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Cellosaurus XP8LO (CVCL_ZN87)

[Text version]
Cell line name XP8LO
Synonyms Xeroderma Pigmentosum 8 LOndon
Accession CVCL_ZN87
Resource Identification Initiative To cite this cell line use: XP8LO (RRID:CVCL_ZN87)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Xeroderma pigmentosum, complementation group A (NCIt: C3965)
Xeroderma pigmentosum (ORDO: Orphanet_910)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 2-3Y
Category Finite cell line
Publications

PubMed=1034206; DOI=10.1016/0027-5107(76)90044-0
de Weerd-Kastelein E.A., Keijzer W., Sabour M., Parrington J.M., Bootsma D.
A xeroderma pigmentosum patient having a high residual activity of unscheduled DNA synthesis after UV is assigned to complementation group A.
Mutat. Res. 37:307-312(1976)

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=3724780; DOI=10.1016/0167-8817(86)90043-x
Kantor G.J., Player A.N.
A further definition of characteristics of DNA-excision repair in xeroderma pigmentosum complementation group A strains.
Mutat. Res. 166:79-88(1986)

DOI=10.1007/978-1-4757-5016-4_9
Jaspers N.G.J., Roza L., Vermeulen W., Eker A.P.M., Taalman R.D.F.M., Hoeijmakers J.H.J., Bootsma D.
In vitro correction of cells from patients with mutagen hypersensitivity.
(In book chapter) DNA damage and repair; Castellani A. (eds.); pp.73-82; Springer; Boston; USA (1989)

PubMed=1702221; DOI=10.1073/pnas.87.24.9908; PMCID=PMC55283
Satokata I., Tanaka K., Miura N., Miyamoto I., Satoh Y., Kondo S., Okada Y.
Characterization of a splicing mutation in group A xeroderma pigmentosum.
Proc. Natl. Acad. Sci. U.S.A. 87:9908-9912(1990)

PubMed=2065254; DOI=10.1093/brain/114.3.1335
Robbins J.H., Brumback R.A., Mendiones M., Barrett S.F., Carl J.R., Cho S., Denckla M.B., Ganges M.B., Gerber L.H., Guthrie R.A., Meer J., Moshell A.N., Polinsky R.J., Ravin P.D., Sonies B.C., Tarone R.E.
Neurological disease in xeroderma pigmentosum. Documentation of a late onset type of the juvenile onset form.
Brain 114:1335-1361(1991)

PubMed=1372102; DOI=10.1016/0921-8777(92)90080-M
Satokata I., Tanaka K., Miura N., Narita M., Mimaki T., Satoh Y., Kondo S., Okada Y.
Three nonsense mutations responsible for group A xeroderma pigmentosum.
Mutat. Res. 273:193-202(1992)

Cross-references
Cell line collections (Providers) ATCC; CRL-1376 - Discontinued
Encyclopedic resources Wikidata; Q98136185
Entry history
Entry creation02-Jul-2020
Last entry update29-Jun-2023
Version number6