(Q39326113)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728747%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

title

Fluorescence imaging of mitochondria in cultured skin fibroblasts: a useful method for the detection of oxidative phosphorylation defects (English)

1 reference

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6 February 2020

0 references

1 reference

2

1 reference

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6 February 2020

Willy Lissens

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728747%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Dieter Deforce

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728747%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Richard J Rodenburg

9

1 reference

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6 February 2020

author name string

Boel De Paepe

1

1 reference

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6 February 2020

Arnaud Vanlander

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728747%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Sara Seneca

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728747%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Linda De Meirleir

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728747%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

Mado Vandewoestyne

7

1 reference

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6 February 2020

Rudy Van Coster

10

1 reference

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6 February 2020

language of work or name

English

0 references

publication date

22 June 2012

1 reference

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6 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728747%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

volume

72

1 reference

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6 February 2020

issue

3

1 reference

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6 February 2020

page(s)

232-240

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22728747%20AND%20SRC:MED&resulttype=core&format=json

ATP synthesis by F-type ATP synthase is obligatorily dependent on the transmembrane voltage

6 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Deficiency of respiratory chain complex I is a common cause of Leigh disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Mitochondrial DNA depletion syndromes--many genes, common mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

The oxidative phosphorylation (OXPHOS) system: nuclear genes and human genetic diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Mitochondrial Ca2+ homeostasis in human NADH:ubiquinone oxidoreductase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Calcium and ATP handling in human NADH:ubiquinone oxidoreductase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Rotenone inhibits mammalian cell proliferation by inhibiting microtubule assembly through tubulin binding

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Vimentin supports mitochondrial morphology and organization

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Cytoskeletal structure of myoblasts with the mitochondrial DNA 3243A-->G mutation and of osteosarcoma cells with respiratory chain deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Proteome and cytoskeleton responses in osteosarcoma cells with reduced OXPHOS activity

21 January 2018

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https://api.crossref.org/works/10.1038%2FPR.2012.84

Mitochondrial dynamics in human NADH:ubiquinone oxidoreductase deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Single cell quantification of the 8993T>G NARP mitochondrial DNA mutation by fluorescent PCR

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Polar body mutation load analysis in a patient with A3243G tRNALeu(UUR) point mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Homozygous Gly555Glu mutation in the nuclear-encoded 70 kDa flavoprotein gene causes instability of the respiratory chain complex II

21 January 2018

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https://api.crossref.org/works/10.1038%2FPR.2012.84

Respiratory chain complex V deficiency due to a mutation in the assembly gene ATP12

21 January 2018

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A novel mitochondrial transfer RNA(Asn) mutation causing multiorgan failure.

21 January 2018

1 reference

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A new family with the mitochondrial tRNAGLU gene mutation m.14709T>C presenting with hydrops fetalis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Cytochrome c oxidase deficiency in Leigh syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Blue native polyacrylamide gel electrophoresis: a powerful tool in diagnosis of oxidative phosphorylation defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Diagnostic value of immunostaining in cultured skin fibroblasts from patients with oxidative phosphorylation defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Intracellular heterogeneity in mitochondrial membrane potentials revealed by a J-aggregate-forming lipophilic cation JC-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

J-aggregate formation of a carbocyanine as a quantitative fluorescent indicator of membrane potential

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Suspension fluorescence in situ hybridization (S-FISH) combined with automatic detection and laser microdissection for STR profiling of male cells in male/female mixtures

21 January 2018

1 reference

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Intracellular transport: ER and mitochondria meet and greet along designated tracks

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Titrating the effects of mitochondrial complex I impairment in the cell physiology

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Infantile presentation of the mitochondrial A8344G mutation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

A mitochondrial tRNA aspartate mutation causing isolated mitochondrial myopathy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84

Biochemical and molecular investigations in respiratory chain deficiencies

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FPR.2012.84