Pages that link to "Q68660930"
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The following pages link to Oxidative phosphorylation in mitochondria isolated from human fibroblasts (Q68660930):
Displaying 18 items.
- Altered phosphorylation state of branched-chain 2-oxo acid dehydrogenase in a branched-chain acyltransferase deficient human fibroblast cell line (Q28286648) (← links)
- Demonstration of a specific mitochondrial isovaleryl-CoA dehydrogenase deficiency in fibroblasts from patients with isovaleric acidemia (Q28615562) (← links)
- Respiratory chain defects in the mitochondria of cultured skin fibroblasts from three patients with lacticacidemia (Q34577359) (← links)
- The French and North American phenotypes of pyruvate carboxylase deficiency, correlation with biotin containing protein by 3H-biotin incorporation, 35S-streptavidin labeling, and Northern blotting with a cloned cDNA probe (Q35198796) (← links)
- Abnormal kinetic behavior of cytochrome oxidase in a case of Leigh disease (Q35199469) (← links)
- Oxidative phosphorylation in rat oral mucosal mitochondria (Q40118629) (← links)
- Oligomycin induces a decrease in the cellular content of a pathogenic mutation in the human mitochondrial ATPase 6 gene. (Q40964939) (← links)
- Isolation and characterization of mitochondria from human B lymphoblastoid cell lines (Q41613950) (← links)
- Characterization of the respiratory activity of mitochondria isolated from an insect cell line CP-1268 Laspeyresia pomonella (Q42076582) (← links)
- Fatal combined defects in mitochondrial multienzyme complexes in two siblings (Q42452012) (← links)
- Clinical presentation of mitochondrial respiratory chain defects in NADH-coenzyme Q reductase and cytochrome oxidase: clues to pathogenesis of Leigh disease (Q43499491) (← links)
- Oxidative phosphorylation by chondrocyte mitochondria (Q45139457) (← links)
- Immunochemical study in three patients with cytochrome c oxidase deficiency presenting Leigh's encephalomyelopathy (Q48259705) (← links)
- Cytochrome C oxidase deficiency in two siblings with leigh encephalomyelopathy (Q48700715) (← links)
- Two siblings with cytochromec oxidase deficiency (Q48839592) (← links)
- Detection of respiratory chain dysfunction by measuring lactate and pyruvate production in cultured fibroblasts (Q68484617) (← links)
- Comparative biochemical studies in fibroblasts from patients with different forms of Leigh syndrome (Q71587092) (← links)
- Comparative biochemical studies of ATPases in cells from patients with the T8993G or T8993C mitochondrial DNA mutations (Q77740217) (← links)