups BM, J, K and M with multiple sclerosis: interrelation between haplogroup J and MS in Persian patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002891

Pedigree disequilibrium tests for multilocus haplotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002891

The power to detect disease associations with mitochondrial DNA haplogroups

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002891

Oxidative damage to DNA in plaques of MS brains

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2494944

Mitochondrial Protein Nitration Primes Neurodegeneration in Experimental Autoimmune Encephalomyelitis

31 October 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0002891

Oxidative damage to mitochondrial DNA and activity of mitochondrial enzymes in chronic active lesions of multiple sclerosis

21 January 2018

1 reference

12 December 2020

Mitochondrial haplogroups in Basque multiple sclerosis patients

1 reference

12 December 2020

Biochemical alterations in multiple sclerosis lesions and normal-appearing white matter detected by in vivo 31P and 1H spectroscopic imaging

1 reference

12 December 2020

No association of the 11778 mitochondrial DNA mutation and multiple sclerosis in Japan

1 reference

12 December 2020

Sequence of the human homologue of a mitochondrially encoded murine transplantation antigen in patients with multiple sclerosis

1 reference

12 December 2020

Characterization of the mitochondrial DNA in patients with multiple sclerosis

1 reference

12 December 2020

Mitochondrial DNA mutations in multiple sclerosis patients with severe optic involvement

1 reference

12 December 2020

Screening for Leber's hereditary optic neuropathy associated mitochondrial DNA mutations in patients with prominent optic neuritis

1 reference

12 December 2020

Mitochondrial DNA mutations in multiple sclerosis

1 reference

12 December 2020

Large scale screening of the mitochondrial DNA reveals no pathogenic mutations but a haplotype associated with multiple sclerosis in Caucasians

1 reference

12 December 2020

Characterization of the mitochondrial genome in childhood multiple sclerosis. II. Multiple sclerosis without optic neuritis and LHON-associated genes

1 reference

12 December 2020

Genetic variants of Complex I in multiple sclerosis

1 reference

12 December 2020

Mitochondrial dysfunction plays a key role in progressive axonal loss in Multiple Sclerosis

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0002891

Identifiers

DOI

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26 July 2017

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26 July 2017

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