ID   XPKABE
AC   CVCL_U793
SY   Te Ger
DR   ATCC; CRL-1275
DR   Wikidata; Q54972004
RX   PubMed=273925;
RX   PubMed=1372108;
CC   Discontinued: ATCC; CRL-1275; true.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C3967; Xeroderma pigmentosum, complementation group D
DI   ORDO; Orphanet_910; Xeroderma pigmentosum
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   9Y
CA   Finite cell line
DT   Created: 16-04-14; Last updated: 29-06-23; Version: 10
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RX   PubMed=1372108; DOI=10.1016/0921-8777(92)90072-b;
RA   Johnson, Robert T.
RA   Squires, Shoshana
RT   "The XPD complementation group. Insights into xeroderma pigmentosum,
RT   Cockayne's syndrome and trichothiodystrophy.";
RL   Mutat. Res. 273:97-118(1992).
//
RX   PubMed=273925; DOI=10.1073/pnas.75.4.1984; PMCID=PMC392467;
RA   Andrews, Alan D.
RA   Barrett, Susanna F.
RA   Robbins, Jay 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).
//