scholarly article | Q13442814 |
P2093 | author name string | Zhang C | |
Baumer A | |||
Maxwell RJ | |||
Linnane AW | |||
Nagley P | |||
P2860 | cites work | Sequence and organization of the human mitochondrial genome | Q27860659 |
Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy | Q34312609 | ||
Detection of a specific mitochondrial DNA deletion in tissues of older humans | Q35891834 | ||
Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA. | Q35907687 | ||
Ageing-associated 5 kb deletion in human liver mitochondrial DNA. | Q41190023 | ||
Age-associated accumulation of 8-hydroxydeoxyguanosine in mitochondrial DNA of human diaphragm | Q41879903 | ||
Different copy numbers of apparently identically deleted mitochondrial DNA in tissues from a patient with Kearns-Sayre syndrome detected by PCR. | Q43514377 | ||
Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescence | Q44498466 | ||
Studies of sequence heterogeneity of mitochondrial DNA from rat and mouse tissues: evidence for an increased frequency of deletions/additions with aging. | Q52251595 | ||
An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region | Q57588514 | ||
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies | Q59055292 | ||
DECLINE IN SKELETAL MUSCLE MITOCHONDRIAL RESPIRATORY CHAIN FUNCTION: POSSIBLE FACTOR IN AGEING | Q61874684 | ||
Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy | Q68424891 | ||
Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases | Q69368213 | ||
Multiple deletions in mitochondrial DNA at direct repeats of non-D-loop regions in cases of familial mitochondrial myopathy | Q69392011 | ||
Age-dependent increase in deleted mitochondrial DNA in the human heart: possible contributory factor to presbycardia | Q70160150 | ||
P433 | issue | 1-2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | mitochondrial DNA | Q27075 |
P304 | page(s) | 34-38 | |
P577 | publication date | 1992-02-01 | |
P1433 | published in | FEBS Letters | Q1388051 |
P1476 | title | Multiple mitochondrial DNA deletions in an elderly human individual | |
P478 | volume | 297 |
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