dithiothreitol has been researched along with Motor Neuron Disease in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hayward, LJ; Tiwari, A | 1 |
| Carrì, MT; Casciati, A; Ferri, A; Gabbianelli, R; Paolucci, E; Rotilio, G | 1 |
2 other study(ies) available for dithiothreitol and Motor Neuron Disease
| Article | Year |
|---|---|
Familial amyotrophic lateral sclerosis mutants of copper/zinc superoxide dismutase are susceptible to disulfide reduction.
Topics: Amino Acid Substitution; Animals; Binding Sites; Cysteine; Disulfides; Dithiothreitol; Humans; Iodoacetamide; Kinetics; Mice; Motor Neuron Disease; Mutagenesis, Site-Directed; Mutation; Organ Specificity; Oxidation-Reduction; Protein Structure, Secondary; Recombinant Proteins; Superoxide Dismutase | 2003 |
Calcineurin activity is regulated both by redox compounds and by mutant familial amyotrophic lateral sclerosis-superoxide dismutase.
Topics: Animals; Ascorbic Acid; Calcineurin; Calcium; Dithiothreitol; Hippocampus; Humans; Mice; Mice, Transgenic; Motor Cortex; Motor Neuron Disease; Neuroblastoma; Oxidation-Reduction; Oxidative Stress; Recombinant Proteins; Spinal Cord; Superoxide Dismutase; Transfection; Tumor Cells, Cultured | 2000 |