thymine has been researched along with Hepatolenticular Degeneration in 1 studies
Hepatolenticular Degeneration: A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding copper-transporting ATPase 2 (EC 3.6.3.4), also known as the Wilson disease protein. The overload of copper inevitably leads to progressive liver and neurological dysfunction such as LIVER CIRRHOSIS; TREMOR; ATAXIA and intellectual deterioration. Hepatic dysfunction may precede neurologic dysfunction by several years.
| 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 | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Wang, J | 1 |
| Cao, H | 1 |
| You, C | 1 |
| Yuan, B | 1 |
| Bahde, R | 1 |
| Gupta, S | 1 |
| Nishigori, C | 1 |
| Niedernhofer, LJ | 1 |
| Brooks, PJ | 1 |
| Wang, Y | 1 |
1 other study available for thymine and Hepatolenticular Degeneration
| Article | Year |
|---|---|
Endogenous formation and repair of oxidatively induced G[8-5 m]T intrastrand cross-link lesion.
Topics: Animals; DNA; DNA Damage; DNA Repair; Guanine; Hepatolenticular Degeneration; Humans; Liver; Mice; O | 2012 |