hydroxyurea has been researched along with Cockayne Syndrome in 3 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 | 2 (66.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Squires, S | 1 |
| Johnson, RT | 1 |
| Cleaver, JE | 1 |
| Wong, JM | 1 |
| Ingles, CJ | 1 |
3 other studies available for hydroxyurea and Cockayne Syndrome
| Article | Year |
|---|---|
U.v. induces long-lived DNA breaks in Cockayne's syndrome and cells from an immunodeficient individual (46BR): defects and disturbance in post incision steps of excision repair.
Topics: Cells, Cultured; Cockayne Syndrome; Culture Media; Cytarabine; DNA Repair; Dose-Response Relationshi | 1983 |
Sensitivity of excision repair in normal human, xeroderma pigmentosum variant and Cockayne's syndrome fibroblasts to inhibition by cytosine arabinoside.
Topics: Cockayne Syndrome; Cytarabine; DNA Repair; DNA, Single-Stranded; Dwarfism; Fibroblasts; Humans; Hydr | 1981 |
A compromised yeast RNA polymerase II enhances UV sensitivity in the absence of global genome nucleotide excision repair.
Topics: Adenosine Triphosphatases; Cockayne Syndrome; DNA Repair; DNA-Binding Proteins; Fungal Proteins; Gen | 2001 |