MITOCHONDRION

Effects of air pollution on mitochondrial function, mitochondrial DNA methylation, and mitochondrial peptide expression.

Forms of extracellular mitochondria and their impact in health.

Modular Biogenesis of Mitochondrial Respiratory Complexes.

Peroxynitrite nitrates adenine nucleotide translocase and voltage-dependent anion channel 1 and alters their interactions and association with hexokinase II in mitochondria.

Exercise-induced reductions in mitochondrial ADP sensitivity contribute to the induction of gene expression and mitochondrial biogenesis through enhanced mitochondrial H2O2 emission.

Impact of mitochondrial DNA copy number and displacement loop alterations on polycystic ovary syndrome risk in south Indian women.

Multichromosomal structure of the onion mitochondrial genome and a transcript analysis.

Development of a triplex mtDNA qPCR assay to assess quantification, degradation, inhibition, and amplification target copy numbers.

Alterations of oxygen consumption and extracellular acidification rates by glutamine in PBMCs of SLE patients.

Mitochondrial dysfunction caused by m.2336T>C mutation with hypertrophic cardiomyopathy in cybrid cell lines.

Mitochondrial-associated protein biomarkers in patients with attention-deficit/hyperactivity disorder.

Tracing the maternal origin of the common wall lizard (Podarcis muralis) on the northern range margin in Central Europe.

Iba57p participates in maturation of a [2Fe-2S]-cluster Rieske protein and in formation of supercomplexes III/IV of Saccharomyces cerevisiae electron transport chain.

Sensitivity of mitochondrial DNA heteroplasmy detection using Next Generation Sequencing.

Leukocyte mitochondrial DNA copy number as a potential biomarker indicating poor outcome in biliary atresia and its association with oxidative DNA damage and telomere length.

PPARδ modulation rescues mitochondrial fatty acid oxidation defects in the mdx model of muscular dystrophy.

Genomic and transcriptomic characterization of the mitochondrial-rich oncocytic phenotype on a thyroid carcinoma background.

Mitonuclear gene X environment effects on lifespan and health: How common, how big?

Mitochondrial mRNA Fragments are Circularized in a Human HEK Cell Line.

Growth and Differentiation Factor 15 as a biomarker for mitochondrial myopathy.

Mitochondria-targeted quinones suppress the generation of reactive oxygen species, programmed cell death and senescence in plants.

Ironing the mitochondria: Relevance to its dynamics.

Whole mitochondria genome mutational spectrum in occupationally exposed lead subjects.

Extracellular matrix/mitochondria pathway: a novel potential target for sarcopenia.

Three rare pathogenic mtDNA substitutions in LHON patients with low heteroplasmy.

Endoplasmic reticulum stress induced apoptosis and caspase activation is mediated through mitochondria during megakaryocyte differentiation.

Targeted next generation sequencing identifies novel pathogenic variants and provides molecular diagnoses in a cohort of pediatric and adult patients with unexplained mitochondrial dysfunction.

A proteomic analysis of Caenorhabditis elegans mitochondria during bacterial infection.

Non-invasive versus ex vivo measurement of mitochondrial function in an endotoxemia model in rat: toward monitoring of mitochondrial therapy.

Molecular dynamics simulations on apo ADP/ATP carrier shed new lights on the featured motif of the mitochondrial carriers.

Mitochondrial oxidative phosphorylation capacity of cryopreserved cells.

Mitochondrial chaperone, TRAP1 as a potential pharmacological target to combat cancer metabolism.

A mitochondrial DNA D loop insertion detected almost exclusively in non-replicating tissues with maternal inheritance across three generations.

Myasthenia gravis like symptoms associated with rare mitochondrial mutation (m.5728T>C).

Cetylpyridinium chloride is a potent AMP-activated kinase (AMPK) inducer and has therapeutic potential in cancer.

A case report on a novel MT-ATP6 gene variation in atypical mitochondrial Leigh syndrome associated with bilateral basal ganglia calcifications.

Intramitochondrial transfer and engineering of mammalian mitochondrial genomes in yeast.

A zebrafish model to study small-fiber neuropathy reveals a potential role for GDAP1.

Leigh syndrome caused by mitochondrial DNA-maintenance defects revealed by whole exome sequencing.

Prenatal onset of mitochondrial disease is associated with sideroflexin 4 deficiency.

A novel pathogenic m.4412G>A MT-TM mitochondrial DNA variant associated with childhood-onset seizures, myopathy and bilateral basal ganglia changes

Gene therapy for the mitochondrial genome: Purging mutations, pacifying ailments.

Mitochondrial haplotypes are not associated with mice selectively bred for high voluntary wheel running.

Complete elimination of a pathogenic homoplasmic mtDNA mutation in one generation.

Germline knockdown of spargel (PGC-1) produces embryonic lethality in Drosophila.

Pyridine nucleotide-disulphide oxidoreductase domain 2 (PYROXD2): Role in mitochondrial function.

Role of ectopically expressed mtDNA encoded cytochrome c oxidase subunit I (MT-COI) in tumorigenesis.