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Mitochondrial tRNA mutations and disease
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PubMed
review article
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Europe PubMed Central
title
Mitochondrial tRNA mutations and disease
(English)
1 reference
stated in
PubMed
main subject
mitochondrion
1 reference
based on heuristic
inferred from title
author
Emma L. Blakely
series ordinal
3
object named as
Emma L. Blakely
1 reference
stated in
Crossref
Robert William Taylor
series ordinal
5
object named as
Robert W. Taylor
1 reference
stated in
Crossref
author name string
John W. Yarham
series ordinal
1
1 reference
stated in
Crossref
Joanna L. Elson
series ordinal
2
1 reference
stated in
Crossref
Robert McFarland
series ordinal
4
1 reference
stated in
Crossref
language of work or name
English
1 reference
stated in
PubMed
publication date
September 2010
1 reference
stated in
PubMed
published in
Wiley interdisciplinary reviews. RNA
1 reference
stated in
PubMed
volume
1
1 reference
stated in
PubMed
issue
2
1 reference
stated in
PubMed
page(s)
304-24
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stated in
PubMed
cites work
Mitochondrial DNA repair and aging
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
21 January 2018
THE RELATION OF RECOMBINATION TO MUTATIONAL ADVANCE
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
21 January 2018
In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
21 January 2018
In vitro analysis of mutations causing myoclonus epilepsy with ragged-red fibers in the mitochondrial tRNA(Lys)gene: two genotypes produce similar phenotypes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
21 January 2018
Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
21 January 2018
The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
21 January 2018
Novel Mitochondrial Transfer RNAPhe Gene Mutation Associated With Late-Onset Neuromuscular Disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new mitochondrial transfer RNAPro gene mutation associated with myoclonic epilepsy with ragged-red fibers and other neurological features
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Reintroduction of a characterized Mit tRNA glycine mutation into yeast mitochondria provides a new tool for the study of human neurodegenerative diseases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA mutations in human disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rescue of a mitochondrial deficiency causing Leber Hereditary Optic Neuropathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Aerobic conditioning in patients with mitochondrial myopathies: physiological, biochemical, and genetic effects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prevalence of mitochondrial DNA disease in adults
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Modulation of mitochondrial protein phosphorylation by soluble adenylyl cyclase ameliorates cytochrome oxidase defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pathogenic mitochondrial tRNA mutations--which mutations are inherited and why?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA molecules and virtual number of mitochondria per cell in mammalian cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exercise intolerance associated with a novel 8300T > C mutation in mitochondrial transfer RNAlys
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myoclonus epilepsy associated with ragged-red fibers: a G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNA(Lys) in two families.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial defects and hearing loss
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nucleotide substitution rate of mammalian mitochondrial genomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human mitochondrial tRNAs in health and disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sporadic myopathy and exercise intolerance associated with the mitochondrial 8328G>A tRNALys mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Does the mitochondrial genome play a role in the etiology of Alzheimer's disease?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis and manipulation of yeast mitochondrial genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pathogenic mitochondrial DNA mutations are common in the general population
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a new mtDNA mutation (14724G>A) associated with mitochondrial leukoencephalopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing loss
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
RETRACTED: Activation of the PPAR/PGC-1alpha pathway prevents a bioenergetic deficit and effectively improves a mitochondrial myopathy phenotype
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in yeast mt tRNAs: specific and general suppression by nuclear encoded tRNA interactors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Population prevalence of the MELAS A3243G mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Different effects of novel mtDNA G3242A and G3244A base changes adjacent to a common A3243G mutation in patients with mitochondrial disorders.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two novel cosegregating mutations in tRNAMet and COX III, in a patient with exercise intolerance and autoimmune polyendocrinopathy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Can yeast be used to study mitochondrial diseases? Biolistic tRNA mutants for the analysis of mechanisms and suppressors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
tRNA mitochondrial import in yeast: Mapping of the import determinants in the carrier protein, the precursor of mitochondrial lysyl-tRNA synthetase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Is selection required for the accumulation of somatic mitochondrial DNA mutations in post-mitotic cells?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial myopathy associated with a novel mutation in mtDNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Assigning pathogenicity to mitochondrial tRNA mutations: when "definitely maybe" is not good enough
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mitochondrial genome: structure, transcription, translation and replication
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNA(Lys) with the MERRF encephalomyopathy pathogenic mutation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Towards understanding human mitochondrial leucine aminoacylation identity.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Codon--anticodon pairing: the wobble hypothesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pathogenic expression of homoplasmic mtDNA mutations needs a complex nuclear-mitochondrial interaction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mammalian mitochondrial genetics: heredity, heteroplasmy and disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The crystal structure of Cys-tRNACys-EF-Tu-GDPNP reveals general and specific features in the ternary complex and in tRNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Wobble modification defect suppresses translational activity of tRNAs with MERRF and MELAS mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Search for characteristic structural features of mammalian mitochondrial tRNAs.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An aminoacyl-tRNA synthetase with a defunct editing site.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial genotype and clinical phenotype
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transfer of chloramphenicol-resistant mitochondrial DNA into the chimeric mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondria transfer into mouse ova by microinjection
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A different genetic code in human mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sequence and organization of the human mitochondrial genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
tRNA punctuation model of RNA processing in human mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial genome variation and the origin of modern humans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Initial sequencing and analysis of the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional consequences of mitochondrial tRNA Trp and tRNA Arg mutations causing combined OXPHOS defects.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Time dependency of molecular rate estimates for mtDNA: this is not the time for wishful thinking
