| scholarly article | Q13442814 |
| P2093 | author name string | Mohammad Mehdi Heidari | |
| Fatemeh Sedighi | |||
| Mahboobe Derakhshani | |||
| Seyed Khalil Foruzan-Nia | |||
| P2860 | cites work | Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups | Q24563892 |
| Rapid evolution of animal mitochondrial DNA | Q24597162 | ||
| Indian Siddis: African descendants with Indian admixture | Q24633482 | ||
| Sequence and organization of the human mitochondrial genome | Q27860659 | ||
| Distinctive features of the 5'-terminal sequences of the human mitochondrial mRNAs | Q28280119 | ||
| Mortality by cause for eight regions of the world: Global Burden of Disease Study | Q29615121 | ||
| Nucleotide substitution rate of mammalian mitochondrial genomes | Q33855171 | ||
| Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot? | Q33910255 | ||
| Promoting global cardiovascular health: moving forward | Q34179277 | ||
| The case for the continuing use of the revised Cambridge Reference Sequence (rCRS) and the standardization of notation in human mitochondrial DNA studies | Q34389694 | ||
| Mutation C3256T of mitochondrial genome in white blood cells: novel genetic marker of atherosclerosis and coronary heart disease. | Q34441663 | ||
| MITOMAP: a human mitochondrial genome database--1998 update | Q34649422 | ||
| Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegia | Q35059711 | ||
| The autoimmune concept of atherosclerosis | Q35550211 | ||
| Autoimmune and inflammatory mechanisms in atherosclerosis | Q35698466 | ||
| Mitochondrial dysfunction and mitochondrial DNA mutations in atherosclerotic complications in diabetes | Q35999426 | ||
| Autoimmunity in atherosclerosis: a protective response losing control? | Q37138017 | ||
| Mitochondrial DNA variant interactions modify breast cancer risk | Q37399988 | ||
| Novel Point Mutations in Frataxin Gene in Iranian Patients with Friedreich's Ataxia | Q37618449 | ||
| Mitochondrial DNA mutations in patients with postlingual, nonsyndromic hearing impairment | Q43784130 | ||
| Changes of mitochondria in atherosclerosis: possible determinant in the pathogenesis of the disease. | Q46167492 | ||
| A novel mitochondrial transfer RNA(Asn) mutation causing multiorgan failure. | Q50476705 | ||
| Kuopio Atherosclerosis Prevention Study (KAPS). A population-based primary preventive trial of the effect of LDL lowering on atherosclerotic progression in carotid and femoral arteries. | Q50595888 | ||
| Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations and mitochondrial deletions in Iranian patients with Friedreich's ataxia. | Q51236007 | ||
| Rapid concerted evolution in animal mitochondrial DNA. | Q51709065 | ||
| Deletions of muscle mitochondrial DNA | Q69920037 | ||
| Increased risk of stroke in patients with the A12308G polymorphism in mitochondria | Q73365367 | ||
| Role of mitochondrial DNA variants and copy number in diabetic atherogenesis | Q85226193 | ||
| P433 | issue | 10 | |
| P921 | main subject | atherosclerosis | Q12252367 |
| P304 | page(s) | 1379-1385 | |
| P577 | publication date | 2017-10-01 | |
| P1433 | published in | Iranian Journal of Public Health | Q15817212 |
| P1476 | title | Mutation Analysis of the Mitochondrial tRNA Genes in Iranian Coronary Atherosclerosis Patients | |
| P478 | volume | 46 |
| Q89521384 | Data on association of mitochondrial heteroplasmy with carotid intima-media thickness in subjects from Russian and Kazakh populations | cites work | P2860 |
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