cytosine has been researched along with TDP-43 Proteinopathies in 1 studies
TDP-43 Proteinopathies: Diseases characterized by the presence of abnormally phosphorylated, ubiquitinated, and cleaved DNA-binding protein TDP-43 in affected brain and spinal cord. Inclusions of the pathologic protein in neurons and glia, without the presence of AMYLOID, is the major feature of these conditions, thus making these proteinopathies distinct from most other neurogenerative disorders in which protein misfolding leads to brain amyloidosis. Both frontotemporal lobar degeneration and AMYOTROPHIC LATERAL SCLEROSIS exhibit this common method of pathogenesis and thus they may represent two extremes of a continuous clinicopathological spectrum of one disease.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Appleby-Mallinder, C | 1 |
| Schaber, E | 1 |
| Kirby, J | 1 |
| Shaw, PJ | 1 |
| Cooper-Knock, J | 1 |
| Heath, PR | 1 |
| Highley, JR | 1 |
1 other study available for cytosine and TDP-43 Proteinopathies
| Article | Year |
|---|---|
TDP43 proteinopathy is associated with aberrant DNA methylation in human amyotrophic lateral sclerosis.
Topics: Amyotrophic Lateral Sclerosis; Cytosine; DNA Methylation; DNA-Binding Proteins; Epigenesis, Genetic; | 2021 |