trifluoperazine 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 | 1 (100.00) | 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 |
|---|---|
| Aggeler, J | 1 |
| Murnane, JP | 1 |
1 other study available for trifluoperazine and Xeroderma Pigmentosum
| Article | Year |
|---|---|
Enhanced expression of procollagenase in ataxia-telangiectasia and xeroderma pigmentosum fibroblasts.
Topics: Ataxia Telangiectasia; Collagenases; Enzyme Precursors; Fibroblasts; Gene Expression Regulation, Enz | 1990 |