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heteroplasmic mitochondrial DNA mutations in normal and tumour cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mitochondrial tRNA anticodon swap associated with a muscle disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mitochondrial bottleneck occurs without reduction of mtDNA content in female mouse germ cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mitochondrial DNA genetic bottleneck results from replication of a subpopulation of genomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rescue of a deficiency in ATP synthesis by transfer of MTATP6, a mitochondrial DNA-encoded gene, to the nucleus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA mutations in human disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Purifying selection of mtDNA and its implications for understanding evolution and mitochondrial disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A unique serine-specific elongation factor Tu found in nematode mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The yeast counterparts of human 'MELAS' mutations cause mitochondrial dysfunction that can be rescued by overexpression of the mitochondrial translation factor EF-Tu.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Concerted action of two novel tRNA mtDNA point mutations in chronic progressive external ophthalmoplegia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
CP1-dependent partitioning of pretransfer and posttransfer editing in leucyl-tRNA synthetase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Experimental evidence for kinetic proofreading in the aminoacylation of tRNA by synthetase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Different pattern of codon recognition by mammalian mitochondrial tRNAs
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA polymorphism in a maternal lineage of Holstein cows
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mammalian mitochondrial methionyl-tRNA transformylase from bovine liver. Purification, characterization, and gene structure.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Modification defect at anticodon wobble nucleotide of mitochondrial tRNAs(Leu)(UUR) with pathogenic mutations of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Recognition of tRNAs by Methionyl-tRNA transformylase from mammalian mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of editing activity during the evolution of mitochondrial phenylalanyl-tRNA synthetase.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A viable amino acid editing activity in the leucyl-tRNA synthetase CP1-splicing domain is not required in the yeast mitochondria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phylogenetic network for European mtDNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparative genomics and the evolution of human mitochondrial DNA: assessing the effects of selection
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inheritance of mitochondrial DNA recombinants in double-heteroplasmic families: potential implications for phylogenetic analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mitochondrial DNA transfer RNA(Lys)A-->G(8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF). Relationship of clinical phenotype to proportion of mutant mitochondrial DNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MELAS and MERRF. The relationship between maternal mutation load and the frequency of clinically affected offspring
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Wobble modification defect in tRNA disturbs codon-anticodon interaction in a mitochondrial disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gene shifting: a novel therapy for mitochondrial myopathy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heterologous mitochondrial DNA recombination in human cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Acquisition of the wobble modification in mitochondrial tRNALeu(CUN) bearing the G12300A mutation suppresses the MELAS molecular defect.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A functionally dominant mitochondrial DNA mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The A3243G tRNALeu(UUR) MELAS mutation causes amino acid misincorporation and a combined respiratory chain assembly defect partially suppressed by overexpression of EFTu and EFG2.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fine mapping of mitochondrial RNAs derived from the mtDNA region containing a point mutation associated with MELAS
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MITOMAP: an update on the status of the human mitochondrial genome database
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Universal rules and idiosyncratic features in tRNA identity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effect of a mutation in the anticodon of human mitochondrial tRNAPro on its post-transcriptional modification pattern
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The presence of modified nucleotides is required for cloverleaf folding of a human mitochondrial tRNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Interaction of mitochondrial initiation factor 2 with mitochondrial fMet-tRNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new mechanism for mtDNA pathogenesis: impairment of post-transcriptional maturation leads to severe depletion of mitochondrial tRNASer(UCN) caused by T7512C and G7497A point mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Overexpression of human mitochondrial valyl tRNA synthetase can partially restore levels of cognate mt-tRNAVal carrying the pathogenic C25U mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The causes of mutation accumulation in mitochondrial genomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
How is the mouse germ-cell lineage established?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation in the mitochondrial tRNA for tryptophan causing a late-onset mitochondrial encephalomyopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mouse model of mitochondrial disease reveals germline selection against severe mtDNA mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Medicine. Sidestepping mutational meltdown
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hungry codons promote frameshifting in human mitochondrial ribosomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Models of human evolution
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial diseases in man and mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Suppression of mutations in mitochondrial DNA by tRNAs imported from the cytoplasm
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Fidelity of mammalian DNA polymerases
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ribonuclease P: unity and diversity in a tRNA processing ribozyme
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular genetic aspects of human mitochondrial disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial DNA and human evolution.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pure myopathy associated with a novel mitochondrial tRNA gene mutation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Overexpressed mitochondrial leucyl-tRNA synthetase suppresses the A3243G mutation in the mitochondrial tRNA(Leu(UUR)) gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mamit-tRNA, a database of mammalian mitochondrial tRNA primary and secondary structures
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Yeast as a model of human mitochondrial tRNA base substitutions: investigation of the molecular basis of respiratory defects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Strong purifying selection in transmission of mammalian mitochondrial DNA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
New evidence confirms that the mitochondrial bottleneck is generated without reduction of mitochondrial DNA content in early primordial germ cells of mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The role of selection in the evolution of human mitochondrial genomes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular epidemiology of childhood mitochondrial encephalomyopathies in a Finnish population: sequence analysis of entire mtDNA of 17 children reveals heteroplasmic mutations in tRNAArg, tRNAGlu, and tRNALeu(UUR) genes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mitochondrial tRNA mutations: clinical and functional perturbations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FWRNA.27
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1002/WRNA.27
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1305390
OpenCitations bibliographic resource ID
1305390
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1305390
PubMed publication ID
21935892
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1305390
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