thymidine has been researched along with Cockayne Syndrome in 2 studies
Cockayne Syndrome: A syndrome characterized by multiple system abnormalities including DWARFISM; PHOTOSENSITIVITY DISORDERS; PREMATURE AGING; and HEARING LOSS. It is caused by mutations of a number of autosomal recessive genes encoding proteins that involve transcriptional-coupled DNA REPAIR processes. Cockayne syndrome is classified by the severity and age of onset. Type I (classical; CSA) is early childhood onset in the second year of life; type II (congenital; CSB) is early onset at birth with severe symptoms; type III (xeroderma pigmentosum; XP) is late childhood onset with mild symptoms.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (50.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Nergadze, SG | 1 |
Pleskach, NM | 1 |
Mikhel'son, VM | 1 |
Prokof'eva, VV | 1 |
Barenfel'd, LS | 1 |
Suzuki, N | 1 |
Watanabe, I | 1 |
Nishimaki, J | 1 |
Fuse, A | 1 |
Sugita, K | 1 |
Sekiya, S | 1 |
Takakubo, Y | 1 |
Terao, K | 1 |
2 other studies available for thymidine and Cockayne Syndrome
Article | Year |
---|---|
[DNA replication in intact and X-ray-irradiated cells in the Cockayne syndrome].
Topics: Autoradiography; Cells, Cultured; Cockayne Syndrome; DNA Replication; Fibroblasts; Humans; Male; Thy | 1993 |
Increased resistance to the anticellular effect of interferon in an ultraviolet light-resistant human cell line, UVr-1.
Topics: 2',5'-Oligoadenylate Synthetase; Cell Division; Cell Line; Cockayne Syndrome; Deoxyadenosines; DNA R | 1986 |