Cytochrome c oxidase-intermediate fibres: importance in understanding the pathogenesis and treatment of mitochondrial myopathy (Q36333507)

13 August 2017

Cytochrome c oxidase-intermediate fibres: importance in understanding the pathogenesis and treatment of mitochondrial myopathy (English)

1 reference

13 August 2017

0 references

mitochondrial myopathy

1 reference

7

Tanja Taivassalo

1 reference

13 August 2017

5

Emma L Blakely

1 reference

13 August 2017

Robert William Taylor

9

object named as

Robert W Taylor

1 reference

13 August 2017

Julie L Murphy

1

1 reference

13 August 2017

Thiloka E Ratnaike

2

1 reference

13 August 2017

Ersong Shang

3

1 reference

13 August 2017

Gavin Falkous

4

1 reference

13 August 2017

Charlotte L Alston

6

1 reference

13 August 2017

Ronald G Haller

8

1 reference

13 August 2017

Doug M Turnbull

10

1 reference

13 August 2017

28 May 2012

1 reference

13 August 2017

Neuromuscular Disorders

1 reference

13 August 2017

22

1 reference

13 August 2017

8

1 reference

13 August 2017

690-698

1 reference

Five entry points of the mitochondrially encoded subunits in mammalian complex I assembly

13 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3476534

Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3476534

Normal levels of wild-type mitochondrial DNA maintain cytochrome c oxidase activity for two pathogenic mitochondrial DNA mutations but not for m.3243A-->G.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3476534

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3476534

Mitochondrial DNA mutations in human disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3476534

The diagnosis of mitochondrial muscle disease.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3476534

Mitochondrial DNA mutations in human colonic crypt stem cells

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3476534

Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3476534

Sequence and organization of the human mitochondrial genome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3476534

Muscle fiber types: how many and what kind?

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3476534

Resistance training in patients with single, large-scale deletions of mitochondrial DNA.

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3476534

Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletions.

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3476534

Immunological approaches to the characterization and diagnosis of mitochondrial disease

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3476534

Mitochondrial DNA copy number threshold in mtDNA depletion myopathy

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3476534

Presentation and clinical investigation of mitochondrial respiratory chain disease. A study of 51 patients

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3476534

A partial deficiency of cytochrome c oxidase in chronic progressive external ophthalmoplegia.

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3476534

Aerobic conditioning in patients with mitochondrial myopathies: physiological, biochemical, and genetic effects

22 September 2018

1 reference

12 December 2020

Cytochemistry and immunocytochemistry of mitochondria in tissue sections

1 reference

12 December 2020

The length of cytochrome c oxidase-negative segments in muscle fibres in patients with mtDNA myopathy

1 reference

12 December 2020

Increased axonal mitochondrial activity as an adaptation to myelin deficiency in the Shiverer mouse

1 reference

12 December 2020

Cytochromec oxidase activity in single muscle fibers: Assay techniques and diagnostic applications

1 reference

12 December 2020

A multiplex real-time PCR method to detect and quantify mitochondrial DNA deletions in individual cells

1 reference

12 December 2020

10.1016/J.NMD.2012.04.003

Identifiers

DOI

1 reference

release_hj7no7jbrrbdvof2qqh3n3p7am

13 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/hj7no7jbrrbdvof2qqh3n3p7am

24 November 2022

mapped directly with Wikidata item

1 reference

13 August 2017

PubMed publication ID

22647770

1 reference