glutamic acid has been researched along with Mitochondrial Diseases in 21 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 7 (33.33) | 29.6817 |
| 2010's | 13 (61.90) | 24.3611 |
| 2020's | 1 (4.76) | 2.80 |
| Authors | Studies |
|---|---|
| Bitto, A; Bornstein, R; Johnson, SC; Kaeberlein, M; Kayser, EB; Morgan, PG; Pan, A; Park, KY; Raftery, D; Sedensky, MM; Stokes, J; Sun, G | 1 |
| de Bari, L; De Filippis, B; Lacivita, E; Laviola, G; Leopoldo, M; Vacca, RA; Valenti, D; Vigli, D | 1 |
| Chae, U; Kim, MH; Lee, DS; Lee, HJ; Lee, HS; Lee, JY; Lee, SR; Min, JS; Song, KS; Yang, EJ | 1 |
| Chiu, LD; Fujikado, T; Fujita, K; Kanda, H; Kawagoe, H; Morimoto, T; Nakamura, M; Nishida, K; Ozawa, T | 1 |
| De la Rosa, G; Flores, G; Hernández-Echeagaray, E; Mendoza, E; Miranda-Barrientos, JA; Morales-Herrera, E; Ruelas, A; Vázquez-Roque, RA | 1 |
| Cortopassi, GA; Erickson, JD; Horiuchi, M; Jin, LW; Liu, XB; Maezawa, I; Wulff, H | 1 |
| Almeida Silva, LF; Antunes Soares, FA; da Rosa Gerbatin, R; Dobrachinski, F; Ferreira Marques, N; Franco, JL; Freire Royes, LF; Rechia Fighera, M; Sartori, G; Zemolin, AP | 1 |
| Bordoni, A; Bresolin, N; Comi, GP; Corti, S; Crugnola, V; Del Bo, R; Donadoni, C; Fortunato, F; Lucchini, V; Moggio, M; Papadimitriou, D; Ronchi, D; Salani, S; Santoro, D | 1 |
| Bouitbir, J; Chakfe, N; Di Marco, P; Geny, B; Kretz, JG; Piquard, F; Ribera, F; Thaveau, F; Zoll, J | 1 |
| Fülöp, F; Klivényi, P; Toldi, J; Vámos, E; Vécsei, L; Zádori, D | 1 |
| Acin-Perez, R; Enriquez, JA; Kirby, DM; Lightowlers, RN; Nooteboom, M; Smulders-Srinivasan, TK; Trevelyan, AJ; Turnbull, DM; Whittington, MA | 1 |
| Bor-Seng-Shu, E; de Lima Oliveira, M; Teixeira, MJ | 1 |
| Arai, H; Goto, Y; Hatakeyama, H; Kirino, Y; Komaki, H; Mimaki, M; Nishino, I; Nonaka, I; Suzuki, T; Yokoyama, M | 1 |
| Calcagno, E; Cantoni, L; D'Alessandro, G; Invernizzi, RW; Rizzardini, M; Tartari, S | 1 |
| Audhya, T; Geier, DA; Geier, MR; Kern, JK; King, PG; Sykes, LK | 1 |
| Fujiwara, T; Morimoto, K | 1 |
| Anglin, RE; Mazurek, MF; Noseworthy, MD; Rosebush, PI; Tarnopolsky, M | 1 |
| Förster, H; Huemer, M; Idriceanu, C; Kamper, A; Mayr, JA; Moslemi, AR; Muss, W; Oldfors, A; Sperl, W | 1 |
| Chan, SS; Copeland, WC; Longley, MJ | 1 |
| Almeida, J; Ataíde, A; Borges, L; Correia, C; Coutinho, AM; Diogo, L; Grazina, M; Marques, C; Miguel, T; Oliveira, C; Oliveira, G; Vicente, AM | 1 |
| Del Río, P; Massieu, L | 1 |
2 review(s) available for glutamic acid and Mitochondrial Diseases
| Article | Year |
|---|---|
Kynurenines in chronic neurodegenerative disorders: future therapeutic strategies.
Topics: Animals; Brain; Glutamic Acid; Humans; Kynurenic Acid; Mitochondrial Diseases; NAD; Neurodegenerative Diseases; Neuroprotective Agents; Phosphatidylinositol 3-Kinases; Phosphoinositide-3 Kinase Inhibitors; Quinolinic Acid; Tryptophan | 2009 |
Evidence of parallels between mercury intoxication and the brain pathology in autism.
