3-aminobenzamide has been researched along with Xeroderma Pigmentosum in 2 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 | 2 (100.00) | 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 | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fujiwara, Y | 1 |
| Goto, K | 1 |
| Yamamoto, K | 1 |
| Ichihashi, M | 1 |
| Karentz, D | 1 |
| Cleaver, JE | 1 |
2 other studies available for 3-aminobenzamide and Xeroderma Pigmentosum
| Article | Year |
|---|---|
Roles of poly(ADP-ribose) synthesis in repair and replication in normal human, Cockayne syndrome, and xeroderma pigmentosum fibroblasts after UV irradiation.
Topics: Benzamides; Cockayne Syndrome; DNA Repair; DNA Replication; Dwarfism; Fibroblasts; Humans; In Vitro | 1983 |
Excision repair in xeroderma pigmentosum group C but not group D is clustered in a small fraction of the total genome.
Topics: Aphidicolin; Benzamides; Cell Line; Chromosome Mapping; Cycloheximide; Cytarabine; Diterpenes; DNA; | 1986 |