ID   XPHM4LO
AC   CVCL_WY88
SY   Xeroderma Pigmentosum Heterozygote Mother 4 LOndon
DR   Wikidata; Q98136338
RX   DOI=10.1007/978-1-4757-1117-2_12;
RX   PubMed=6947227;
CC   Sequence variation: Mutation; HGNC; HGNC:12814; XPA; Simple; c.468_469delAA; Zygosity=Heterozygous (from familial inference of XP4LO).
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   Adult
CA   Finite cell line
DT   Created: 06-09-19; Last updated: 19-12-24; Version: 9
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RX   DOI=10.1007/978-1-4757-1117-2_12;
RA   Arlett C.F., Harcourt S.A.;
RT   "The mutagen sensitivity response of cells from individuals
RT   heterozygous for DNA repair deficiency genes.";
RL   (In book chapter) The use of human cells for the evaluation of risk from physical and chemical agents; Castellani A. (eds.); pp.155-167; Springer; Boston; USA (1983).
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RX   PubMed=6947227; DOI=10.1073/pnas.78.10.6236; PMCID=PMC349013;
RA   Miskin R., Ben-Ishai R.;
RT   "Induction of plasminogen activator by UV light in normal and
RT   xeroderma pigmentosum fibroblasts.";
RL   Proc. Natl. Acad. Sci. U.S.A. 78:6236-6240(1981).
//