Topics: Amyloid beta-Protein Precursor; Animals; Autistic Disorder; Brain; Calcium; Cerebellum; Cytokines; Encephalitis; Endothelium, Vascular; gamma-Aminobutyric Acid; Glutamic Acid; Homeostasis; Humans; Insulin-Like Growth Factor I; Lipid Peroxidation; Mercury Poisoning, Nervous System; Microglia; Microtubules; Mitochondrial Diseases; Neurites; NF-kappa B; Oxidative Stress | 2012 |
19 other study(ies) available for glutamic acid and Mitochondrial Diseases
| Article | Year |
|---|---|
Regional metabolic signatures in the Ndufs4(KO) mouse brain implicate defective glutamate/α-ketoglutarate metabolism in mitochondrial disease.
Topics: Animals; Brain; Disease Models, Animal; Electron Transport Complex I; Female; Glutamic Acid; Ketoglutaric Acids; Leigh Disease; Male; Metabolome; Mice; Mice, Inbred C57BL; Mice, Knockout; Mitochondrial Diseases; TOR Serine-Threonine Kinases | 2020 |
Stimulation of the brain serotonin receptor 7 rescues mitochondrial dysfunction in female mice from two models of Rett syndrome.
Topics: Adenosine Triphosphate; Animals; Brain; Disease Models, Animal; Female; Glucosephosphate Dehydrogenase; Glutamic Acid; Histocompatibility Antigens; Horseradish Peroxidase; Methyl-CpG-Binding Protein 2; Mice; Mice, Inbred C57BL; Mice, Transgenic; Mitochondrial Diseases; NADP; Piperazines; Reactive Oxygen Species; Receptors, Serotonin; Rett Syndrome; Serotonin Receptor Agonists; Superoxide Dismutase | 2017 |
Oleuropein isolated from Fraxinus rhynchophylla inhibits glutamate-induced neuronal cell death by attenuating mitochondrial dysfunction.
Topics: Animals; Apoptosis; bcl-2-Associated X Protein; Cell Death; Cell Line; Dynamins; Fraxinus; Gene Expression Regulation; Glutamic Acid; Hippocampus; Iridoid Glucosides; Iridoids; Mice; Mitochondria; Mitochondrial Diseases; Neurodegenerative Diseases; Neurons; Neuroprotective Agents; Oxidative Stress; Phosphorylation; Proto-Oncogene Proteins c-bcl-2 | 2018 |
Using redox-sensitive mitochondrial cytochrome Raman bands for label-free detection of mitochondrial dysfunction.
Topics: Animals; Cell Line; Cytochromes; Glutamic Acid; Mice; Mitochondria; Mitochondrial Diseases; Oxidation-Reduction; Spectrum Analysis, Raman | 2019 |
In vivo mitochondrial inhibition alters corticostriatal synaptic function and the modulatory effects of neurotrophins.
Topics: Animals; Brain-Derived Neurotrophic Factor; Cerebral Cortex; Corpus Striatum; Glutamic Acid; Male; Mice, Inbred C57BL; Mitochondria; Mitochondrial Diseases; Nerve Growth Factors; Neural Pathways; Neurotrophin 3; Nitro Compounds; Propionates; Random Allocation; Receptors, Nerve Growth Factor; Synapses; Synaptic Transmission; Tissue Culture Techniques | 2014 |
Dysregulation of glutamine transporter SNAT1 in Rett syndrome microglia: a mechanism for mitochondrial dysfunction and neurotoxicity.
Topics: Adenosine Triphosphate; Amino Acid Transport System A; Animals; Glutamic Acid; Glycine; Methyl-CpG-Binding Protein 2; Mice; Mice, Inbred C57BL; Mice, Knockout; Microglia; Mitochondrial Diseases; Neurotoxicity Syndromes; Oxygen Consumption; Primary Cell Culture; Rett Syndrome | 2015 |
Regulation of Mitochondrial Function and Glutamatergic System Are the Target of Guanosine Effect in Traumatic Brain Injury.
Topics: Amino Acid Transport System X-AG; Animals; Brain Injuries, Traumatic; Disease Models, Animal; Glutamic Acid; Guanosine; Male; Mitochondrial Diseases; Oxidation-Reduction; Rats; Rats, Wistar | 2017 |
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction.
Topics: Adult; Amyotrophic Lateral Sclerosis; Arginine; Cytochromes c; DNA Mutational Analysis; Family Health; Genetic Linkage; Genetic Predisposition to Disease; Glutamic Acid; Humans; Male; Mitochondria, Muscle; Mitochondrial Diseases; Mutation; Superoxide Dismutase; Superoxide Dismutase-1 | 2009 |
Contralateral leg as a control during skeletal muscle ischemia-reperfusion.
Topics: Animals; Ascorbic Acid; Cell Respiration; Electron Transport Chain Complex Proteins; Glutamic Acid; Ischemia; Lower Extremity; Malates; Male; Mitochondria, Muscle; Mitochondrial Diseases; Muscle, Skeletal; Rats; Rats, Wistar; Reperfusion Injury; Succinic Acid; Tetramethylphenylenediamine | 2009 |
Mitochondrial DNA mutations affect calcium handling in differentiated neurons.
