Microscale oxygraphy reveals OXPHOS impairment in MRC mutant cells (Q28730871)

1

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Valeria Tiranti

object named as

V Tiranti

6

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author name string

P B Jensen

3

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S Ravaglia

4

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M Zeviani

High throughput microplate respiratory measurements using minimal quantities of isolated mitochondria

5

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language of work or name

English

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publication date

March 2012

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published in

Mitochondrion

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volume

12

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issue

2

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page(s)

328-35

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cites work

1 reference

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Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies

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Biochemical diagnosis of mitochondrial disorders

17 March 2017

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The mtDNA T8993G (NARP) mutation results in an impairment of oxidative phosphorylation that can be improved by antioxidants

17 March 2017

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The effects of idebenone on mitochondrial bioenergetics

17 March 2017

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Assessing mitochondrial dysfunction in cells.

3 June 2018

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Mitochondrial DNA background modifies the bioenergetics of NARP/MILS ATP6 mutant cells

3 June 2018

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Supramolecular organization of ATP synthase and respiratory chain in mitochondrial membranes

3 June 2018

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Respiratory active mitochondrial supercomplexes.

3 June 2018

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Severe infantile encephalomyopathy caused by a mutation in COX6B1, a nucleus-encoded subunit of cytochrome c oxidase

3 June 2018

1 reference

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Biochemical assays of respiratory chain complex activity

3 June 2018

1 reference

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Impaired complex III assembly associated with BCS1L gene mutations in isolated mitochondrial encephalopathy

3 June 2018

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Mitochondrial medicine: a metabolic perspective on the pathology of oxidative phosphorylation disorders

3 June 2018

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Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency

3 June 2018

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The ATP synthase is involved in generating mitochondrial cristae morphology

3 June 2018

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Biochemical consequences in yeast of the human mitochondrial DNA 8993T>C mutation in the ATPase6 gene found in NARP/MILS patients

3 June 2018

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Identification of novel mutations in five patients with mitochondrial encephalomyopathy.

27 November 2018

1 reference

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Clinical and molecular findings in children with complex I deficiency

27 November 2018

1 reference

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Biochemical and molecular investigations in respiratory chain deficiencies

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22310368

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Three spectrophotometric assays for the measurement of the five respiratory chain complexes in minuscule biological samples

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22310368

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22310368

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.MITO.2012.01.001

1 reference

512177

512177

1 reference

1 reference

1 reference