Page last updated: 2024-11-06

thymidine and Cockayne Syndrome

thymidine 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.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's1 (50.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Nergadze, SG1
Pleskach, NM1
Mikhel'son, VM1
Prokof'eva, VV1
Barenfel'd, LS1
Suzuki, N1
Watanabe, I1
Nishimaki, J1
Fuse, A1
Sugita, K1
Sekiya, S1
Takakubo, Y1
Terao, K1

Other Studies

2 other studies available for thymidine and Cockayne Syndrome

ArticleYear
[DNA replication in intact and X-ray-irradiated cells in the Cockayne syndrome].
    Tsitologiia, 1993, Volume: 35, Issue:9

    Topics: Autoradiography; Cells, Cultured; Cockayne Syndrome; DNA Replication; Fibroblasts; Humans; Male; Thy

1993
Increased resistance to the anticellular effect of interferon in an ultraviolet light-resistant human cell line, UVr-1.
    The Journal of general virology, 1986, Volume: 67 ( Pt 4)

    Topics: 2',5'-Oligoadenylate Synthetase; Cell Division; Cell Line; Cockayne Syndrome; Deoxyadenosines; DNA R

1986