Mitochondrion is a definitive, high profile, peer-reviewed international research journal. The scope of Mitochondrion is broad, reporting on basic science of mitochondria from all organisms and from basic research to pathology and clinical aspects of mitochondrial diseases. The journal welcomes original contributions from investigators working in diverse sub-disciplines such as evolution, biophysics, biochemistry, molecular and cell biology, genetics, pharmacology, toxicology, forensic science, programmed cell death, aging, cancer and clinical features of mitochondrial diseases.
线粒体是一个权威的，高姿态，同行评议的国际研究杂志。线粒体的研究范围很广，涵盖了所有生物体的线粒体基础科学，从基础研究到线粒体疾病的病理学和临床方面。该杂志欢迎来自不同子学科的研究人员的原创贡献，如进化、生物物理学、生物化学、分子和细胞生物学、遗传学、药理学、毒理学、法医学、程序性细胞死亡、衰老、癌症和线粒体疾病的临床特征。
Mitochondrial β-oxidation of saturated fatty acids in humans.
来源期刊：MitochondrionDOI：10.1016/j.mito.2018.02.009
Mitochondrial dysfunction in neurodegenerative diseases and drug targets via apoptotic signaling.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.07.003
Withaferin A-mediated apoptosis in breast cancer cells is associated with alterations in mitochondrial dynamics.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.01.003
Effects of air pollution on mitochondrial function, mitochondrial DNA methylation, and mitochondrial peptide expression.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.04.001
Forms of extracellular mitochondria and their impact in health.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.02.002
Modular Biogenesis of Mitochondrial Respiratory Complexes.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.10.008
Peroxynitrite nitrates adenine nucleotide translocase and voltage-dependent anion channel 1 and alters their interactions and association with hexokinase II in mitochondria.
来源期刊：MitochondrionDOI：10.1016/j.mito.2018.10.002
Exercise-induced reductions in mitochondrial ADP sensitivity contribute to the induction of gene expression and mitochondrial biogenesis through enhanced mitochondrial H2O2 emission.
来源期刊：MitochondrionDOI：10.1016/j.mito.2018.03.003
Impact of mitochondrial DNA copy number and displacement loop alterations on polycystic ovary syndrome risk in south Indian women.
来源期刊：MitochondrionDOI：10.1016/j.mito.2017.12.010
Multichromosomal structure of the onion mitochondrial genome and a transcript analysis.
来源期刊：MitochondrionDOI：10.1016/j.mito.2018.05.001
Development of a triplex mtDNA qPCR assay to assess quantification, degradation, inhibition, and amplification target copy numbers.
来源期刊：MitochondrionDOI：10.1016/j.mito.2018.09.007
Alterations of oxygen consumption and extracellular acidification rates by glutamine in PBMCs of SLE patients.
来源期刊：MitochondrionDOI：10.1016/j.mito.2018.01.002
Mitochondrial dysfunction caused by m.2336T>C mutation with hypertrophic cardiomyopathy in cybrid cell lines.
来源期刊：MitochondrionDOI：10.1016/j.mito.2018.08.005
Mitochondrial-associated protein biomarkers in patients with attention-deficit/hyperactivity disorder.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.07.007
Tracing the maternal origin of the common wall lizard (Podarcis muralis) on the northern range margin in Central Europe.
来源期刊：MitochondrionDOI：10.1016/j.mito.2018.04.006
Iba57p participates in maturation of a [2Fe-2S]-cluster Rieske protein and in formation of supercomplexes III/IV of Saccharomyces cerevisiae electron transport chain.
来源期刊：MitochondrionDOI：10.1016/j.mito.2018.01.003
Sensitivity of mitochondrial DNA heteroplasmy detection using Next Generation Sequencing.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.10.006
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.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.04.006
PPARδ modulation rescues mitochondrial fatty acid oxidation defects in the mdx model of muscular dystrophy.
来源期刊：MitochondrionDOI：10.1016/j.mito.2018.02.006
Genomic and transcriptomic characterization of the mitochondrial-rich oncocytic phenotype on a thyroid carcinoma background.
