Cellosaurus logo
expasy logo

Cellosaurus XP10BE (CVCL_U666)

[Text version]
Cell line name XP10BE
Synonyms Xeroderma Pigmentosum 10 BEthesda; Gor Do; GOR DO
Accession CVCL_U666
Resource Identification Initiative To cite this cell line use: XP10BE (RRID:CVCL_U666)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Xeroderma pigmentosum, complementation group C (NCIt: C114770)
Xeroderma pigmentosum (ORDO: Orphanet_910)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 16Y
Category Finite cell line
Publications

PubMed=4811796; DOI=10.7326/0003-4819-80-2-221
Robbins J.H., Kraemer K.H., Lutzner M.A., Festoff B.W., Coon H.G.
Xeroderma pigmentosum. An inherited disease with sun sensitivity, multiple cutaneous neoplasms, and abnormal DNA repair.
Ann. Intern. Med. 80:221-248(1974)

PubMed=273925; DOI=10.1073/pnas.75.4.1984; PMCID=PMC392467
Andrews A.D., Barrett S.F., Robbins J.H.
Xeroderma pigmentosum neurological abnormalities correlate with colony-forming ability after ultraviolet radiation.
Proc. Natl. Acad. Sci. U.S.A. 75:1984-1988(1978)

PubMed=1383811; DOI=10.1016/0921-8777(92)90008-Q
Kantor G.J., Shanower G.A.
A re-examination of the intragenome distribution of repaired sites in proliferating xeroderma pigmentosum complementation group C fibroblasts.
Mutat. Res. 293:55-64(1992)

Cross-references
Cell line collections (Providers) ATCC; CRL-1204 - Discontinued
Encyclopedic resources Wikidata; Q54871612
Entry history
Entry creation16-Apr-2014
Last entry update29-Jun-2023
Version number10