(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

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

14 January 2020

0 references

1 reference

5

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

Maria Pala

6

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

Miguel Angel Martín

2

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

Valerio Carelli

3

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

Aurora Gomez-Duran

8

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

Andrea Martinuzzi

10

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

Joaquín Arenas

12

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

Cristina Ugalde

13

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

7

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

author name string

Rosa Pello

1

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

Leo G Nijtmans

4

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

Eduardo Ruiz-Pesini

9

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

11

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

publication date

19 September 2008

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

published in

Human Molecular Genetics

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

volume

17

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

issue

24

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

page(s)

4001-4011

1 reference

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

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

14 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

Mitochondrial dysfunction as a cause of optic neuropathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

Development and characterization of a conditional mitochondrial complex I assembly system

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

Rescue of a mitochondrial deficiency causing Leber Hereditary Optic Neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

Human mtDNA haplogroups associated with high or reduced spermatozoa motility

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303

Blue Native electrophoresis to study mitochondrial and other protein complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN303