Mitochondrial mutations are associated with atherosclerotic lesions in the human aorta

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Mitochondrial mutations are associated with atherosclerotic lesions in the human aorta is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1155/2012/832464
P932PMC publication ID3446814
P698PubMed publication ID22997526
P5875ResearchGate publication ID230895893

P50authorYuri V BobryshevQ88065781
Igor A. SobeninQ38323510
Alexander OrekhovQ51464003
Margarita SazonovaQ57081240
Anton PostnovQ59705092
P2860cites workMitochondrial DNA mutations in focal segmental glomerulosclerosis lesionsQ74381345
Detection of mitochondrial DNA mutations by temporal temperature gradient gel electrophoresisQ78077754
Studies of the human aortic intima by a direct quantitative assay of mutant alleles in the mitochondrial genomeQ82266504
The epidemiology of Leber hereditary optic neuropathy in the North East of EnglandQ24611047
Atherosclerosis — An Inflammatory DiseaseQ26776972
Metabolic consequences of a novel missense mutation of the mtDNA CO I geneQ28118499
Histochemical and molecular genetic study of MELAS and MERRF in Korean patientsQ31039066
Mutations of mitochondrial 12S rRNA in gastric carcinoma and their significanceQ33210189
Genetic instability and atherosclerosis: can somatic mutations account for the development of cardiovascular diseases?Q33947340
Determination of single-nucleotide polymorphisms by real-time pyrophosphate DNA sequencingQ35028450
Site-specific somatic mitochondrial DNA point mutations in patients with thymidine phosphorylase deficiencyQ35095598
The autoimmune concept of atherosclerosisQ35550211
Autoimmune and inflammatory mechanisms in atherosclerosisQ35698466
Comparison of GenFlex Tag Array and Pyrosequencing in SNP GenotypingQ35870298
Mitochondrial dysfunction and mitochondrial DNA mutations in atherosclerotic complications in diabetesQ35999426
Autoimmunity in atherosclerosis: a protective response losing control?Q37138017
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Atherosclerosis--an immune disease: The Anitschkov Lecture 2007.Q37308326
Rapid detection and estimation by pyrosequencing of 23S rRNA genes with a single nucleotide polymorphism conferring linezolid resistance in EnterococciQ40130643
The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency.Q43074243
Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III geneQ43074976
Antiatherogenic mitochondrial genotype in patients with type 2 diabetesQ43566537
Late onset of stroke-like episode associated with a 3256C-->T point mutation of mitochondrial DNA.Q44583856
A novel mitochondrial mutation, 1556C --> T, in a Japanese patient with streptomycin-induced tinnitusQ44894844
Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 geneQ48183315
A novel heteroplasmic tRNAleu(CUN) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapy.Q50512793
Variable clinical manifestation of homoplasmic G14459A mitochondrial DNA mutation.Q53770563
Catalytic activities of mitochondrial ATP synthase in patients with mitochondrial DNA T8993G mutation in the ATPase 6 gene encoding subunit aQ57010910
Autoantibody against oxidised LDL and progression of carotid atherosclerosisQ59704366
Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNAQ73031929
P275copyright licenseCreative Commons Attribution 3.0 UnportedQ14947546
P6216copyright statuscopyrightedQ50423863
P921main subjectaortaQ101004
atherosclerosisQ12252367
P304page(s)832464
P577publication date2012-09-11
P1433published inClinical and Developmental ImmunologyQ15754140
P1476titleMitochondrial mutations are associated with atherosclerotic lesions in the human aorta
P478volume2012

Reverse relations

cites work (P2860)
Q86885855Analysis of mitochondrial DNA heteroplasmic mutations A1555G, C3256T, T3336C, С5178А, G12315A, G13513A, G14459A, G14846А and G15059A in CHD patients with the history of myocardial infarction
Q36997420Association of mitochondrial genetic variation with carotid atherosclerosis
Q53276957Association of mitochondrial mutations with the age of patients having atherosclerotic lesions.
Q36872528Association of the level of heteroplasmy of the 15059G>A mutation in the MT-CYB mitochondrial gene with essential hypertension.
Q92703463Changes in Mitochondrial Genome Associated with Predisposition to Atherosclerosis and Related Disease
Q55419759Data on association of mitochondrial heteroplasmy and cardiovascular risk factors: Comparison of samples from Russian and Mexican populations.
Q34239967Emerging roles of mitochondria ROS in atherosclerotic lesions: causation or association?
Q89994270Heteroplasmic Variants of Mitochondrial DNA in Atherosclerotic Lesions of Human Aortic Intima
Q33600464Mitochondria, endothelial cell function, and vascular diseases
Q90883733Mitochondrial 3243A > G mutation confers pro-atherogenic and pro-inflammatory properties in MELAS iPS derived endothelial cells
Q48620870Mitochondrial DNA haplogroup D4b is a protective factor for ischemic stroke in Chinese Han population
Q46755952Mitochondrial multiorgan disorder syndrome score generated from definite mitochondrial disorders
Q35193558Mosaicism of mitochondrial genetic variation in atherosclerotic lesions of the human aorta.
Q41213847Quantitative assessment of heteroplasmy of mitochondrial genome: perspectives in diagnostics and methodological pitfalls
Q58792826Response to: Comment on "Role of Mitochondrial Genome Mutations in Pathogenesis of Carotid Atherosclerosis"

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