Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.
about
Replication-competent human mitochondrial DNA lacking the heavy-strand promoter regionThe ophthalmologic manifestations of mitochondrial disease.Human mitochondrial genetics.DNA sequences proximal to human mitochondrial DNA deletion breakpoints prevalent in human disease form G-quadruplexes, a class of DNA structures inefficiently unwound by the mitochondrial replicative Twinkle helicase.Mitochondrial DNA 4977bp deletion mutation in peripheral blood reflects atrial remodeling in patients with non-valvular atrial fibrillation.Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant diseaseDefects of mitochondrial DNA.Disorders associated with multiple deletions of mitochondrial DNA.Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegiaDetection of a specific mitochondrial DNA deletion in tissues of older humans.Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA.Mutations in mitochondrial tRNA genes: a frequent cause of neuromuscular diseases.The NCS3 mutation: genetic evidence for the expression of ribosomal protein genes in Zea mays mitochondria.Disease progression in patients with single, large-scale mitochondrial DNA deletions.The generation of mitochondrial DNA large-scale deletions in human cells.Mitochondrial DNA rearrangements in health and disease--a comprehensive study.Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathies.Genomic evolution drives the evolution of the translation system.Mitochondrial DNA deletions inhibit proteasomal activity and stimulate an autophagic transcript.Allelic mutations of the fourth subunit of NADH dehydrogenase are not pathogenetically important in 11778-negative Leber hereditary optic neuropathy.Mitochondrial ND-I mutation in Leber hereditary optic neuropathy.Phylogenetic analysis of mitochondrial DNA in a patient with Kearns-Sayre syndrome containing a novel 7629-bp deletion.Friedreich's ataxia associated with mitochondrial myopathy: clinicopathologic report.Depletion of mitochondrial DNA and enzyme in estrogen-induced hamster kidney tumors: a rodent model of hormonal carcinogenesis.Potential relationship between the biological effects of low-dose irradiation and mitochondrial ROS production.
P2860
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P2860
Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.
description
1989 nî lūn-bûn
@nan
1989 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1989 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
name
Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.
@ast
Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.
@en
Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.
@nl
type
label
Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.
@ast
Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.
@en
Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.
@nl
prefLabel
Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.
@ast
Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.
@en
Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.
@nl
P2093
P2860
P356
P1476
Directly repeated sequences associated with pathogenic mitochondrial DNA deletions.
@en
P2093
P2860
P304
P356
10.1073/PNAS.86.20.8059
P407
P577
1989-10-01T00:00:00Z