(Q36164488)

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A novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis.

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scholarly article

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26469001%20AND%20SRC:MED&resulttype=core&format=json

27 February 2020

A novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26469001%20AND%20SRC:MED&resulttype=core&format=json

27 February 2020

immunofluorescence microscopy

1 reference

based on heuristic

inferred from title

phosphorylation

1 reference

based on heuristic

inferred from title

mitochondrial myopathy

1 reference

based on heuristic

inferred from title

Mariana C Rocha

1

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27 February 2020

2

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27 February 2020

4

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27 February 2020

Douglass Matthew Turnbull

7

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27 February 2020

Robert William Taylor

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Robert W Taylor

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27 February 2020

Karolina A Rygiel

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Karolina A Rygiel

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27 February 2020

Anne Grünewald

3

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Anne Grünewald

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27 February 2020

author name string

Philip F Dobson

5

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27 February 2020

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15 October 2015

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27 February 2020

Scientific Reports

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27 February 2020

5

1 reference

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27 February 2020

15037

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27 February 2020

copyright license

Creative Commons Attribution 4.0 International

15 October 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

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https://scigraph.springernature.com/pub.10.1038/srep15037

0 references

Triplex real-time PCR--an improved method to detect a wide spectrum of mitochondrial DNA deletions in single cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Novel MTND1 mutations cause isolated exercise intolerance, complex I deficiency and increased assembly factor expression.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Mitochondrial myopathies in adults and children: management and therapy development.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Quantitative quadruple-label immunofluorescence of mitochondrial and cytoplasmic proteins in single neurons from human midbrain tissue

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Mitochondrial and inflammatory changes in sporadic inclusion body myositis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Dissecting the mechanisms underlying the accumulation of mitochondrial DNA deletions in human skeletal muscle.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Disease progression in patients with single, large-scale mitochondrial DNA deletions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

A comparison between manual and automated evaluations of tissue microarray patterns of protein expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Automated image analysis of skeletal muscle fiber cross-sectional area

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Adults with RRM2B-related mitochondrial disease have distinct clinical and molecular characteristics.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Quantitative comparison of immunohistochemical staining measured by digital image analysis versus pathologist visual scoring

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Respiratory chain complex I deficiency caused by mitochondrial DNA mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

A neurological perspective on mitochondrial disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

A robust automated measure of average antibody staining in immunohistochemistry images

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Accuracy of dementia diagnosis: a direct comparison between radiologists and a computerized method

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Assembly of the oxidative phosphorylation system in humans: what we have learned by studying its defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Assembly of mitochondrial complex I and defects in disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Biochemical assays of respiratory chain complex activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Mitochondrial complex I: structure, function and pathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Digital image analysis for the evaluation of the inflammatory infiltrate in psoriasis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

The role of the LRPPRC (leucine-rich pentatricopeptide repeat cassette) gene in cytochrome oxidase assembly: mutation causes lowered levels of COX (cytochrome c oxidase) I and COX III mRNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

The diagnosis of mitochondrial muscle disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

An immunocytochemical approach to detection of mitochondrial disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Isolated complex I deficiency in children: clinical, biochemical and genetic aspects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

A biochemically distinct form of cytochrome oxidase (COX) deficiency in the Saguenay-Lac-Saint-Jean region of Quebec

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Mitochondrial cytopathy. A multisystem disorder with ragged red fibres on muscle biopsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 October 2017

Altered mitochondrial function in fibroblasts containing MELAS or MERRF mitochondrial DNA mutations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 July 2018

Methods of microphotometric assay of succinate dehydrogenase and cytochrome c oxidase activities for use on human skeletal muscle.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 July 2018

Segmental cytochrome c‐oxidase deficiency in CPEO: Teased muscle fiber analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

2 July 2018

The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis and management.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

23 September 2018

Mitochondrial DNA deletions and neurodegeneration in multiple sclerosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

23 September 2018

Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

23 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

23 September 2018

Nature of mitochondrial DNA deletions in substantia nigra neurons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

23 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

23 September 2018

Mutations of the mitochondrial ND1 gene as a cause of MELAS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

23 September 2018

Spontaneous recovery of a childhood onset mitochondrial myopathy caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

23 September 2018

Automated selection of DAB-labeled tissue for immunohistochemical quantification.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

23 September 2018

HER-2/neu in breast cancer: interobserver variability and performance of immunohistochemistry with 4 antibodies compared with fluorescent in situ hybridization.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

23 September 2018

Mitochondrial DNA deletions in inclusion body myositis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

23 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4606788

23 September 2018

An analysis of variance test for normality (complete samples)

1 reference

https://api.crossref.org/works/10.1038%2FSREP15037

21 January 2018

Clinical progression of mitochondrial myopathy is associated with the random accumulation of cytochrome c oxidase negative skeletal muscle fibres

1 reference

https://pubmed.ncbi.nlm.nih.gov/26469001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres

1 reference

https://pubmed.ncbi.nlm.nih.gov/26469001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/26469001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytochemistry and immunocytochemistry of mitochondria in tissue sections

1 reference

https://pubmed.ncbi.nlm.nih.gov/26469001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial Encephalomyopathy Associated with a Novel Mutation in the Mitochondrial tRNAleu(UUR)Gene (A3243T)

1 reference

https://pubmed.ncbi.nlm.nih.gov/26469001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential diagnosis of fatal and benign cytochrome c oxidase-deficient myopathies of infancy: an immunohistochemical approach

1 reference

https://pubmed.ncbi.nlm.nih.gov/26469001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of cytochrome c oxidase activity and mitochondrial proteins in single cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/26469001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial DNA and disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/26469001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytochrome oxidase immunohistochemistry: clues for genetic mechanisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/26469001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/26469001

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/SREP15037

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26469001%20AND%20SRC:MED&resulttype=core&format=json

27 February 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26469001%20AND%20SRC:MED&resulttype=core&format=json

27 February 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26469001%20AND%20SRC:MED&resulttype=core&format=json

27 February 2020

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