(Q46174978)

English

Aberrant synthesis of ATP synthase resulting from a novel deletion in mitochondrial DNA in an African patient with progressive external ophthalmoplegia

scientific article published on 16 January 2010

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/20082143

Aberrant synthesis of ATP synthase resulting from a novel deletion in mitochondrial DNA in an African patient with progressive external ophthalmoplegia (English)

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/20082143

mitochondrial DNA

0 references

2

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/20082143

author name string

Francois H van der Westhuizen

1

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/20082143

Oksana Levanets

3

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/20082143

Madelein Meissner-Roloff

4

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/20082143

Roan Louw

5

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/20082143

Rudy Van Coster

6

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/20082143

Izelle Smuts

7

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/20082143

publication date

16 January 2010

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/20082143

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/20082143

33 Suppl 3

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/20082143

S55-62

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/20082143

https://scigraph.springernature.com/pub.10.1007/s10545-009-9020-y

0 references

Simultaneous detection and quantification of mitochondrial DNA deletion(s), depletion, and over-replication in patients with mitochondrial disease

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Brain magnetic resonance imaging findings in patients with mitochondrial cytopathies.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Brain magnetic resonance in the diagnostic evaluation of mitochondrial encephalopathies.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

MRI of the brain in the Kearns-Sayre syndrome: report of four cases and a review

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Linezolid-induced inhibition of mitochondrial protein synthesis.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Mass spectrometric identification of mitochondrial oxidative phosphorylation subunits separated by two-dimensional blue-native polyacrylamide gel electrophoresis

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Chronic progressive external ophthalmoplegia: MR spectroscopy and MR diffusion studies in the brain.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Mitochondrial biogenesis and mitochondrial DNA maintenance of mammalian cells under oxidative stress.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

White matter involvement in mitochondrial diseases

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Mitochondrial DNA-related disorders

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Oxidative stress and upregulation of mitochondrial biogenesis genes in mitochondrial DNA-depleted HeLa cells

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Molecular diagnosis of Alpers syndrome.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Relative expression software tool (REST©) for group-wise comparison and statistical analysis of relative expression results in real-time PCR

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Leigh syndrome: clinical features and biochemical and DNA abnormalities.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Two direct repeats cause most human mtDNA deletions

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Neuroimaging of mitochondrial disease.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

The kinetic properties of citrate synthase from rat liver mitochondria

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Subcomplexes of mitochondrial complex V reveal mutations in mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Genotype and phenotype analyses in 136 patients with single large-scale mitochondrial DNA deletions.

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

Subcomplexes of human ATP synthase mark mitochondrial biosynthesis disorders

1 reference

https://api.crossref.org/works/10.1007%2FS10545-009-9020-Y

21 January 2018

MR of the brain in mitochondrial myopathy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20082143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An improved spectrophotometric assay of pyruvate dehydrogenase in lactate dehydrogenase contaminated mitochondrial preparations from human skeletal muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/20082143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebral MR in ophthalmoplegia plus.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20082143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mitochondrial genome: structure, transcription, translation and replication

1 reference

https://pubmed.ncbi.nlm.nih.gov/20082143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrophotometric Assay for Complex I of the Respiratory Chain in Tissue Samples and Cultured Fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/20082143

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10545-009-9020-Y

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/20082143

1 reference

Europe PubMed Central

20 December 2017

http://europepmc.org/abstract/MED/20082143

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q46174978&oldid=2097452418"