| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/HUMU.20378 |
| P8608 | Fatcat ID | release_wxza47hz6bb6ncudlafh2scngq |
| P698 | PubMed publication ID | 16947981 |
| P2093 | author name string | Douglas C Wallace | |
| Eduardo Ruiz-Pesini | |||
| P2860 | cites work | Mitochondrial DNA and human evolution | Q22122407 |
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| Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family | Q30499211 | ||
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| Effects of purifying and adaptive selection on regional variation in human mtDNA. | Q39413917 | ||
| Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNAGln | Q43075276 | ||
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| Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation. | Q50476427 | ||
| Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity. | Q50527497 | ||
| Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients. | Q53206553 | ||
| Sequence variation in the tRNA genes of human mitochondrial DNA. | Q54358494 | ||
| Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation. | Q55404336 | ||
| Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease | Q67950234 | ||
| Point mutations in mitochondrial tRNA genes: sequence analysis of chronic progressive external ophthalmoplegia (CPEO) | Q71657315 | ||
| Novel mutation in the mitochondrial DNA tRNA glycine gene associated with sudden unexpected death | Q71719324 | ||
| Specific binding of aminoglycosides to a human rRNA construct based on a DNA polymorphism which causes aminoglycoside-induced deafness | Q73745096 | ||
| Paradoxes in longevity: sequence analysis of mtDNA haplogroup J in centenarians | Q74554779 | ||
| The myth and reality of reversal of aging by hormesis | Q82206156 | ||
| P433 | issue | 11 | |
| P921 | main subject | mitochondrial DNA | Q27075 |
| P304 | page(s) | 1072-1081 | |
| P577 | publication date | 2006-11-01 | |
| P1433 | published in | Human Mutation | Q5937269 |
| P1476 | title | Evidence for adaptive selection acting on the tRNA and rRNA genes of human mitochondrial DNA. | |
| P478 | volume | 27 |
| Q37377147 | A Comprehensive Characterization of Mitochondrial Genome in Papillary Thyroid Cancer |
| Q37073167 | A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function. |
| Q38044924 | A disproportionate role for mtDNA in Dobzhansky-Muller incompatibilities? |
| Q40146692 | A hypertension-associated mitochondrial DNA mutation alters the tertiary interaction and function of tRNALeu(UUR). |
| Q34211127 | A mitochondrial etiology of Alzheimer and Parkinson disease |
| Q34628968 | A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations |
| Q41878552 | Accumulation of slightly deleterious mutations in the mitochondrial genome: a hallmark of animal domestication |
| Q35608504 | An enhanced MITOMAP with a global mtDNA mutational phylogeny |
| Q55191330 | Analysis of mitochondrial A1555G mutation in infants with hearing impairment. |
| Q54312191 | Analysis of mitochondrial DNA sequence variants in patients with polycystic ovary syndrome. |
| Q21092461 | Ancient mtDNA genetic variants modulate mtDNA transcription and replication |
| Q46515103 | Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation. |
| Q35510313 | Bioenergetic origins of complexity and disease |
| Q37785510 | Bioenergetics and the epigenome: Interface between the environment and genes in common diseases |
| Q30645106 | Bioenergetics in human evolution and disease: implications for the origins of biological complexity and the missing genetic variation of common diseases |
| Q34851835 | Characterization of human GTPBP3, a GTP-binding protein involved in mitochondrial tRNA modification |
| Q31120276 | Clinical significance in oral cavity squamous cell carcinoma of pathogenic somatic mitochondrial mutations |
| Q53101980 | Comprehensive analysis of common and rare mitochondrial DNA variants in elite Japanese athletes: a case-control study. |
| Q22252552 | Correcting for purifying selection: an improved human mitochondrial molecular clock |
| Q41789320 | Detecting heteroplasmy from high-throughput sequencing of complete human mitochondrial DNA genomes |
| Q36594019 | Endothelial Cell Bioenergetics and Mitochondrial DNA Damage Differ in Humans Having African or West Eurasian Maternal Ancestry. |
| Q35632855 | Energetics, epigenetics, mitochondrial genetics |
| Q39141825 | Estimate of within population incremental selection through branch imbalance in lineage trees. |
| Q40012463 | Experimental assessment of bioenergetic differences caused by the common European mitochondrial DNA haplogroups H and T. |
| Q21142693 | Explaining the imperfection of the molecular clock of hominid mitochondria |
| Q53792022 | Fine Time Scaling of Purifying Selection on Human Nonsynonymous mtDNA Mutations Based on the Worldwide Population Tree and Mother-Child Pairs. |
| Q35008978 | Frequency and pattern of heteroplasmy in the complete human mitochondrial genome. |
| Q34531549 | Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics |
