ID   XP8LO
AC   CVCL_ZN87
SY   Xeroderma Pigmentosum 8 LOndon
DR   ATCC; CRL-1376
DR   Wikidata; Q98136185
RX   DOI=10.1007/978-1-4757-5016-4_9;
RX   PubMed=273925;
RX   PubMed=1034206;
RX   PubMed=1372102;
RX   PubMed=1702221;
RX   PubMed=2065254;
RX   PubMed=3724780;
CC   Discontinued: ATCC; CRL-1376; true.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C3965; Xeroderma pigmentosum, complementation group A
DI   ORDO; Orphanet_910; Xeroderma pigmentosum
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   2-3Y
CA   Finite cell line
DT   Created: 02-07-20; Last updated: 29-06-23; Version: 6
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RX   DOI=10.1007/978-1-4757-5016-4_9;
RA   Jaspers N.G.J., Roza L., Vermeulen W., Eker A.P.M., Taalman R.D.F.M.,
RA   Hoeijmakers J.H.J., Bootsma D.;
RT   "In vitro correction of cells from patients with mutagen
RT   hypersensitivity.";
RL   (In book chapter) DNA damage and repair; Castellani A. (eds.); pp.73-82; Springer; Boston; USA (1989).
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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=1034206; DOI=10.1016/0027-5107(76)90044-0;
RA   de Weerd-Kastelein E.A., Keijzer W., Sabour M., Parrington J.M.,
RA   Bootsma D.;
RT   "A xeroderma pigmentosum patient having a high residual activity of
RT   unscheduled DNA synthesis after UV is assigned to complementation
RT   group A.";
RL   Mutat. Res. 37:307-312(1976).
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RX   PubMed=1372102; DOI=10.1016/0921-8777(92)90080-M;
RA   Satokata I., Tanaka K., Miura N., Narita M., Mimaki T., Satoh Y.,
RA   Kondo S., Okada Y.;
RT   "Three nonsense mutations responsible for group A xeroderma
RT   pigmentosum.";
RL   Mutat. Res. 273:193-202(1992).
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RX   PubMed=1702221; DOI=10.1073/pnas.87.24.9908; PMCID=PMC55283;
RA   Satokata I., Tanaka K., Miura N., Miyamoto I., Satoh Y., Kondo S.,
RA   Okada Y.;
RT   "Characterization of a splicing mutation in group A xeroderma
RT   pigmentosum.";
RL   Proc. Natl. Acad. Sci. U.S.A. 87:9908-9912(1990).
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RX   PubMed=2065254; DOI=10.1093/brain/114.3.1335;
RA   Robbins J.H., Brumback R.A., Mendiones M., Barrett S.F., Carl J.R.,
RA   Cho S., Denckla M.B., Ganges M.B., Gerber L.H., Guthrie R.A., Meer J.,
RA   Moshell A.N., Polinsky R.J., Ravin P.D., Sonies B.C., Tarone R.E.;
RT   "Neurological disease in xeroderma pigmentosum. Documentation of a
RT   late onset type of the juvenile onset form.";
RL   Brain 114:1335-1361(1991).
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RX   PubMed=3724780; DOI=10.1016/0167-8817(86)90043-x;
RA   Kantor G.J., Player A.N.;
RT   "A further definition of characteristics of DNA-excision repair in
RT   xeroderma pigmentosum complementation group A strains.";
RL   Mutat. Res. 166:79-88(1986).
//