| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/TP.2013.68 |
| P2888 | exact match | https://scigraph.springernature.com/pub.10.1038/tp.2013.68 |
| P932 | PMC publication ID | 3784762 |
| P698 | PubMed publication ID | 24002085 |
| P5875 | ResearchGate publication ID | 256424969 |
| P2093 | author name string | F Gu | |
| K Kaur | |||
| A Chauhan | |||
| W T Brown | |||
| J Wegiel | |||
| V Chauhan | |||
| G LaFauci | |||
| P2860 | cites work | Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis | Q24630557 |
| Strong association of de novo copy number mutations with autism | Q24633543 | ||
| Global variation in copy number in the human genome | Q24658083 | ||
| Detection of large-scale variation in the human genome | Q28131803 | ||
| Association between microdeletion and microduplication at 16p11.2 and autism | Q28264205 | ||
| Mitochondrial disease in autism spectrum disorder patients: a cohort analysis | Q28474112 | ||
| Complex III releases superoxide to both sides of the inner mitochondrial membrane | Q28509539 | ||
| Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism | Q29013643 | ||
| Mitochondrial free radical generation, oxidative stress, and aging | Q29614202 | ||
| Mitochondrial DNA damage is more extensive and persists longer than nuclear DNA damage in human cells following oxidative stress | Q29619552 | ||
| The reduction of NADH ubiquinone oxidoreductase 24- and 75-kDa subunits in brains of patients with Down syndrome and Alzheimer's disease | Q30991755 | ||
| Magnetic resonance spectroscopy in affective disorders | Q32062252 | ||
| Respiratory chain complex I deficiency: an underdiagnosed energy generation disorder | Q33600939 | ||
| Mitochondrial oxygen radical generation and leak: sites of production in states 4 and 3, organ specificity, and relation to aging and longevity | Q33832703 | ||
| Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders | Q33874840 | ||
| MitoProteome: mitochondrial protein sequence database and annotation system | Q33974667 | ||
| Mitochondrial complex I activity and oxidative damage to mitochondrial proteins in the prefrontal cortex of patients with bipolar disorder | Q34108449 | ||
| The mitochondrial production of reactive oxygen species: mechanisms and implications in human pathology | Q34109999 | ||
| Nutritional and metabolic status of children with autism vs. neurotypical children, and the association with autism severity | Q35102732 | ||
| Altered dopamine metabolism and increased vulnerability to MPTP in mice with partial deficiency of mitochondrial complex I in dopamine neurons | Q35750220 | ||
| Mitochondrial biogenesis and mitochondrial DNA maintenance of mammalian cells under oxidative stress. | Q36032328 | ||
| Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways | Q36083120 | ||
| Mitochondrial and ion channel gene alterations in autism. | Q36178457 | ||
| Association testing of copy number variants in schizophrenia and autism spectrum disorders | Q36217805 | ||
| Analysis of copy number variations in brain DNA from patients with schizophrenia and other psychiatric disorders | Q36275712 | ||
| Mitochondrial complex I: structure, function and pathology | Q36534792 | ||
| Supramolecular structure of the mitochondrial oxidative phosphorylation system | Q36652816 | ||
| Brain region-specific deficit in mitochondrial electron transport chain complexes in children with autism | Q36820898 | ||
| Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism | Q37029453 | ||
| Support for the involvement of large copy number variants in the pathogenesis of schizophrenia | Q37147142 | ||
| The role of abnormal mitochondrial dynamics in the pathogenesis of Alzheimer's disease | Q37459062 | ||
| Mitochondrial dysfunction in autism | Q37558748 | ||
| High frequencies of de novo CNVs in bipolar disorder and schizophrenia | Q37578876 | ||
| Brain mitochondria as a primary target in the development of treatment strategies for Alzheimer disease | Q37585755 | ||
| Fever plus mitochondrial disease could be risk factors for autistic regression | Q37601811 | ||
| Mitochondrial dysfunction in autism spectrum disorders: cause or effect? | Q37742216 | ||
| Mitochondria dysfunction and neurodegenerative disorders: cause or consequence | Q37750253 | ||
| New insights into the role of mitochondrial dysfunction and protein aggregation in Parkinson's disease | Q37776882 | ||
| Autism and mitochondrial disease | Q37785513 | ||
