w 7 has been researched along with Bloom Syndrome in 1 studies
W 7: RN given refers to parent cpd; structure; calmodulin antagonist
Bloom Syndrome: An autosomal recessive disorder characterized by telangiectatic ERYTHEMA of the face, photosensitivity, DWARFISM and other abnormalities, and a predisposition toward developing cancer. The Bloom syndrome gene (BLM) encodes a RecQ-like DNA helicase.
| 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 |
|---|---|
| Lönn, U | 1 |
| Lönn, S | 1 |
| Nylen, U | 1 |
| Winblad, G | 1 |
1 other study available for w 7 and Bloom Syndrome
| Article | Year |
|---|---|
Increased levels of 5-fluorouracil-induced DNA lesions in Bloom's syndrome.
Topics: Aphidicolin; Bloom Syndrome; Cell Cycle; Cell Line; Diterpenes; DNA; DNA Damage; DNA Glycosylases; D | 1990 |