| scholarly article | Q13442814 |
| P50 | author | Safia Messaoudi | Q83113219 |
| P2093 | author name string | Moiz Bakhiet | |
| Safa Taha | |||
| Ghada Al-Kafaji | |||
| Noureddine Ben Khalaf | |||
| Abdulqader Daif | |||
| Maram Atallah Alharbi | |||
| P2860 | cites work | Initial immunopathogenesis of multiple sclerosis: innate immune response. | Q38156767 |
| Structure and function of mitochondrial complex I. | Q38752775 | ||
| Mitochondria in neuroinflammation - Multiple sclerosis (MS), leber hereditary optic neuropathy (LHON) and LHON-MS. | Q39408815 | ||
| Risk factors for multiple sclerosis in Kuwait: a population-based case-control study | Q39534824 | ||
| Genetic and functional analysis of mitochondrial DNA-encoded complex I genes | Q40559250 | ||
| Lack of assembly of mitochondrial DNA-encoded subunits of respiratory NADH dehydrogenase and loss of enzyme activity in a human cell mutant lacking the mitochondrial ND4 gene product | Q40873588 | ||
| Detecting heteroplasmy from high-throughput sequencing of complete human mitochondrial DNA genomes | Q41789320 | ||
| Role of diffuse low-level heteroplasmy of mitochondrial DNA in Alzheimer's disease neurodegeneration | Q42103602 | ||
| Complex I deficiency in Persian multiple sclerosis patients | Q42169054 | ||
| Identification of deleterious synonymous variants in human genomes | Q42602176 | ||
| Age at onset of multiple sclerosis may be influenced by place of residence during childhood rather than ancestry | Q43476275 | ||
| Cell sorting experiments link persistent mitochondrial DNA damage with loss of mitochondrial membrane potential and apoptotic cell death | Q44211070 | ||
| Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis | Q44557768 | ||
| Mitochondrial complex I-linked disease | Q46591466 | ||
| Mitochondrial dysfunction as a cause of axonal degeneration in multiple sclerosis patients | Q47660422 | ||
| Novel mutations of ND genes in complex I deficiency associated with mitochondrial encephalopathy | Q48153107 | ||
| Comprehensive scanning of the entire mitochondrial genome for mutations. | Q53663390 | ||
| Mitochondrial complex I gene variations; as a potential genetic risk factor in pathogenesis of multiple sclerosis. | Q54193331 | ||
| Synonymous Mutations Frequently Act as Driver Mutations in Human Cancers | Q55554493 | ||
| '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 | ||
| Mitochondrial dysfunction in Parkinson's disease | Q60290965 | ||
| Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutations | Q64048994 | ||
| Peripheral blood mitochondrial DNA copy number as a novel potential biomarker for diabetic nephropathy in type 2 diabetes patients. | Q64984722 | ||
| Mitochondrial DNA diseases: Genotype and phenotype in leber's hereditary optic neuropathy | Q71853041 | ||
| Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population | Q73841466 | ||
| Oxidative damage to mitochondrial DNA and activity of mitochondrial enzymes in chronic active lesions of multiple sclerosis | Q74297187 | ||
| Targeting Mitochondrial Metabolism in Neuroinflammation: Towards a Therapy for Progressive Multiple Sclerosis | Q90905255 | ||
| Diagnostic criteria for multiple sclerosis: 2010 revisions to the McDonald criteria | Q24605493 | ||
| Mitochondrial DNA mutations in human disease | Q24676881 | ||
| Multiple sclerosis in the Arabian Gulf countries: a consensus statement | Q26851940 | ||
| Environmental risk factors for multiple sclerosis: a review with a focus on molecular mechanisms | Q27006548 | ||
| Artemis: sequence visualization and annotation | Q27861024 | ||
| The mtDNA-encoded ND6 subunit of mitochondrial NADH dehydrogenase is essential for the assembly of the membrane arm and the respiratory function of the enzyme | Q28368398 | ||
| SDM--a server for predicting effects of mutations on protein stability and malfunction | Q30402863 | ||
| mtDNA nt13708A variant increases the risk of multiple sclerosis | Q33319550 | ||
| The mitochondrial genome: structure, transcription, translation and replication | Q33540909 | ||
| Environmental factors and multiple sclerosis severity: a descriptive study. | Q33834066 | ||
| Towards the molecular mechanism of respiratory complex I. | Q34020648 | ||
| Review: Mitochondria and disease progression in multiple sclerosis | Q34308687 | ||
| Repair of oxidative DNA damage in nuclear and mitochondrial DNA, and some changes with aging in mammalian cells | Q34615837 | ||
| Genetics and pathogenesis of multiple sclerosis | Q35004746 | ||
| Mitochondrial threshold effects. | Q35017647 | ||
| Multiple sclerosis: pathogenesis and treatment | Q35151851 | ||
| The role of mitochondrial DNA mutation on neurodegenerative diseases | Q35152954 | ||
| Time-course effect of high-glucose-induced reactive oxygen species on mitochondrial biogenesis and function in human renal mesangial cells. | Q35739480 | ||
| Multiple sclerosis review. | Q35958691 | ||
| Multiple sclerosis--the plaque and its pathogenesis | Q36410882 | ||
| Mitochondrial respiratory complex I: structure, function and implication in human diseases | Q36444688 | ||
| Mitochondrial DNA mutations, energy metabolism and apoptosis in aging muscle | Q36463506 | ||
| Universal heteroplasmy of human mitochondrial DNA. | Q36477684 | ||
| The functional relevance of somatic synonymous mutations in melanoma and other cancers | Q36805023 | ||
| Association of common mitochondrial DNA variants with multiple sclerosis and systemic lupus erythematosus | Q36935909 | ||
| Sex and gender issues in multiple sclerosis | Q36999743 | ||
| Environmental factors and multiple sclerosis. | Q37085108 | ||
| Mitochondrial DNA genetics and the heteroplasmy conundrum in evolution and disease. | Q37258708 | ||
| Natural history of multiple sclerosis symptoms | Q37442391 | ||
| Is multiple sclerosis a mitochondrial disease? | Q37466077 | ||
| Latitude is significantly associated with the prevalence of multiple sclerosis: a meta-analysis | Q37863350 | ||
| P433 | issue | 6 | |
| P304 | page(s) | 257-268 | |
| P577 | publication date | 2019-11-04 | |
| P1433 | published in | Biomedical Reports | Q26853995 |
| P1476 | title | Four novel mutations in the mitochondrial ND4 gene of complex I in patients with multiple sclerosis | |
| P478 | volume | 11 |
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