(Q40831709)

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Very rare complementation between mitochondria carrying different mitochondrial DNA mutations points to intrinsic genetic autonomy of the organelles in cultured human cells.

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10753928%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

Very rare complementation between mitochondria carrying different mitochondrial DNA mutations points to intrinsic genetic autonomy of the organelles in cultured human cells (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10753928%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

mitochondrial DNA

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José Antonio Enríquez

1

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Europe PubMed Central

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5 November 2019

Juan Cabezas-Herrera

2

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Europe PubMed Central

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5 November 2019

Juan Cabezas-Herrera

3

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5 November 2019

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M P Bayona-Bafaluy

4

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5 November 2019

G Attardi

5

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5 November 2019

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1 April 2000

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5 November 2019

Journal of Biological Chemistry

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5 November 2019

275

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5 November 2019

15

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5 November 2019

11207-11215

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5 November 2019

Complementation in cytoplasmic petite mutants of yeast to form respiratory competent cells

1 reference

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Transmission of mitochondrial and chloroplast genomes in crosses of Chlamydomonas

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The structure of rat liver mitochondria: a reevaluation.

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Dynamics of mitochondria in living cells: shape changes, dislocations, fusion, and fission of mitochondria

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Close contacts with the endoplasmic reticulum as determinants of mitochondrial Ca2+ responses

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Developmentally regulated mitochondrial fusion mediated by a conserved, novel, predicted GTPase.

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Fzo1p is a mitochondrial outer membrane protein essential for the biogenesis of functional mitochondria in Saccharomyces cerevisiae

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Mitochondrial fusion in yeast requires the transmembrane GTPase Fzo1p

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Structural organization of surface domains of sperm mitochondria

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Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell within distinct organelles

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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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A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).

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A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

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Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

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21 January 2018

Human mitochondria and mitochondrial genome function as a single dynamic cellular unit

1 reference

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21 January 2018

Transcomplementation between different types of respiration-deficient mitochondria with different pathogenic mutant mitochondrial DNAs

1 reference

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21 January 2018

In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria

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Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction

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Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy

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Efficient selection and characterization of mutants of a human cell line which are defective in mitochondrial DNA-encoded subunits of respiratory NADH dehydrogenase

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21 January 2018

Analysis of aminoacylation of human mitochondrial tRNAs

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21 January 2018

MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination

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21 January 2018

The selection of Chinese hamster cells deficient in oxidative energy metabolism

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21 January 2018

Nonviability of cells with oxidative defects in galactose medium: a screening test for affected patient fibroblasts

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21 January 2018

Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation

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21 January 2018

Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathy

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21 January 2018

The mtDNA-encoded ND6 subunit of mitochondrial NADH dehydrogenase is essential for the assembly of the membrane arm and the respiratory function of the enzyme

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21 January 2018

Ethidium bromide-induced loss of mitochondrial DNA from primary chicken embryo fibroblasts

1 reference

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21 January 2018

Tight control of respiration by NADH dehydrogenase ND5 subunit gene expression in mouse mitochondria

1 reference

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21 January 2018

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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21 January 2018

Injection of mitochondria into human cells leads to a rapid replacement of the endogenous mitochondrial DNA.

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21 January 2018

In vivo control of respiration by cytochrome c oxidase in wild-type and mitochondrial DNA mutation-carrying human cells

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21 January 2018

Mitochondrial DNA sequence variation in human evolution and disease.

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21 January 2018

Oxidative damage and mitochondrial decay in aging

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Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain

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

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Multiple mitochondrial DNA deletions in an elderly human individual.

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

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Human mitochondria: distinct organelles or dynamic network?

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Intergenomic recombination of mitochondrial genomes in a somatic hybrid plant

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Intermitochondrial contacts in myocardiocytes

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The interorganellar interaction between distinct human mitochondria with deletion mutant mtDNA from a patient with mitochondrial disease and with HeLa mtDNA

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