| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1989PNAS...86.7952S |
| P356 | DOI | 10.1073/PNAS.86.20.7952 |
| P932 | PMC publication ID | 298190 |
| P698 | PubMed publication ID | 2554297 |
| P5875 | ResearchGate publication ID | 20602450 |
| P2093 | author name string | D C Wallace | |
| J M Shoffner | |||
| M T Lott | |||
| D A Costigan | |||
| A S Voljavec | |||
| S A Soueidan | |||
| P2860 | cites work | Clinical and biochemical correlations in mitochondrial myopathies treated with coenzyme Q10 | Q68352956 |
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| Heteroplasmy in mice with deletion of a large coding region of mitochondrial DNA | Q69823781 | ||
| Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy | Q69835096 | ||
| Deletions of muscle mitochondrial DNA | Q69920037 | ||
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| Sequence and organization of the human mitochondrial genome | Q27860659 | ||
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| Mitochondrial DNA deletion in Pearson's marrow/pancreas syndrome | Q28256452 | ||
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| Improvement of abnormal pyruvate metabolism and cardiac conduction defect with coenzyme Q10 in Kearns-Sayre syndrome | Q28307882 | ||
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| Complete sequence of bovine mitochondrial DNA. Conserved features of the mammalian mitochondrial genome | Q29618228 | ||
| Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration | Q33629847 | ||
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| Characterization of mitochondrial DNA in chloramphenicol-resistant interspecific hybrids and a cybrid | Q41549650 | ||
| Antioxidative effect of ubiquinones on mitochondrial membranes | Q41935786 | ||
| A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA. | Q41951578 | ||
| Deletion of blood mitochondrial DNA in pancytopenia | Q44936313 | ||
| The complete nucleotide sequence of the Xenopus laevis mitochondrial genome | Q48376185 | ||
| The frequency of matching sequences in DNA. | Q52693505 | ||
| Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies | Q59055292 | ||
| Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease | Q67950234 | ||
| P433 | issue | 20 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | mitochondrial DNA | Q27075 |
| P304 | page(s) | 7952-7956 | |
| P577 | publication date | 1989-10-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy | |
| P478 | volume | 86 |
| Q71548345 | 3.1-kb deletion of mitochondrial DNA in a patient with Kearns-Sayre syndrome |
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| Q28115983 | A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria |
| Q39732453 | A microfluidic system for fast detection of mitochondrial DNA deletion |
| Q24670009 | A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I |
| Q42558198 | A multipartite mitochondrial genome in the potato cyst nematode Globodera pallida. |
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| Q43182794 | A novel large-scale deletion of the mitochondrial DNA of spermatozoa of men in north iran. |
| Q37147048 | A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues |
| Q70765918 | A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathies |
| Q72391045 | A topoisomerase II cleavage site is associated with a novel mitochondrial DNA deletion |
| Q33918608 | A unique junctional palindromic sequence in mitochondrial DNA from a patient with progressive external ophthalmoplegia |
| Q40530947 | Accumulation of the common mitochondrial DNA deletion induced by ionizing radiation |
| Q41428595 | Age-associated alterations of the mitochondrial genome |
| Q41790765 | Age-related human mtDNA deletions: a heterogeneous set of deletions arising at a single pair of directly repeated sequences |
| Q72798686 | Ageing-associated tandem duplications in the D-loop of mitochondrial DNA of human muscle |
| Q77922003 | An alcoholic binge causes massive degradation of hepatic mitochondrial DNA in mice |
| Q24676151 | An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p |
| Q34586803 | Analysis of repeat-mediated deletions in the mitochondrial genome of Saccharomyces cerevisiae |
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| Q38354348 | Effects of Xenopus laevis mitochondrial single-stranded DNA-binding protein on primer-template binding and 3'-->5' exonuclease activity of DNA polymerase gamma |
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| Q34187826 | Human mitochondrial genetics |
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| Q71887424 | Investigation on the mitochondrial transfer RNA(Leu)(UUR) in blood cells from patients with cluster headache |
| Q51760977 | Is There Still Any Role for Oxidative Stress in Mitochondrial DNA-Dependent Aging? |
| Q24791429 | Is cumulative frequency of mitochondrial DNA variants a biomarker for colorectal tumor progression? |
| Q33672801 | Juvenile Kearns-Sayre syndrome initially misdiagnosed as a psychosomatic disorder |
| Q71853045 | Leber's hereditary optic neuropathy among Japanese |
| Q34793943 | Length heteroplasmies in human mitochondrial DNA control regions and breast cancer risk. |
| Q54918239 | Linear mitochondrial DNA is rapidly degraded by components of the replication machinery. |
| Q34427479 | Linear mtDNA fragments and unusual mtDNA rearrangements associated with pathological deficiency of MGME1 exonuclease |
| Q34733032 | Maintenance of human rearranged mitochondrial DNAs in long-term cultured transmitochondrial cell lines |
| Q33642751 | Management of hereditary retinal degenerations: present status and future directions |
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| Q67823092 | Mitochondria and aging: The universality of bioenergetic disease |
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| Q58136336 | Mitochondrial DNA and Disease |
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| Q27005350 | Mitochondrial DNA disease-molecular insights and potential routes to a cure |
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