ID   XP10BE
AC   CVCL_U666
SY   Xeroderma Pigmentosum 10 BEthesda; Gor Do; GOR DO
DR   ATCC; CRL-1204
DR   Wikidata; Q54871612
RX   PubMed=273925;
RX   PubMed=1383811;
RX   PubMed=4811796;
CC   Discontinued: ATCC; CRL-1204; true.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C114770; Xeroderma pigmentosum, complementation group C
DI   ORDO; Orphanet_910; Xeroderma pigmentosum
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   16Y
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 10
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RX   PubMed=273925; DOI=10.1073/pnas.75.4.1984; PMCID=PMC392467;
RA   Andrews A.D., Barrett S.F., Robbins J.H.;
RT   "Xeroderma pigmentosum neurological abnormalities correlate with
RT   colony-forming ability after ultraviolet radiation.";
RL   Proc. Natl. Acad. Sci. U.S.A. 75:1984-1988(1978).
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RX   PubMed=1383811; DOI=10.1016/0921-8777(92)90008-Q;
RA   Kantor G.J., Shanower G.A.;
RT   "A re-examination of the intragenome distribution of repaired sites in
RT   proliferating xeroderma pigmentosum complementation group C
RT   fibroblasts.";
RL   Mutat. Res. 293:55-64(1992).
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RX   PubMed=4811796; DOI=10.7326/0003-4819-80-2-221;
RA   Robbins J.H., Kraemer K.H., Lutzner M.A., Festoff B.W., Coon H.G.;
RT   "Xeroderma pigmentosum. An inherited disease with sun sensitivity,
RT   multiple cutaneous neoplasms, and abnormal DNA repair.";
RL   Ann. Intern. Med. 80:221-248(1974).
//