| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2011PLoSO...616455M |
| P356 | DOI | 10.1371/JOURNAL.PONE.0016455 |
| P932 | PMC publication ID | 3027676 |
| P698 | PubMed publication ID | 21298061 |
| P5875 | ResearchGate publication ID | 49814331 |
| P50 | author | Barbara Kofler | Q37830634 |
| Johannes A Mayr | Q37843434 | ||
| Bernhard Iglseder | Q39186236 | ||
| P2093 | author name string | Wolfgang Patsch | |
| Wolfgang Sperl | |||
| Bernhard Paulweber | |||
| Edith E Mueller | |||
| Waltraud Eder | |||
| Raimund Weitgasser | |||
| Hannes Oberkofler | |||
| Richard Maier | |||
| Olaf Stanger | |||
| Franz Krempler | |||
| Sabine Ebner | |||
| Danijela Santic | |||
| Eva Schwaiger | |||
| Tanja Kreindl | |||
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| Association of the mitochondrial DNA 16189 T to C variant with lacunar cerebral infarction: evidence from a hospital-based case-control study | Q44883081 | ||
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| Increased oxidative damage with altered antioxidative status in type 2 diabetic patients harboring the 16189 T to C variant of mitochondrial DNA. | Q46555080 | ||
| Association of mitochondrial deoxyribonucleic acid 16189 variant (T->C transition) with metabolic syndrome in Chinese adults | Q46561790 | ||
| A common mitchondrial DNA variant is associated with thinness in mothers and their 20-yr-old offspring. | Q46584952 | ||
| Mitochondrial polymorphisms and susceptibility to type 2 diabetes-related traits in Finns | Q46687091 | ||
| A common mitochondrial DNA variant associated with susceptibility to dilated cardiomyopathy in two different populations | Q46732754 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | coronary artery disease | Q844935 |
| P304 | page(s) | e16455 | |
| P577 | publication date | 2011-01-26 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | The mitochondrial T16189C polymorphism is associated with coronary artery disease in Middle European populations | |
| P478 | volume | 6 |
| Q43500445 | Association of mitochondrial DNA displacement loop polymorphisms and aggressive periodontitis in a Chinese population: a pilot study |
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| Q90578301 | Atherosclerosis Can Be Mitochondrial: A Review |
| Q47133228 | Detection of somatic mutations in the mitochondrial DNA control region D-loop in brain tumors: The first report in Malaysian patients. |
| Q43454986 | Do mitochondria contribute to left ventricular non-compaction cardiomyopathy? New findings from myocardium of patients with left ventricular non-compaction cardiomyopathy |
| Q87107302 | Identification of sequence polymorphisms in the mitochondrial displacement loop as risk factors for sporadic and familial breast cancer |
| Q57175639 | Integrating Genes Affecting Coronary Artery Disease in Functional Networks by Multi-OMICs Approach |
| Q46600354 | Manganese-superoxide dismutase (Mn-SOD) overexpression is a common event in colorectal cancers with mitochondrial microsatellite instability |
| Q35760460 | Mitochondrial Haplogroup T Is Associated with Obesity in Austrian Juveniles and Adults |
| Q55341636 | Mitochondrial T16189C Polymorphism Is Associated with Metabolic Syndrome in the Mexican Population. |
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| Q37648407 | Mitochondrial tRNA variants in Chinese subjects with coronary heart disease |
| Q33659216 | Oxidative Stress Genes, Antioxidants and Coronary Artery Disease in Type 2 Diabetes Mellitus |
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| Q89747832 | The role of control region mitochondrial DNA mutations in cardiovascular disease: stroke and myocardial infarction |
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