ID   CSH696CTO
AC   CVCL_ZS11
SY   Cockayne Syndrome Heterozygote 696 Canada TOronto
DR   Wikidata; Q98125787
RX   PubMed=157803;
RX   PubMed=7360141;
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   44Y
CA   Finite cell line
DT   Created: 02-07-20; Last updated: 29-06-23; Version: 6
//
RX   PubMed=157803;
RA   Lehmann A.R., Kirk-Bell S., Mayne L.V.;
RT   "Abnormal kinetics of DNA synthesis in ultraviolet light-irradiated
RT   cells from patients with Cockayne's syndrome.";
RL   Cancer Res. 39:4237-4241(1979).
//
RX   PubMed=7360141; DOI=10.1016/0027-5107(80)90180-3;
RA   Marshall R.R., Arlett C.F., Harcourt S.A., Broughton B.C.;
RT   "Increased sensitivity of cell strains from Cockayne's syndrome to
RT   sister-chromatid-exchange induction and cell killing by UV light.";
RL   Mutat. Res. 69:107-112(1980).
//