(Q44452930)

3 December 2017

title

Evidence for adaptive selection acting on the tRNA and rRNA genes of human mitochondrial DNA. (English)

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3 December 2017

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Eduardo Ruiz-Pesini

1

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3 December 2017

Douglas C Wallace

series ordinal

2

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3 December 2017

publication date

1 November 2006

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3 December 2017

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3 December 2017

volume

27

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3 December 2017

issue

11

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3 December 2017

page(s)

1072-1081

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20378

3 December 2017

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Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNAGln

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Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity.

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Specific binding of aminoglycosides to a human rRNA construct based on a DNA polymorphism which causes aminoglycoside-induced deafness

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Point mutations in mitochondrial tRNA genes: sequence analysis of chronic progressive external ophthalmoplegia (CPEO)

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Search for characteristic structural features of mammalian mitochondrial tRNAs.

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Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups

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A molecular basis for human hypersensitivity to aminoglycoside antibiotics

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A mitochondrial DNA clone is associated with increased risk for Alzheimer disease

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Mechanisms and convergence of compensatory evolution in mammalian mitochondrial tRNAs

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The role of selection in the evolution of human mitochondrial genomes

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Interaction of avilamycin with ribosomes and resistance caused by mutations in 23S rRNA.

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Prediction of pathogenic mutations in mitochondrially encoded human tRNAs

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Phylogeny of east Asian mitochondrial DNA lineages inferred from complete sequences

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Assigning pathogenicity to mitochondrial tRNA mutations: when "definitely maybe" is not good enough

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Natural selection shaped regional mtDNA variation in humans

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Differences of sperm motility in mitochondrial DNA haplogroup U sublineages

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cDNA sequence of a human skeletal muscle ADP/ATP translocator: lack of a leader peptide, divergence from a fibroblast translocator cDNA, and coevolution with mitochondrial DNA genes

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The human ATP synthase beta subunit gene: sequence analysis, chromosome assignment, and differential expression

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Phylogeny of mitochondrial DNA macrohaplogroup N in India, based on complete sequencing: implications for the peopling of South Asia

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Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

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Paradoxes in longevity: sequence analysis of mtDNA haplogroup J in centenarians

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Effects of purifying and adaptive selection on regional variation in human mtDNA.

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Novel mutation in the mitochondrial DNA tRNA glycine gene associated with sudden unexpected death

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Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

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Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.

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The myth and reality of reversal of aging by hormesis

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Secondary structure and patterns of evolution among mammalian mitochondrial 12S rRNA molecules

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Decreased CCA-addition in human mitochondrial tRNAs bearing a pathogenic A4317G or A10044G mutation.

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Sequence variation in the tRNA genes of human mitochondrial DNA.

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Sequence analysis of cDNAs for the human and bovine ATP synthase beta subunit: mitochondrial DNA genes sustain seventeen times more mutations

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Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease

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mtDNA variation, climatic adaptation, degenerative diseases, and longevity

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A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine

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Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation.

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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

1 reference

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7 January 2021

Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation.

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7 January 2021

Identifiers

DOI

10.1002/HUMU.20378

1 reference

release_wxza47hz6bb6ncudlafh2scngq

3 December 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/wxza47hz6bb6ncudlafh2scngq

24 November 2022

mapped directly with Wikidata item

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