| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1004978032 |
| P356 | DOI | 10.1023/A:1005643508075 |
| P698 | PubMed publication ID | 10604144 |
| P2093 | author name string | J M Land | |
| S J Heales | |||
| I P Hargreaves | |||
| P2860 | cites work | Protein measurement with the Folin phenol reagent | Q20900776 |
| Hydroperoxide metabolism in mammalian organs | Q29614205 | ||
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| Disorders of the electron transport chain | Q41180826 | ||
| Neurological presentations of mitochondrial diseases | Q41180852 | ||
| Morphological studies of skeletal muscle in lactic acidosis | Q41180866 | ||
| Generation of superoxide anion by the NADH dehydrogenase of bovine heart mitochondria | Q41829151 | ||
| The cellular production of hydrogen peroxide | Q41880555 | ||
| Altered mitochondrial function in fibroblasts containing MELAS or MERRF mitochondrial DNA mutations. | Q42077715 | ||
| An assay for superoxide dismutase activity in mammalian tissue homogenates | Q45026389 | ||
| The clinical features of mitochondrial myopathy | Q48291336 | ||
| Regional distribution of superoxide dismutase in rat brain during postnatal development. | Q48925325 | ||
| Mitochondrial respiratory chain inhibitors induce apoptosis. | Q52544710 | ||
| Infantile mitochondria encephalomyopathies: report on 4 cases | Q70577941 | ||
| Glucose transport and metabolism in cultured human skin fibroblasts | Q71679569 | ||
| Superoxide dismutases of muscle in mitochondrial encephalomyopathies | Q71758860 | ||
| Effects of 1-methyl-4-phenylpyridinium on isolated rat brain mitochondria: evidence for a primary involvement of energy depletion | Q72069865 | ||
| P433 | issue | 8 | |
| P304 | page(s) | 925-931 | |
| P577 | publication date | 1999-12-01 | |
| P1433 | published in | Journal of Inherited Metabolic Disease | Q6295359 |
| P1476 | title | Mitochondrial respiratory chain defects are not accompanied by an increase in the activities of lactate dehydrogenase or manganese superoxide dismutase in paediatric skeletal muscle biopsies | |
| P478 | volume | 22 |
| Q35088844 | Absence of intracellular ion channels TPC1 and TPC2 leads to mature-onset obesity in male mice, due to impaired lipid availability for thermogenesis in brown adipose tissue. |
| Q28658576 | Autosomal-recessive cerebellar ataxia caused by a novel ADCK3 mutation that elongates the protein: clinical, genetic and biochemical characterisation |
| Q34347182 | Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene |
| Q39318947 | Human neuronal coenzyme Q10 deficiency results in global loss of mitochondrial respiratory chain activity, increased mitochondrial oxidative stress and reversal of ATP synthase activity: implications for pathogenesis and treatment. |
| Q40303782 | Not only insulin stimulates mitochondriogenesis in muscle cells, but mitochondria are also essential for insulin-mediated myogenesis |
| Q37096592 | Nrf2 impacts cellular bioenergetics by controlling substrate availability for mitochondrial respiration. |
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