| Implications of gene copy-number variation in health and diseases. | Q37940158 | ||
| Genetic architecture in autism spectrum disorder | Q37998609 | ||
| Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology? | Q38010589 | ||
| Mitochondrial respiratory chain dysfunction: implications in neurodegeneration. | Q38010826 | ||
| Mitochondrial gene expression in mammalian striated muscle. Evidence that variation in gene dosage is the major regulatory event | Q41472476 | ||
| Mitochondrial DNA copy number is proportional to total cell DNA under a variety of growth conditions | Q41721947 | ||
| Evidence for a mitochondrial oxidative phosphorylation defect in brains from patients with schizophrenia | Q42501952 | ||
| Autism associated to a deficiency of complexes III and IV of the mitochondrial respiratory chain. | Q42751992 | ||
| Mitochondrial DNA and respiratory chain function in spinal cords of ALS patients | Q43883813 | ||
| Analysis of the subunit composition of complex I from bovine heart mitochondria | Q44367201 | ||
| Oxidative stress-related alteration of the copy number of mitochondrial DNA in human leukocytes | Q44749865 | ||
| Oxidative stress in autism: increased lipid peroxidation and reduced serum levels of ceruloplasmin and transferrin--the antioxidant proteins | Q45055960 | ||
| Mitochondrial enzymes in schizophrenia | Q45085060 | ||
| Mitochondrial dysfunction in autism spectrum disorders: a population-based study. | Q45288693 | ||
| Mitochondrial defect in Huntington's disease caudate nucleus | Q45291734 | ||
| Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder | Q46504843 | ||
| Increased excretion of a lipid peroxidation biomarker in autism. | Q46635423 | ||
| Impaired synthesis and antioxidant defense of glutathione in the cerebellum of autistic subjects: alterations in the activities and protein expression of glutathione-related enzymes | Q47919924 | ||
| Evidence of altered energy metabolism in autistic children | Q48173034 | ||
| A preliminary 31P MRS study of autism: evidence for undersynthesis and increased degradation of brain membranes | Q48273298 | ||
| Brain region-specific glutathione redox imbalance in autism. | Q48552164 | ||
| Decreased levels of complex III core protein 1 and complex V beta chain in brains from patients with Alzheimer's disease and Down syndrome. | Q49132544 | ||
| Brain region-specific changes in oxidative stress and neurotrophin levels in autism spectrum disorders (ASD). | Q50301766 | ||
| Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: no association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene. | Q50302132 | ||
| Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization. | Q50308083 | ||
| Mitochondrial DNA abnormalities and autistic spectrum disorders. | Q50342292 | ||
| A simplified model for mitochondrial ATP production. | Q51934236 | ||
| Decreased cytochrome-c oxidase activity and lack of age-related accumulation of mitochondrial DNA deletions in the brains of schizophrenics. | Q53210206 | ||
| Mitochondrial Dysfunction in Parkinson's Disease | Q61718213 | ||
| Mitochondrial dysfunction and psychiatric disorders | Q79774804 | ||
| De novo CNVs in bipolar disorder: recurrent themes or new directions? | Q83129366 | ||
| Mitochondrial complex I deficiency and ATP/ADP ratio in lymphocytes of amyotrophic lateral sclerosis patients | Q83748135 | ||
| Oxidative stress in autism | Q83965328 | ||
| P921 | main subject | mitochondrion | Q39572 |
| mitochondrial DNA | Q27075 | ||
| autism | Q38404 | ||
| P304 | page(s) | e299 | |
| P577 | publication date | 2013-09-03 | |
| P1433 | published in | Translational Psychiatry | Q15716636 |
| P1476 | title | Alterations in mitochondrial DNA copy number and the activities of electron transport chain complexes and pyruvate dehydrogenase in the frontal cortex from subjects with autism | |
| P478 | volume | 3 |
| Q64082659 | A Pipeline for Faecal Host DNA Analysis by Absolute Quantification of LINE-1 and Mitochondrial Genomic Elements Using ddPCR |
| Q90277751 | Alterations of Mitochondrial Biology in the Oral Mucosa of Chilean Children with Autism Spectrum Disorder (ASD) |
| Q47558706 | An Energetic View of Stress: Focus on Mitochondria |
| Q37433527 | Attention deficit-hyperactivity disorder suffers from mitochondrial dysfunction |
| Q39825160 | CHRONICITY OF DEPRESSION AND MOLECULAR MARKERS IN A LARGE SAMPLE OF HAN CHINESE WOMEN. |