Topics: Aniline Compounds; Animals; Calcium; Calcium Channels; Cell Line; DNA, Mitochondrial; Embryonic Stem Cells; Female; Fluoresceins; Glutamic Acid; Intracellular Space; Kinetics; Membrane Potentials; Mice; Mitochondrial Diseases; Mutation; Neurons; Patch-Clamp Techniques; Receptors, N-Methyl-D-Aspartate; Time Factors | 2010 |
Traumatic brain injury and metabolism.
Topics: Blood Flow Velocity; Blood Glucose; Brain; Brain Injuries; Craniotomy; Decompression, Surgical; Energy Metabolism; Glutamic Acid; Humans; Intracranial Pressure; Lactic Acid; Mitochondrial Diseases; Oxygen Consumption; Prognosis; Pyruvic Acid; Treatment Outcome | 2010 |
Reversible infantile respiratory chain deficiency: a clinical and molecular study.
Topics: Adolescent; Brain; Child; Child, Preschool; DNA Mutational Analysis; DNA, Mitochondrial; Electron Transport Complex IV; Female; Glutamic Acid; Humans; Infant; Magnetic Resonance Imaging; Male; Mitochondria, Muscle; Mitochondrial Diseases; Muscle, Skeletal; Mutation; RNA, Transfer | 2010 |
Glutamate and glutathione interplay in a motor neuronal model of amyotrophic lateral sclerosis reveals altered energy metabolism.
Topics: Amyotrophic Lateral Sclerosis; Animals; Cell Communication; Cell Line; Disease Models, Animal; Energy Metabolism; Glutamic Acid; Glutathione; Humans; Mice; Mice, Transgenic; Mitochondrial Diseases; Models, Neurological; Motor Neurons | 2011 |
Inhibition of p53 transactivation functionally interacts with microtubule stabilization to suppress excitotoxicity-induced axon degeneration.
Topics: Animals; Axons; Benzothiazoles; Cells, Cultured; Dynactin Complex; Glutamic Acid; Hippocampus; Microtubule-Associated Proteins; Microtubules; Mitochondria; Mitochondrial Diseases; Nerve Degeneration; Neurotoxins; Paclitaxel; Rats; Rats, Wistar; Toluene; Transcriptional Activation; Tumor Suppressor Protein p53 | 2012 |
Psychiatric symptoms correlate with metabolic indices in the hippocampus and cingulate in patients with mitochondrial disorders.
Topics: Adult; Aged; Anxiety; Aspartic Acid; Case-Control Studies; Caudate Nucleus; Creatine; Female; Glutamic Acid; Glutamine; Glycerylphosphorylcholine; Gyrus Cinguli; Hippocampus; Humans; Inositol; Magnetic Resonance Spectroscopy; Male; Middle Aged; Mitochondrial Diseases; Psychiatric Status Rating Scales | 2012 |
A novel sporadic mutation G14739A of the mitochondrial tRNA(Glu) in a girl with exercise intolerance.
Topics: Brain; Child; DNA Mutational Analysis; Exercise Tolerance; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Mitochondrial Diseases; Mitochondrial Myopathies; Muscle Fibers, Skeletal; Muscle Weakness; Muscle, Skeletal; Mutation; RNA; RNA, Mitochondrial; RNA, Transfer | 2006 |
Modulation of the W748S mutation in DNA polymerase gamma by the E1143G polymorphismin mitochondrial disorders.
Topics: Amino Acid Sequence; Amino Acid Substitution; Catalytic Domain; DNA; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Enzyme Stability; Glutamic Acid; Glycine; Humans; Mitochondrial Diseases; Models, Molecular; Molecular Sequence Data; Mutation; Nucleotides; Polymorphism, Genetic; Protein Conformation; Serine; Tryptophan | 2006 |
Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: no association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene.
Topics: Aspartic Acid; Autistic Disorder; Chromosome Mapping; DNA Mutational Analysis; DNA Primers; DNA, Mitochondrial; Gene Expression; Gene Frequency; Glutamic Acid; Haplotypes; Humans; Lactic Acid; Membrane Transport Proteins; Mitochondrial Diseases; Mitochondrial Membrane Transport Proteins; Mitochondrial Proteins; Pyruvic Acid | 2006 |
Mild mitochondrial inhibition in vivo enhances glutamate-induced neuronal damage through calpain but not caspase activation: role of ionotropic glutamate receptors.
Topics: Animals; Brain Diseases, Metabolic; Calpain; Caspase 3; Cell Death; Enzyme Activation; Excitatory Amino Acid Antagonists; Glutamic Acid; Male; Mitochondria; Mitochondrial Diseases; Nerve Degeneration; Neurotoxins; Rats; Rats, Wistar; Receptors, Glutamate; Receptors, N-Methyl-D-Aspartate; Signal Transduction | 2008 |