cytosine has been researched along with Cockayne Syndrome in 2 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 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chaim, IA | 1 |
| Gardner, A | 1 |
| Wu, J | 1 |
| Iyama, T | 1 |
| Wilson, DM | 1 |
| Samson, LD | 1 |
| Selzer, RR | 1 |
| Nyaga, S | 1 |
| Tuo, J | 1 |
| May, A | 1 |
| Muftuoglu, M | 1 |
| Christiansen, M | 1 |
| Citterio, E | 1 |
| Brosh, RM | 1 |
| Bohr, VA | 1 |
2 other studies available for cytosine and Cockayne Syndrome
| Article | Year |
|---|---|
A novel role for transcription-coupled nucleotide excision repair for the in vivo repair of 3,N4-ethenocytosine.
Topics: Adenine; Animals; Cell Line; Cells, Cultured; Cockayne Syndrome; Cytosine; DNA Adducts; DNA Repair; | 2017 |
Differential requirement for the ATPase domain of the Cockayne syndrome group B gene in the processing of UV-induced DNA damage and 8-oxoguanine lesions in human cells.
Topics: Adenosine Triphosphatases; Amino Acid Motifs; Amino Acid Sequence; Apoptosis; Cell Extracts; Cell Li | 2002 |