| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2008PLoSO...3.1530Y |
| P356 | DOI | 10.1371/JOURNAL.PONE.0001530 |
| P932 | PMC publication ID | 2217590 |
| P698 | PubMed publication ID | 18270557 |
| P5875 | ResearchGate publication ID | 5580675 |
| P50 | author | Kjell-Morten Myhr | Q64539690 |
| Sverre J Mörk | Q117803414 | ||
| Janna Saarela | Q30501405 | ||
| Joerg T. Epplen | Q41713571 | ||
| Maria Giovanna Marrosu | Q42408301 | ||
| Saleh Ibrahim | Q43139623 | ||
| P2093 | author name string | Dirk Koczan | |
| Anna-Maija Sulonen | |||
| Manuel Comabella | |||
| Xavier Montalban | |||
| Denis A Akkad | |||
| Peter Rieckmann | |||
| Gianna Costa | |||
| Xinhua Yu | |||
| Antje Kroner | |||
| Daniela Corongiu | |||
| Hans-Juergen Thiesen | |||
| Harald I Nyland | |||
| Montserrat Camina-Tato | |||
| Robert Goertsches | |||
| P2860 | cites work | Parent-child concordance in multiple sclerosis | Q70174854 |
| Regional and temporal variation in the incidence of multiple sclerosis in Finland 1979-1993 | Q73473404 | ||
| Mitochondrial DNA mutations in multiple sclerosis | Q73822072 | ||
| mtDNA haplogroup J: a contributing factor of optic neuritis | Q77421708 | ||
| Is the mitochondrial DNA involved in determining susceptibility to multiple sclerosis? | Q77530983 | ||
| Large scale screening of the mitochondrial DNA reveals no pathogenic mutations but a haplotype associated with multiple sclerosis in Caucasians | Q77926568 | ||
| Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease | Q22337234 | ||
| Classification of European mtDNAs from an analysis of three European populations | Q24533221 | ||
| Disruption of the uncoupling protein-2 gene in mice reveals a role in immunity and reactive oxygen species production | Q28139177 | ||
| Mitochondrial DNA inherited variants are associated with successful aging and longevity in humans | Q28143058 | ||
| Mitochondrial DNA polymorphisms associated with longevity in a Finnish population | Q28217719 | ||
| Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy | Q28300484 | ||
| mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region | Q28762142 | ||
| Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease | Q29398392 | ||
| New diagnostic criteria for multiple sclerosis: guidelines for research protocols | Q34271601 | ||
| Mitochondrial defects in neurodegenerative disease | Q34366678 | ||
| Mitochondrial DNA and human evolution. | Q34560425 | ||
| Uncoupling protein 2 has protective function during experimental autoimmune encephalomyelitis. | Q35088315 | ||
| Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484. | Q35238441 | ||
| mtDNA mutations and common neurodegenerative disorders | Q36254228 | ||
| LEBER'S DISEASE WITH SYMPTOMS RESEMBLING DISSEMINATED SCLEROSIS | Q37119019 | ||
| Impairment of central and peripheral myelin in mitochondrial diseases | Q41378824 | ||
| The power to detect disease associations with mitochondrial DNA haplogroups | Q43259568 | ||
| Mitochondrial DNA variants in Bulgarian patients affected by multiple sclerosis | Q43928632 | ||
| Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis | Q44557768 | ||
| Mitochondrial polymorphisms and susceptibility to type 2 diabetes-related traits in Finns | Q46687091 | ||
| Analysis of Genetic Variation in the GenomEUtwin Project | Q47377818 | ||
| Population screening for association of mitochondrial haplogroups BM, J, K and M with multiple sclerosis: interrelation between haplogroup J and MS in Persian patients. | Q51312107 | ||
| Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients | Q53206553 | ||
| 'Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation | Q57009422 | ||
| Parent-of-origin effect in multiple sclerosis: observations in half-siblings | Q57317733 | ||
| Evidence from mtDNA sequences that common laboratory strains of inbred mice are descended from a single female | Q59071263 | ||
| Association of a common polymorphism in the promoter of UCP2 with susceptibility to multiple sclerosis | Q60689182 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | multiple sclerosis | Q8277 |
| P304 | page(s) | e1530 | |
| P577 | publication date | 2008-02-13 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | mtDNA nt13708A variant increases the risk of multiple sclerosis | |
| P478 | volume | 3 |
| Q47959866 | Association of UCP2 -866 G/A polymorphism with chronic inflammatory diseases |
| Q36311088 | Clinically proven mtDNA mutations are not common in those with chronic fatigue syndrome. |
| Q37034596 | Dissecting the effects of mtDNA variations on complex traits using mouse conplastic strains. |
| Q91672723 | Four novel mutations in the mitochondrial ND4 gene of complex I in patients with multiple sclerosis |
| Q46270458 | Generation and Bioenergetic Profiles of Cybrids with East Asian mtDNA Haplogroups |
| Q37466077 | Is multiple sclerosis a mitochondrial disease? |
| Q24600533 | May "mitochondrial eve" and mitochondrial haplogroups play a role in neurodegeneration and Alzheimer's disease? |
| Q51840198 | Mitochondrial DNA polymorphisms are associated with susceptibility and phenotype of systemic lupus erythematosus |
| Q28710285 | Mitochondrial DNA sequence variation and neurodegeneration |
| Q41844017 | Mitochondrial DNA sequence variation in multiple sclerosis. |
| Q91982232 | Mitochondrial Dysfunction and Multiple Sclerosis |
| Q46646521 | Mitochondrial gene polymorphism is associated with gut microbial communities in mice |
| Q38908404 | MtDNA T4216C variation in multiple sclerosis: a systematic review and meta-analysis |
| Q64098211 | MtDNA population variation in Myalgic encephalomyelitis/Chronic fatigue syndrome in two populations: a study of mildly deleterious variants |
| Q38106595 | Multiple sclerosis and mitochondrial gene variations: A review |
| Q33942825 | Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases |
| Q54274045 | Polymorphisms in the mitochondrially encoded ATP synthase 8 gene are associated with susceptibility to bullous pemphigoid in the German population. |
| Q34544496 | Principal-component analysis for assessment of population stratification in mitochondrial medical genetics |
| Q37862835 | Role of gender in multiple sclerosis: Clinical effects and potential molecular mechanisms |
| Q34390958 | Sex-specific regulation of mitochondrial DNA levels: genome-wide linkage analysis to identify quantitative trait loci |
| Q39161650 | Stressed cybrids model demyelinated axons in multiple sclerosis. |
| Q92454632 | The second genome: Effects of the mitochondrial genome on cancer progression |
| Q58122630 | mtDNA Population Variants and Neurodegenerative Diseases |
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