scholarly article | Q13442814 |
P50 | author | Arnaud Mourier | Q56944202 |
Laura C Greaves | Q61806634 | ||
Robert William Taylor | Q89929096 | ||
James Bruce Stewart | Q42048741 | ||
P2093 | author name string | Marie-Lune Simard | |
P2860 | cites work | A valid quantitative histochemical technique for assaying cytochrome c oxidase in single cells. | Q43671464 |
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Quantitative mapping of cytochrome oxidase activity in the central auditory system of the gerbil: a study with calibrated activity standards and metal-intensified histochemistry | Q72424991 | ||
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Histochemical localization of specific oxidative enzymes. V. The dissociation of succinic dehydrogenase from carriers by lipase and the specific histochemical localization of the dehydrogenase with phenazine methosulfate and tetrazolium salts | Q74160057 | ||
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EFFECTS OF PHENAZINE METHOSULFATE IN HISTOCHEMISTRY | Q77166508 | ||
A colorimetric method for the estimation of succinic dehydrogenase activity | Q78844466 | ||
Increased longevity and refractoriness to Ca(2+)-dependent neurodegeneration in Surf1 knockout mice | Q79518243 | ||
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Premature ageing in mice expressing defective mitochondrial DNA polymerase | Q24294365 | ||
LRPPRC is necessary for polyadenylation and coordination of translation of mitochondrial mRNAs | Q24295176 | ||
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Constitutive knockout of Surf1 is associated with high embryonic lethality, mitochondrial disease and cytochrome c oxidase deficiency in mice | Q28507157 | ||
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Drosophila melanogaster LRPPRC2 is involved in coordination of mitochondrial translation | Q34711876 | ||
Human stem cell aging: do mitochondrial DNA mutations have a causal role? | Q35093139 | ||
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A novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis. | Q36164488 | ||
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Modeling human mitochondrial diseases in flies | Q36522081 | ||
The mitochondrial energy transduction system and the aging process | Q36614262 | ||
Complementation between polymerase- and exonuclease-deficient mitochondrial DNA polymerase mutants in genomically engineered flies | Q36638620 | ||
Mitochondrial disease in childhood: mtDNA encoded | Q36762842 | ||
Brain mitochondrial dysfunction in aging | Q37141862 | ||
Germline mitochondrial DNA mutations aggravate ageing and can impair brain development | Q37288018 | ||
A Phenotype-Driven Approach to Generate Mouse Models with Pathogenic mtDNA Mutations Causing Mitochondrial Disease. | Q37289982 | ||
The genetics and pathology of mitochondrial disease. | Q37560946 | ||
Genetic and biochemical intricacy shapes mitochondrial cytopathies. | Q38356644 | ||
Loss of LRPPRC causes ATP synthase deficiency | Q38806341 | ||
Enzyme detection using phenazine methosulphate and tetrazolium salts: Interference by oxygen | Q39150024 | ||
An accurate method for the quantification of cytochrome C oxidase in tissue sections | Q40391409 | ||
P433 | issue | 3 | |
P304 | page(s) | 311-323 | |
P577 | publication date | 2018-05-14 | |
P1433 | published in | Journal of Pathology | Q400296 |
P1476 | title | A novel histochemistry assay to assess and quantify focal cytochrome c oxidase deficiency | |
P478 | volume | 245 |
Q61809068 | Mitochondrial Heterogeneity | cites work | P2860 |
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