idoxuridine has been researched along with Cockayne Syndrome in 1 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 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Svetlova, M | 1 |
| Solovjeva, L | 1 |
| Pleskach, N | 1 |
| Yartseva, N | 1 |
| Yakovleva, T | 1 |
| Tomilin, N | 1 |
| Hanawalt, P | 1 |
1 other study available for idoxuridine and Cockayne Syndrome
| Article | Year |
|---|---|
Clustered sites of DNA repair synthesis during early nucleotide excision repair in ultraviolet light-irradiated quiescent human fibroblasts.
Topics: Amanitins; Cell Nucleus; Cells, Cultured; Chromatin; Chromosomes; Cockayne Syndrome; DNA; DNA Damage | 2002 |