glutamic acid has been researched along with Dementias, Transmissible in 8 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (12.50) | 18.2507 |
2000's | 3 (37.50) | 29.6817 |
2010's | 4 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bertoli, A; Sorgato, MC | 1 |
Aguzzi, A; Bremer, J; Craveiro, M; Cudalbu, C; Gruetter, R; Mlynárik, V | 1 |
Brajusković, G; Cadez, I; Dimitrijević, R; Dobricić, V; Keckarević, D; Keckarević-Marković, M; Kecmanović, M; Romac, S; Savić-Pavićević, D | 1 |
Bertani, I; Canovi, M; Chiesa, R; Colleoni, S; Condliffe, SB; Dolphin, AC; Forloni, G; Gobbi, M; Mantovani, S; Matteoli, M; Micotti, E; Morini, R; Restelli, E; Senatore, A; Verderio, C | 1 |
Bate, C; Gravenor, M; Reid, S; Rutherford, S; Williams, A | 1 |
Brown, DR; Daniels, M; Sassoon, J | 1 |
Anthony, DC; Blamire, AM; Broom, KA; Griffin, JL; Lowe, JP; Perry, VH; Scott, H; Sibson, NR; Styles, P | 1 |
Scallet, AC; Ye, X | 1 |
1 review(s) available for glutamic acid and Dementias, Transmissible
Article | Year |
---|---|
Excitotoxic mechanisms of neurodegeneration in transmissible spongiform encephalopathies.
Topics: Animals; Brain; Cricetinae; Glutamic Acid; Humans; Hypothalamus; Ibogaine; Kainic Acid; Mice; N-Methylaspartate; Nerve Degeneration; Neurotoxins; Prion Diseases | 1997 |
7 other study(ies) available for glutamic acid and Dementias, Transmissible
Article | Year |
---|---|
Neuronal pathophysiology featuring PrP
Topics: Alzheimer Disease; Animals; Calcium; Cell Membrane; Cytosol; Glutamic Acid; Humans; Mice; Mice, Knockout; Mitochondria; Neurons; Neurotoxins; Primary Cell Culture; Prion Diseases; PrPC Proteins | 2018 |
In Vivo Longitudinal (1)H MRS Study of Transgenic Mouse Models of Prion Disease in the Hippocampus and Cerebellum at 14.1 T.
Topics: Animals; Aspartic Acid; Brain Chemistry; Cerebellum; Glutamic Acid; Hippocampus; Inositol; Lactic Acid; Magnetic Resonance Spectroscopy; Mice; Mice, Inbred BALB C; Mice, Knockout; Mice, Transgenic; Prion Diseases; Prion Proteins; Prions | 2015 |
Polymorphisms of the prion protein gene (PRNP) in a Serbian population.
Topics: Amino Acid Substitution; Female; Genetic Predisposition to Disease; Genetic Testing; Glutamic Acid; Humans; Lysine; Male; Mutagenesis, Insertional; Oligopeptides; Polymorphism, Genetic; Prion Diseases; Prion Proteins; Prions; Repetitive Sequences, Amino Acid; Sequence Deletion; Serbia | 2010 |
Mutant PrP suppresses glutamatergic neurotransmission in cerebellar granule neurons by impairing membrane delivery of VGCC α(2)δ-1 Subunit.
Topics: Age Factors; Animals; Animals, Newborn; Biophysics; Calcium; Calcium Channels; Cells, Cultured; Cerebellum; Disease Models, Animal; Electric Stimulation; Endoplasmic Reticulum; Glutamic Acid; Green Fluorescent Proteins; Magnetic Resonance Imaging; Membrane Potentials; Mice; Mice, Inbred C57BL; Mice, Transgenic; Motor Activity; Mutation; Neurons; Patch-Clamp Techniques; Prion Diseases; Prion Proteins; Prions; Protein Transport; Reaction Time; Rotarod Performance Test; Synaptic Transmission; Synaptosomes | 2012 |
Cyclo-oxygenase inhibitors protect against prion-induced neurotoxicity in vitro.
Topics: Animals; Animals, Newborn; Anti-Inflammatory Agents, Non-Steroidal; Cell Survival; Cerebral Cortex; Cyclooxygenase 1; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Cyclooxygenase Inhibitors; Dinoprostone; Dose-Response Relationship, Drug; Enzyme Inhibitors; Fetus; Glutamic Acid; Isoenzymes; Membrane Proteins; Mice; Mice, Inbred C57BL; Microglia; Neuroblastoma; Neurons; Neuroprotective Agents; Peptide Fragments; Prion Diseases; Prions; Prostaglandin-Endoperoxide Synthases; PrPSc Proteins; Tumor Cells, Cultured | 2002 |
Astrocytic regulation of NMDA receptor subunit composition modulates the toxicity of prion peptide PrP106-126.
Topics: Animals; Animals, Newborn; Arachidonic Acid; Astrocytes; Cell Communication; Cells, Cultured; Coculture Techniques; Copper; Excitatory Amino Acid Antagonists; Glutamic Acid; Nerve Degeneration; Neurons; Peptide Fragments; Prion Diseases; Prions; Protein Subunits; Rats; Rats, Sprague-Dawley; Receptors, N-Methyl-D-Aspartate | 2004 |
MRI and MRS alterations in the preclinical phase of murine prion disease: association with neuropathological and behavioural changes.
Topics: Animals; Aspartic Acid; Astrocytes; Body Water; Brain; Choline; Creatine; Diffusion; Disease Models, Animal; Disease Progression; Gliosis; Glucose; Glutamic Acid; Hyperkinesis; Inositol; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Mice; Mice, Inbred C57BL; Microglia; Prion Diseases | 2007 |