(Q39937507)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18806273%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

title

Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease (English)

1 reference

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14 January 2020

0 references

1 reference

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14 January 2020

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14 January 2020

1 reference

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14 January 2020

1 reference

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14 January 2020

1 reference

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14 January 2020

1 reference

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14 January 2020

1 reference

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14 January 2020

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14 January 2020

Antonio Torroni

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18806273%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

Rosa Pello

1 reference

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14 January 2020

Leo G Nijtmans

series ordinal

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14 January 2020

Eduardo Ruiz-Pesini

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18806273%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

Jan A Smeitink

series ordinal

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14 January 2020

publication date

19 September 2008

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14 January 2020

published in

Human Molecular Genetics

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14 January 2020

volume

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14 January 2020

issue

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14 January 2020

page(s)

4001-4011

1 reference

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Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

14 January 2020

cites work

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Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.

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Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background

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Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

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Mitochondrial dysfunction as a cause of optic neuropathies

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

21 January 2018

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Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation

21 January 2018

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Severe impairment of complex I-driven adenosine triphosphate synthesis in leber hereditary optic neuropathy cybrids

21 January 2018

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Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells

21 January 2018

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Leber hereditary optic neuropathy mtDNA mutations disrupt glutamate transport in cybrid cell lines.

21 January 2018

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Antioxidant defences in cybrids harboring mtDNA mutations associated with Leber's hereditary optic neuropathy

21 January 2018

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Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose medium

21 January 2018

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

21 January 2018

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Human mitochondrial complex I assembles through the combination of evolutionary conserved modules: a framework to interpret complex I deficiencies.

21 January 2018

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Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiency

21 January 2018

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Development and characterization of a conditional mitochondrial complex I assembly system

21 January 2018

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Analysis of the assembly profiles for mitochondrial- and nuclear-DNA-encoded subunits into complex I

21 January 2018

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Respiratory function in cybrid cell lines carrying European mtDNA haplogroups: implications for Leber's hereditary optic neuropathy

21 January 2018

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Experimental assessment of bioenergetic differences caused by the common European mitochondrial DNA haplogroups H and T.

21 January 2018

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Significance of respirasomes for the assembly/stability of human respiratory chain complex I.

21 January 2018

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Respiratory complex III is required to maintain complex I in mammalian mitochondria

21 January 2018

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Cytochrome c oxidase is required for the assembly/stability of respiratory complex I in mouse fibroblasts

21 January 2018

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A novel mtDNA ND6 gene mutation associated with LHON in a Caucasian family

21 January 2018

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Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

21 January 2018

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Rescue of a mitochondrial deficiency causing Leber Hereditary Optic Neuropathy

21 January 2018

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Differences in reactive oxygen species production explain the phenotypes associated with common mouse mitochondrial DNA variants

21 January 2018

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The molecular dissection of mtDNA haplogroup H confirms that the Franco-Cantabrian glacial refuge was a major source for the European gene pool

21 January 2018

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Human mtDNA haplogroups associated with high or reduced spermatozoa motility

21 January 2018

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Peginterferon alpha-2b plus ribavirin vs interferon alpha-2b plus ribavirin for chronic hepatitis C in HIV-coinfected patients

21 January 2018

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Blue Native electrophoresis to study mitochondrial and other protein complexes

21 January 2018

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