Pages that link to "Q26769015"

The following pages link to Mitochondrial cytochrome c oxidase deficiency (Q26769015):

Displaying 23 items.

• The effects of indoor and outdoor temperature on metabolic rate and adipose tissue - the Mississippi perspective on the obesity epidemic (Q31095165) (← links)
• Tissue- and Condition-Specific Isoforms of Mammalian Cytochrome c Oxidase Subunits: From Function to Human Disease (Q33737679) (← links)
• The genetics and pathology of mitochondrial disease. (Q37560946) (← links)
• Respiratory chain supercomplexes: Structures, function and biogenesis. (Q38661650) (← links)
• A CMC1-knockout reveals translation-independent control of human mitochondrial complex IV biogenesis. (Q38721574) (← links)
• COA7 (C1orf163/RESA1) mutations associated with mitochondrial leukoencephalopathy and cytochrome c oxidase deficiency (Q42328121) (← links)
• Mutation in the COX4I1 gene is associated with short stature, poor weight gain and increased chromosomal breaks, simulating Fanconi anemia (Q46327397) (← links)
• New insights into mitogenomic phylogeny and copy number in eight indigenous sheep populations based on the ATP synthase and cytochrome c oxidase genes (Q47397136) (← links)
• Cytochrome c oxidase deficiency, oxidative stress, possible antioxidant therapy and link to nuclear DNA damage. (Q49357584) (← links)
• RNA-Seq Analysis of Islets to Characterise the Dedifferentiation in Type 2 Diabetes Model Mice db/db (Q51739972) (← links)
• The Complexity of Mitochondrial Complex IV: An Update of Cytochrome c Oxidase Biogenesis in Plants. (Q51745738) (← links)
• Mitochondrial complex IV deficiency caused by a novel frameshift variant in MT-CO2 associated with myopathy and perturbed acylcarnitine profile (Q57470919) (← links)
• APOPT1/COA8 assists COX assembly and is oppositely regulated by UPS and ROS (Q60954715) (← links)
• Mitochondrial Genetic Disorders: Cell Signaling and Pharmacological Therapies. (Q64943955) (← links)
• Phosphorylated Glycogen Synthase Kinase-3β (GSK-3β) Improves Cognition in Rats with Diabetes-Associated Cognitive Decline. (Q64964666) (← links)
• Structural and functional characterization of the mitochondrial complex IV assembly factor Coa6 (Q90083302) (← links)
• Pathogenic variants in SQOR encoding sulfide:quinone oxidoreductase are a potentially treatable cause of Leigh disease (Q90237465) (← links)
• Metabolic Alterations in Inherited Cardiomyopathies (Q92012621) (← links)
• Autosomal dominant transmission of transient neonatal lactic acidosis: a case report (Q92087651) (← links)
• A Novel Pathogenic Variant in MT-CO2 Causes an Isolated Mitochondrial Complex IV Deficiency and Late-Onset Cerebellar Ataxia (Q92543630) (← links)
• COX deficiency and leukoencephalopathy due to a novel homozygous APOPT1/COA8 mutation (Q97425228) (← links)
• SURF1 related Leigh syndrome: Clinical and molecular findings of 16 patients from Turkey (Q101145232) (← links)
• Systematic review and meta-analysis on the role of mitochondrial cytochrome c oxidase in Alzheimer's disease (Q103795241) (← links)