| Q36905252 | Functional recurrent mutations in the human mitochondrial phylogeny: dual roles in evolution and disease |
| Q99579694 | Genetic hitchhiking, mitonuclear coadaptation, and the origins of mt DNA barcode gaps |
| Q39396837 | Global DNA methylation levels are modulated by mitochondrial DNA variants |
| Q44375134 | Influence of mtDNA genetic variation on antibiotic therapy. |
| Q40062641 | Large scale mtDNA sequencing reveals sequence and functional conservation as major determinants of homoplasmic mtDNA variant distribution |
| Q45865052 | Leber Hereditary Optic Neuropathy: Exemplar of an mtDNA Disease |
| Q41915881 | MITOMASTER: a bioinformatics tool for the analysis of mitochondrial DNA sequences |
| Q50439126 | Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese family. |
| Q28393038 | Mechanisms of aminoglycoside ototoxicity and targets of hair cell protection |
| Q33320680 | Mitigating mutational meltdown in mammalian mitochondria |
| Q29616610 | Mitochondria and cancer |
| Q36724311 | Mitochondria as chi. |
| Q33517075 | Mitochondria, bioenergetics, and the epigenome in eukaryotic and human evolution |
| Q37806816 | Mitochondrial 12S rRNA mutations associated with aminoglycoside ototoxicity |
| Q33869557 | Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss |
| Q37258708 | Mitochondrial DNA genetics and the heteroplasmy conundrum in evolution and disease. |
| Q24642565 | Mitochondrial DNA haplogroups influence AIDS progression |
| Q55223565 | Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity. |
| Q55052993 | Mitochondrial DNA mutations in disease and aging. |
| Q37721270 | Mitochondrial DNA variation in human metabolic rate and energy expenditure |
| Q26781103 | Mitochondrial DNA variation in human radiation and disease |
| Q39230101 | Mitochondrial antibiograms in personalized medicine. |
| Q35632864 | Mitochondrial energetics and therapeutics |
| Q45925424 | Mitochondrial genetic background plays a role in increasing risk to asthma. |
| Q37455749 | Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation |
| Q47161404 | Mitochondrial mutations in 12S rRNA and 16S rRNA presenting as chronic progressive external ophthalmoplegia (CPEO) plus: A case report |
| Q50430537 | Mitochondrial ribosome and Ménière's disease: a pilot study. |
| Q46246554 | Mitochondrial tRNA glutamine variant in hypertrophic cardiomyopathy. |
| Q37648407 | Mitochondrial tRNA variants in Chinese subjects with coronary heart disease |
| Q92654743 | Mitochondrial tRNAAla 5601C>T variant may affect the clinical expression of the LHON‑related ND4 11778G>A mutation in a family |
| Q34367770 | Mitochondrial-nuclear epistasis: implications for human aging and longevity |
| Q27692574 | Mitonuclear interactions: evolutionary consequences over multiple biological scales |
| Q37150862 | MtDNA mutation pattern in tumors and human evolution are shaped by similar selective constraints. |
| Q33622660 | Multiplex analysis of mitochondrial DNA pathogenic and polymorphic sequence variants. |
| Q33339719 | Mutation patterns of mtDNA: empirical inferences for the coding region |
| Q33850305 | Mutations in mitochondrial tRNA genes may be related to insulin resistance in women with polycystic ovary syndrome |
| Q89530552 | Negative frequency dependent selection contributes to the maintenance of a global polymorphism in mitochondrial DNA |
| Q55643143 | Next-generation sequencing profiling of mitochondrial genomes in gout. |
| Q33373844 | Performance of mitochondrial DNA mutations detecting early stage cancer |
| Q47806814 | Predicting the pathogenicity of novel variants in mitochondrial tRNA with MitoTIP. |
| Q37395190 | Relaxation of selective constraints on avian mitochondrial DNA following the degeneration of flight ability |
| Q42950033 | Reply to letter from Felice L. Bedford and Doron Yacobi |
| Q90712112 | Screening for mitochondrial 12S rRNA C1494T mutation in 655 patients with non-syndromic hearing loss: An observational study |
| Q30362183 | Segregation of Naturally Occurring Mitochondrial DNA Variants in a Mini-Pig Model |
| Q36653669 | Severity of cardiomyopathy associated with adenine nucleotide translocator-1 deficiency correlates with mtDNA haplogroup |
| Q27333828 | Strong purifying selection in transmission of mammalian mitochondrial DNA |
| Q52663276 | The Mitochondrial tRNALeu(UUR) A3302G Mutation may be Associated With Insulin Resistance in Woman With Polycystic Ovary Syndrome. |
| Q42034984 | The diversity present in 5140 human mitochondrial genomes |
| Q37600061 | The novel mitochondrial 16S rRNA 2336T>C mutation is associated with hypertrophic cardiomyopathy |
| Q37287583 | The pathophysiology of mitochondrial disease as modeled in the mouse |
| Q37606811 | The role of mitochondria in health and disease |
| Q38100717 | The role of mitochondrial DNA mutations in hearing loss |
| Q37262055 | Variants in mitochondrial tRNA gene may not be associated with thyroid carcinoma |
| Q39256320 | Whole mitochondrial genome screening in two families with hearing loss: detection of a novel mutation in the 12S rRNA gene. |
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