| Q57922552 | Clinical and Molecular Characteristics of Mitochondrial Dysfunction in Autism Spectrum Disorder |
| Q57792524 | Diagnostic and Severity-Tracking Biomarkers for Autism Spectrum Disorder |
| Q50313509 | Difference in mitochondrial DNA copy number in peripheral blood cells between probands with autism spectrum disorders and their unaffected siblings. |
| Q40911590 | Dysferlinopathy: mitochondrial abnormalities in human skeletal muscle |
| Q28066841 | Dysregulated mitochondrial and chloroplast bioenergetics from a translational medical perspective (Review) |
| Q35200891 | Elevated mitochondrial DNA copy number in peripheral blood cells is associated with childhood autism |
| Q38743021 | Epigenetic Treatment of Neuropsychiatric Disorders: Autism and Schizophrenia. |
| Q38666500 | Estimating relative mitochondrial DNA copy number using high throughput sequencing data. |
| Q22241227 | Evidence linking oxidative stress, mitochondrial dysfunction, and inflammation in the brain of individuals with autism |
| Q39384617 | Evidence of Mitochondrial Dysfunction in Autism: Biochemical Links, Genetic-Based Associations, and Non-Energy-Related Mechanisms. |
| Q99402612 | Higher Lactate Level and Lactate-to-Pyruvate Ratio in Autism Spectrum Disorder |
| Q47148010 | Hyperoside alleviates adriamycin-induced podocyte injury via inhibiting mitochondrial fission |
| Q34127735 | Keratoconus is associated with increased copy number of mitochondrial DNA. |
| Q37587055 | Liver Mitochondrial DNA Copy Number and Deletion Levels May Contribute to Nonalcoholic Fatty Liver Disease Susceptibility |
| Q40668798 | Loss of pdr-1/parkin influences Mn homeostasis through altered ferroportin expression in C. elegans |
| Q37534734 | Low-Dose Methylmercury-Induced Genes Regulate Mitochondrial Biogenesis via miR-25 in Immortalized Human Embryonic Neural Progenitor Cells |
| Q39032450 | Mitochondrial Dysfunction in Autism Spectrum Disorders |
| Q36380931 | Mitochondrial Superoxide Contributes to Hippocampal Synaptic Dysfunction and Memory Deficits in Angelman Syndrome Model Mice |
| Q49843158 | Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion. |
| Q30846620 | Modeling environmental risk factors of autism in mice induces IBD-related gut microbial dysbiosis and hyperserotonemia |
| Q48284566 | Monoamine oxidase-A and B activities in the cerebellum and frontal cortex of children and young adults with autism. |
| Q64076369 | Neurological, Psychiatric, and Biochemical Aspects of Thiamine Deficiency in Children and Adults |
| Q34998124 | Neuronal nucleus and cytoplasm volume deficit in children with autism and volume increase in adolescents and adults. |
| Q89477342 | New Horizons for Molecular Genetics Diagnostic and Research in Autism Spectrum Disorder |
| Q59809263 | Oxidative Stress and Nonalcoholic Fatty Liver Disease in Hemodialysis Patients |
| Q37453274 | Oxidative stress induces mitochondrial dysfunction in a subset of autism lymphoblastoid cell lines in a well-matched case control cohort |
| Q92403445 | Peripheral Mitochondrial DNA Copy Number is Increased in Korean Attention-Deficit Hyperactivity Disorder Patients |
| Q34431317 | Potential therapeutic use of the ketogenic diet in autism spectrum disorders |
| Q47370843 | Protein lipoylation: an evolutionarily conserved metabolic regulator of health and disease |
| Q104509573 | Proteomic and mitochondrial adaptations to early-life stress are distinct in juveniles and adults |
| Q27014070 | ROS and brain diseases: the good, the bad, and the ugly |
| Q34254256 | Stereological study of the neuronal number and volume of 38 brain subdivisions of subjects diagnosed with autism reveals significant alterations restricted to the striatum, amygdala and cerebellum |
| Q50061696 | Structural rearrangements in the mitochondrial genome of Drosophila melanogaster induced by elevated levels of the replicative DNA helicase. |
| Q42368371 | The Alterations in Mitochondrial DNA Copy Number and Nuclear-Encoded Mitochondrial Genes in Rat Brain Structures after Cocaine Self-Administration |
| Q38653427 | The Putative Role of Environmental Mercury in the Pathogenesis and Pathophysiology of Autism Spectrum Disorders and Subtypes. |
| Q35246024 | The many roads to mitochondrial dysfunction in neuroimmune and neuropsychiatric disorders |
| Q90264503 | Untargeted Metabolomics for Autism Spectrum Disorders: Current Status and Future Directions |
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