glutamic acid has been researched along with Hereditary Optic Neuroretinopathy in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 5 (83.33) | 29.6817 |
| 2010's | 1 (16.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, SJ; Chen, WS; Chien, CS; Chiou, GY; Chiou, SH; Hsu, CC; Hwang, DK; Lin, TC; Lin, TW; Nguyen, PNN; Peng, CH; Tsai, CY; Yang, YP; Yarmishyn, AA | 1 |
| Beretta, S; Carelli, V; Fantin, M; Ferrarese, C; Martinuzzi, A; Montopoli, M; Presutto, P; Sala, G; Tremolizzo, L; Trombin, F | 1 |
| Achilli, A; Barbiroli, B; Barboni, P; Baruzzi, A; Bucchi, L; Carelli, V; Dotti, M; Federico, A; Ghelli, A; Lodi, R; Lugaresi, A; Rengo, C; Torroni, A; Valentino, ML | 1 |
| Beretta, S; Carelli, V; Ferrarese, C; Osborne, NN; Wood, JP | 1 |
| Beretta, S; Derham, B; Ferrarese, C; Osborne, NN; Sala, G; Tremolizzo, L; Wood, JP | 1 |
| Hoegger, MJ; Levin, LA; Lieven, CJ | 1 |
6 other study(ies) available for glutamic acid and Hereditary Optic Neuroretinopathy
| Article | Year |
|---|---|
Glutamate Stimulation Dysregulates AMPA Receptors-Induced Signal Transduction Pathway in Leber's Inherited Optic Neuropathy Patient-Specific hiPSC-Derived Retinal Ganglion Cells.
Topics: alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid; Base Sequence; Cell Differentiation; Down-Regulation; Glutamic Acid; Humans; Induced Pluripotent Stem Cells; Optic Atrophy, Hereditary, Leber; Protein Binding; Receptors, AMPA; Retinal Ganglion Cells; Signal Transduction | 2019 |
Antioxidants partially restore glutamate transport defect in leber hereditary optic neuropathy cybrids.
Topics: Antioxidants; Biological Transport; Cell Line; Glutamic Acid; Humans; Hybrid Cells; Optic Atrophy, Hereditary, Leber; Protein Carbonylation | 2008 |
The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy.
Topics: Adult; Aged; DNA Mutational Analysis; DNA, Mitochondrial; Family Health; Female; Ferricyanides; Glutamic Acid; Haplotypes; Humans; Inhibitory Concentration 50; Lysine; Magnetic Resonance Spectroscopy; Male; Microscopy, Electron, Transmission; Middle Aged; Mitochondria, Muscle; Models, Molecular; Muscle, Skeletal; Mutation; NAD; NADH Dehydrogenase; Occipital Lobe; Optic Atrophy, Hereditary, Leber; Pedigree; Polymorphism, Restriction Fragment Length; Radionuclide Imaging; Rotenone; Sequence Analysis, Protein; Succinate Dehydrogenase; Visual Acuity; Visual Fields | 2004 |
Pathogenesis of retinal ganglion cell death in Leber hereditary optic neuropathy (LHON): possible involvement of mitochondria, light and glutamate.
Topics: Cell Death; DNA, Mitochondrial; Glutamic Acid; Humans; Light; Mitochondria; Optic Atrophy, Hereditary, Leber; Retinal Ganglion Cells | 2006 |
Partial mitochondrial complex I inhibition induces oxidative damage and perturbs glutamate transport in primary retinal cultures. Relevance to Leber Hereditary Optic Neuropathy (LHON).
Topics: Animals; Animals, Newborn; Cell Death; Cells, Cultured; Dose-Response Relationship, Drug; Electron Transport Complex I; Energy Metabolism; Excitatory Amino Acid Transporter 1; Free Radicals; Glutamic Acid; Lipid Peroxidation; Mitochondria; Neuroglia; Neurons; Optic Atrophy, Hereditary, Leber; Oxidative Stress; Rats; Rats, Wistar; Retina; Retinal Ganglion Cells; Rotenone; Uncoupling Agents | 2006 |
Differential production of superoxide by neuronal mitochondria.
Topics: Animals; Cell Line; Electron Transport Complex I; Electron Transport Complex III; Energy Metabolism; Glutamic Acid; Heredodegenerative Disorders, Nervous System; Mitochondria; Neurons; Optic Atrophy, Hereditary, Leber; Oxidative Stress; Rats; Rats, Long-Evans; Retinal Ganglion Cells; Succinic Acid; Superoxides; Uncoupling Agents | 2008 |