来源期刊：MitochondrionDOI：10.1016/j.mito.2018.04.001
Mitonuclear gene X environment effects on lifespan and health: How common, how big?
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.06.009
Mitochondrial mRNA Fragments are Circularized in a Human HEK Cell Line.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.11.002
Growth and Differentiation Factor 15 as a biomarker for mitochondrial myopathy.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.10.005
Mitochondria-targeted quinones suppress the generation of reactive oxygen species, programmed cell death and senescence in plants.
来源期刊：MitochondrionDOI：10.1016/j.mito.2018.04.008
Ironing the mitochondria: Relevance to its dynamics.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.09.007
Whole mitochondria genome mutational spectrum in occupationally exposed lead subjects.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.04.009
Extracellular matrix/mitochondria pathway: a novel potential target for sarcopenia.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.10.007
Three rare pathogenic mtDNA substitutions in LHON patients with low heteroplasmy.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.10.002
Endoplasmic reticulum stress induced apoptosis and caspase activation is mediated through mitochondria during megakaryocyte differentiation.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.10.009
Targeted next generation sequencing identifies novel pathogenic variants and provides molecular diagnoses in a cohort of pediatric and adult patients with unexplained mitochondrial dysfunction.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.02.006
A proteomic analysis of Caenorhabditis elegans mitochondria during bacterial infection.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.03.002
Non-invasive versus ex vivo measurement of mitochondrial function in an endotoxemia model in rat: toward monitoring of mitochondrial therapy.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.11.003
Molecular dynamics simulations on apo ADP/ATP carrier shed new lights on the featured motif of the mitochondrial carriers.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.05.006
Mitochondrial oxidative phosphorylation capacity of cryopreserved cells.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.04.011
Mitochondrial chaperone, TRAP1 as a potential pharmacological target to combat cancer metabolism.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.09.011
A mitochondrial DNA D loop insertion detected almost exclusively in non-replicating tissues with maternal inheritance across three generations.
来源期刊：MitochondrionDOI：10.1016/j.mito.2018.08.002
Myasthenia gravis like symptoms associated with rare mitochondrial mutation (m.5728T>C).
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.04.003
Cetylpyridinium chloride is a potent AMP-activated kinase (AMPK) inducer and has therapeutic potential in cancer.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.09.009
A case report on a novel MT-ATP6 gene variation in atypical mitochondrial Leigh syndrome associated with bilateral basal ganglia calcifications.
来源期刊：MitochondrionDOI：10.1016/j.mito.2018.06.005
Intramitochondrial transfer and engineering of mammalian mitochondrial genomes in yeast.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.03.006
A zebrafish model to study small-fiber neuropathy reveals a potential role for GDAP1.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.01.002
Leigh syndrome caused by mitochondrial DNA-maintenance defects revealed by whole exome sequencing.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.06.008
Prenatal onset of mitochondrial disease is associated with sideroflexin 4 deficiency.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.04.012
A novel pathogenic m.4412G>A MT-TM mitochondrial DNA variant associated with childhood-onset seizures, myopathy and bilateral basal ganglia changes
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.04.007
Gene therapy for the mitochondrial genome: Purging mutations, pacifying ailments.
来源期刊：MitochondrionDOI：10.1016/j.mito.2018.06.002
Mitochondrial haplotypes are not associated with mice selectively bred for high voluntary wheel running.
来源期刊：MitochondrionDOI：10.1016/j.mito.2018.04.002
Complete elimination of a pathogenic homoplasmic mtDNA mutation in one generation.
来源期刊：MitochondrionDOI：10.1016/j.mito.2018.01.010
Germline knockdown of spargel (PGC-1) produces embryonic lethality in Drosophila.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.08.006
Pyridine nucleotide-disulphide oxidoreductase domain 2 (PYROXD2): Role in mitochondrial function.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.05.007
Role of ectopically expressed mtDNA encoded cytochrome c oxidase subunit I (MT-COI) in tumorigenesis.
来源期刊：MitochondrionDOI：10.1016/j.mito.2019.07.002
