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- ATP Synthase Diseases of Mitochondrial Genetic Origin Alain Dautant, Thomas Meier, Alexander Hahn, Deborah Tribouillard-Tanvier, Jean-Paul Di Rago, Roza Kucharczyk
- Altered Expression of Mitoferrin and Frataxin, Larger Labile Iron Pool and Greater Mitochondrial DNA Damage in the Skeletal Muscle of Older Adults
- Terpestacin Inhibits Tumor Angiogenesis by Targeting UQCRB of Mitochondrial Complex III and Suppressing Hypoxia-Induced Reactive
- Mitochondrial DNA Genome Sequencing and SNP Assay Development for Increased Power of Discrimination
- Genes Feel the Heat
- Import of Non-Coding Rnas Into Human Mitochondria: a Critical Review and Emerging Approaches
- Mitochondrial DNA
- Mitochondrial UQCRB As a New Molecular Prognostic Biomarker of Human Colorectal Cancer
- Mitochondrial Complex III Deficiency
- Engineering Genetic Systems for Treating Mitochondrial Diseases
- Mitochondrial DNA (Mtdna) Test Requisition
- Mitochondrial DNA in Human Identification: a Review
- Pyruvate Dehydrogenase Complex - Correlation Between Structure and Function
- Neuropathy, Ataxia, and Retinitis Pigmentosa
- Role of Monoamine Oxidase a (MAO-A) in Cardiac Aging
- Mitochondria, Oxidative Stress and the Kynurenine System, with a Focus on Ageing and Neuroprotection
- The Genetic Evidence of Burn-Induced Cardiac Mitochondrial Metabolism Dysfunction
- The Generation of Mitochondrial DNA Large-Scale Deletions in Human Cells
- Mitochondrial Pyruvate Dehydrogenase Phosphatase 1 Regulates the Early Differentiation of Cardiomyocytes from Mouse Embryonic Stem Cells
- Redox Biology Monoamine Oxidase-A Promotes Protective Autophagy In
- The Involvement of the Kynurenine Pathway in Parkinson’S Disease in Vitro Models
- Adult Onset Limb-Girdle Type Mitochondrial Myopathy with a Mitochondrial DNA Np8291 A-To-G Substitution
- Ammonia Inhibits Energy Metabolism in Astrocytes in a Rapid And
- Mitochondrial DNA and Ancestry Genomic DNA Is Found in the Cell Nucleus and Is Passed Down Equally from Both Parents
- Mitochondrial DNA Depletion by Ethidium Bromide Decreases Neuronal Mitochondrial Creatine Kinase: Implications for Striatal Energy Metabolism
- Pathogenic Mitochondria DNA Mutations: Current Detection Tools and Interventions
- Mitochondrial DNA
- Monoamine Oxidase-A Promotes Protective Autophagy in Human SH-SY5Y Neuroblastoma Cells Through Bcl-2 Phosphorylation T ⁎ Aslihan Ugun-Kluseka, , Theodosis S
- The KMO Allele Encoding Arg452 Is Associated with Psychotic Features in Bipolar Disorder Type 1, and with Increased CSF KYNA Level and Reduced KMO Expression
- Recurrent Heteroplasmy for the MT-ATP6 P.Ser148asn
- Evidence for the Role of Mitochondrial DNA Release in the Inflammatory Response in Neurological Disorders
- Mitochondrial Oxodicarboxylate Carrier Deficiency Is Associated with Mitochondrial DNA Depletion and Spinal Muscular Atrophy–Like Disease
- The Similarities Between Human Mitochondria and Bacteria in the Context of Structure, Genome, and Base Excision Repair System
- Role of Kynurenine Pathway in Oxidative Stress During Neurodegenerative Disorders
- Mitochondrial DNA Sequencing Reveals Association of Variants And
- Mitochondrial Myopathy Presenting As Rhabdomyolysis CASE REPORT