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©
Terkko 2005-2021
Ku70 modulation alleviates murine allergic asthma features and restores mitochondrial function in lungs
Mitochondrion
5 hours
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The nuclear factor kappa B (NF-κB) signaling pathway is involved in ammonia-induced mitochondrial dysfunction
Mitochondrion
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Mitochondrial calcium in command of juggling myriads of cellular functions
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Altered mitochondrial calcium handling and cell death by necroptosis: An emerging paradigm
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Alterations in inter-organelle crosstalk and Ca2+ signaling through mitochondria during proteotoxic stresses
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Mitochondrial dysfunction as a critical event in the pathophysiology of bipolar disorder
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Molecular machinery regulating mitochondrial calcium levels: The nuts and bolts of mitochondrial calcium dynamics
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A mitochondrial myopathy-associated tRNASer(UCN) 7453G>A mutation alters tRNA metabolism and mitochondrial function
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Evaluation of anticancer role of a novel ruthenium(II)-based compound compared with NAMI-A and cisplatin in impairing mitochondrial functionality and promoting oxidative stress in triple negative breast cancer models
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Mitohormesis; Potential implications in neurodegenerative diseases
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Stem cell plasticity and regenerative potential regulation through Ca2+-mediated mitochondrial nuclear crosstalk
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Mitochondrial Genetic Effect on Atrial Fibrillation: A Case-Control Study
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Homoplasmic deleterious MT-ATP6/8 mutations in adult patients
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Mental health and health related quality of life in mitochondrial POLG disease
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Detection of mitochondria-pertinent components in exosomes
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Placental mitochondrial DNA mutations and copy numbers in intrauterine growth restricted (IUGR) pregnancy
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ATM mediated-p53 signaling pathway forms a novel axis for senescence control
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Associations of mitochondrial DNA copy number and deletion rate with early pregnancy loss
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The effect of short-term methionine restriction on hydrogen peroxide metabolism in Fischer-344 rat skeletal muscle mitochondria
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Distinguishing Mitochondrial DNA and NUMT Sequences Amplified with the Precision ID mtDNA Whole Genome Panel
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Complex I deficiency, due to NDUFAF4 mutations, causes severe mitochondrial dysfunction and is associated to early death and dysmorphia
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The mitochondrial DNA variant m.9032T>C in MT-ATP6 encoding p.(Leu169Pro) causes a complex mitochondrial neurological syndrome
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Association of mitochondrial DNA content and displacement loop region sequence variations with cancer-related fatigue in breast cancer survivors receiving chemotherapy
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Altered spontaneous brain activity at attack and remission stages in patients with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS): Beyond stroke-like lesions
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Aminoacyl-tRNA synthetases and translational quality control in plant mitochondria
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Mitochondria and microbiota dysfunction in COVID-19 pathogenesis
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Altered mitochondrial proteome and functional dynamics in patients with rheumatoid arthritis
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Effects of dietary iron restriction on kidney mitochondria function and oxidative stress in streptozotocin-diabetic rats
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A novel m.11406T>A mutation in mitochondrial ND4 gene causes MELAS Syndrome
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Analysis of variants in mitochondrial genome and their putative pathogenicity in Tuberculosis patients from Mizoram, North east India
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Discovery of ubiquinone (coenzyme Q) and an overview of function
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