idoxuridine has been researched along with Xeroderma Pigmentosum in 1 studies
Xeroderma Pigmentosum: A rare, pigmentary, and atrophic autosomal recessive disease. It is manifested as an extreme photosensitivity to ULTRAVIOLET RAYS as the result of a deficiency in the enzyme that permits excisional repair of ultraviolet-damaged DNA.
| 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 Xeroderma Pigmentosum
| 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 |