The determination of complete human mitochondrial DNA sequences in single cells: implications for the study of somatic mitochondrial DNA point mutations (Q39096996)

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scientific article published on August 2001

Language	Label	Description	Also known as
English	The determination of complete human mitochondrial DNA sequences in single cells: implications for the study of somatic mitochondrial DNA point mutations	scientific article published on August 2001

Statements

scholarly article

1 reference

Europe PubMed Central

9 September 2017

The determination of complete human mitochondrial DNA sequences in single cells: implications for the study of somatic mitochondrial DNA point mutations (English)

1 reference

Europe PubMed Central

9 September 2017

mitochondrial DNA

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author name string

Taylor RW

1

1 reference

Europe PubMed Central

9 September 2017

Taylor GA

2

1 reference

Europe PubMed Central

9 September 2017

Durham SE

3

1 reference

Europe PubMed Central

9 September 2017

Turnbull DM

4

1 reference

Europe PubMed Central

9 September 2017

language of work or name

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publication date

1 August 2001

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Europe PubMed Central

9 September 2017

Nucleic Acids Research

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Europe PubMed Central

9 September 2017

29

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Europe PubMed Central

9 September 2017

E74-4

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Europe PubMed Central

9 September 2017

15

1 reference

Europe PubMed Central

9 September 2017

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC55839/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Cytochrome c oxidase deficient cells accumulate in the hippocampus and choroid plexus with age.

1 reference

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Simultaneous A8344G heteroplasmy and mitochondrial DNA copy number quantification in myoclonus epilepsy and ragged-red fibers (MERRF) syndrome by a multiplex molecular beacon based real-time fluorescence PCR.

1 reference

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Analysis of European mtDNAs for recombination

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9 September 2017

The age-related accumulation of a mitochondrial DNA control region mutation in muscle, but not brain, detected by a sensitive PNA-directed PCR clamping based method

1 reference

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Facile detection of mitochondrial DNA mutations in tumors and bodily fluids

1 reference

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9 September 2017

Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication

1 reference

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9 September 2017

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

1 reference

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An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy

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Somatic mutations of the mitochondrial genome in human colorectal tumours

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Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.

1 reference

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Apparent mtDNA heteroplasmy in Alzheimer's disease patients and in normals due to PCR amplification of nucleus-embedded mtDNA pseudogenes

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Mutations in mitochondrial cytochrome c oxidase genes segregate with late-onset Alzheimer disease

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Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brain.

1 reference

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Sequence and organization of the human mitochondrial genome

1 reference

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Normal oxidative damage to mitochondrial and nuclear DNA is extensive

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=55839

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Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

1 reference

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Detection of a specific mitochondrial DNA deletion in tissues of older humans

1 reference

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Nuclear gadgets in mitochondrial DNA replication and transcription

1 reference

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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

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Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF)

1 reference

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Complementation and segregation behavior of disease-causing mitochondrial DNA mutations in cellular model systems

1 reference

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14 September 2017

Point mutations of the mtDNA control region in normal and neurodegenerative human brains

1 reference

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Mammalian mitochondrial genetics: heredity, heteroplasmy and disease

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Mitochondrial DNA mutations and pathogenesis

1 reference

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Methods of microphotometric assay of succinate dehydrogenase and cytochrome c oxidase activities for use on human skeletal muscle.

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Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age

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Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene.

1 reference

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Clinical features, investigation, and management of patients with defects of mitochondrial DNA.

1 reference

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Myoclonic epilepsy and ragged red fibers (MERRF) syndrome: selective vulnerability of CNS neurons does not correlate with the level of mitochondrial tRNAlys mutation in individual neuronal isolates.

1 reference

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Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/11470889

12 December 2020

based on heuristic

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Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia

1 reference

https://pubmed.ncbi.nlm.nih.gov/11470889

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inferred from PubMed ID database lookup

Role of mitochondrial DNA mutations in human aging: implications for the central nervous system and muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/11470889

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Mitochondrial enzyme activity in amyotrophic lateral sclerosis: implications for the role of mitochondria in neuronal cell death

1 reference

https://pubmed.ncbi.nlm.nih.gov/11470889

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based on heuristic

inferred from PubMed ID database lookup

The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS

1 reference

https://pubmed.ncbi.nlm.nih.gov/11470889

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based on heuristic

inferred from PubMed ID database lookup

Quantification and sequencing of somatic deleted mtDNA in single cells: evidence for partially duplicated mtDNA in aged human tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/11470889

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based on heuristic

inferred from PubMed ID database lookup

Study of mitochondrial DNA depletion in muscle by single-fiber polymerase chain reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/11470889

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based on heuristic

inferred from PubMed ID database lookup

Diagnosis of mitochondrial disease: assessment of mitochondrial DNA heteroplasmy in blood

1 reference

https://pubmed.ncbi.nlm.nih.gov/11470889

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Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/11470889

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based on heuristic

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Identifiers

10.1093/NAR/29.15.E74

1 reference

Europe PubMed Central

9 September 2017

1 reference

Europe PubMed Central

9 September 2017

1 reference

Europe PubMed Central

9 September 2017

ResearchGate publication ID

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