Pages that link to "Q41244266"
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The following pages link to Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines (Q41244266):
Displaying 50 items.
- Ancient mtDNA genetic variants modulate mtDNA transcription and replication (Q21092461) (← links)
- Mitochondrial dysfunction and mitophagy activation in blood mononuclear cells of fibromyalgia patients: implications in the pathogenesis of the disease (Q21195362) (← links)
- Diabetic cardiomyopathy-associated dysfunction in spatially distinct mitochondrial subpopulations (Q23912644) (← links)
- Late-onset Leigh syndrome in a patient with mitochondrial complex I NDUFS8 mutations (Q24294235) (← links)
- Structural organization of mitochondrial human complex I: role of the ND4 and ND5 mitochondria-encoded subunits and interaction with prohibitin (Q24299240) (← links)
- Mammalian polynucleotide phosphorylase is an intermembrane space RNase that maintains mitochondrial homeostasis (Q24302448) (← links)
- Phosphate-activated glutaminase (GLS2), a p53-inducible regulator of glutamine metabolism and reactive oxygen species (Q24305112) (← links)
- Lon protease preferentially degrades oxidized mitochondrial aconitase by an ATP-stimulated mechanism (Q24305348) (← links)
- Human ind1, an iron-sulfur cluster assembly factor for respiratory complex I (Q24315990) (← links)
- Role of SUV3 helicase in maintaining mitochondrial homeostasis in human cells (Q24320354) (← links)
- Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome (Q24324444) (← links)
- Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 epsilon subunit (Q24324788) (← links)
- Hsp27 as a negative regulator of cytochrome C release (Q24536983) (← links)
- A mutation of beta -actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystonia (Q24546532) (← links)
- Metabolic control analysis in a cellular model of elevated MAO-B: relevance to Parkinson's disease (Q24651159) (← links)
- Sarcalumenin is essential for maintaining cardiac function during endurance exercise training (Q24654268) (← links)
- The NDUFA1 gene product (MWFE protein) is essential for activity of complex I in mammalian mitochondria (Q24675867) (← links)
- Truncated product of the bifunctional DLST gene involved in biogenesis of the respiratory chain (Q24679782) (← links)
- Mitochondrial DNA variation in human radiation and disease (Q26781103) (← links)
- Mitochondrial genetics and obesity: evolutionary adaptation and contemporary disease susceptibility (Q27022800) (← links)
- MAO-B elevation in mouse brain astrocytes results in Parkinson's pathology (Q27301926) (← links)
- Postnatal proteasome inhibition induces neurodegeneration and cognitive deficiencies in adult mice: a new model of neurodevelopment syndrome (Q27311182) (← links)
- Skeletal muscle mitochondrial health and spinal cord injury (Q28074178) (← links)
- Mitochondrial ribosomal RNA (rRNA) methyltransferase family members are positioned to modify nascent rRNA in foci near the mitochondrial DNA nucleoid (Q28116543) (← links)
- Conditional knockdown of hMRS2 results in loss of mitochondrial Mg(2+) uptake and cell death (Q28118613) (← links)
- The ADP/ATP translocator is not essential for the mitochondrial permeability transition pore (Q28241418) (← links)
- Syndromic parkinsonism and dementia associated with OPA1 missense mutations (Q28259640) (← links)
- The enzymatic function of tafazzin (Q28272001) (← links)
- Deletion of skeletal muscle SOCS3 prevents insulin resistance in obesity (Q28274712) (← links)
- A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function (Q28289677) (← links)
- Transmission and prenatal diagnosis of the T9176C mitochondrial DNA mutation (Q28307177) (← links)
- Mitochondrial toxin 3-nitropropionic acid induces cardiac and neurotoxicity differentially in mice (Q28360954) (← links)
- Mitochondrial dysfunction in the type 2 diabetic heart is associated with alterations in spatially distinct mitochondrial proteomes (Q28383016) (← links)
- Transgenic overexpression of mitofilin attenuates diabetes mellitus-associated cardiac and mitochondria dysfunction (Q28386173) (← links)
- Functional deficiencies of subsarcolemmal mitochondria in the type 2 diabetic human heart (Q28389334) (← links)
- The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity (Q28392028) (← links)
- Reversal of mitochondrial proteomic loss in Type 1 diabetic heart with overexpression of phospholipid hydroperoxide glutathione peroxidase (Q28396972) (← links)
- Suppression of oxidative stress by resveratrol after isometric contractions in gastrocnemius muscles of aged mice (Q28397026) (← links)
- Heterozygous mutation of Drosophila Opa1 causes the development of multiple organ abnormalities in an age-dependent and organ-specific manner (Q28476042) (← links)
- Metabolic adaptation to chronic inhibition of mitochondrial protein synthesis in acute myeloid leukemia cells (Q28487801) (← links)
- Mitochondrial disease in superoxide dismutase 2 mutant mice (Q28513450) (← links)
- Inhibition of cathepsin B by E-64 induces oxidative stress and apoptosis in filarial parasite (Q28541533) (← links)
- Mitochondrial modulation by Epigallocatechin 3-Gallate ameliorates cisplatin induced renal injury through decreasing oxidative/nitrative stress, inflammation and NF-kB in mice (Q28546437) (← links)
- Deep Sequencing Reveals Novel Genetic Variants in Children with Acute Liver Failure and Tissue Evidence of Impaired Energy Metabolism (Q28553351) (← links)
- Mitochondrial Probe Methyltriphenylphosphonium (TPMP) Inhibits the Krebs Cycle Enzyme 2-Oxoglutarate Dehydrogenase (Q28553591) (← links)
- Selective binding of nuclear alpha-synuclein to the PGC1alpha promoter under conditions of oxidative stress may contribute to losses in mitochondrial function: implications for Parkinson's disease (Q28576367) (← links)
- p53 and tumor necrosis factor alpha regulate the expression of a mitochondrial chloride channel protein (Q28585207) (← links)
- p32/gC1qR is indispensable for fetal development and mitochondrial translation: importance of its RNA-binding ability (Q28587023) (← links)
- Increased mitochondrial oxidative stress in the Sod2 (+/-) mouse results in the age-related decline of mitochondrial function culminating in increased apoptosis (Q28587044) (← links)
- Mitochondrial basis for immune deficiency. Evidence from purine nucleoside phosphorylase-deficient mice (Q28590225) (← links)