ID   XP59TO
AC   CVCL_ZM30
SY   Xeroderma Pigmentosum 59 TOkyo
DR   JCRB; KURB1078
DR   Wikidata; Q98135967
RX   PubMed=3341805;
RX   PubMed=3922833;
RX   PubMed=4031543;
CC   Population: Japanese.
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   6Y
CA   Finite cell line
DT   Created: 02-07-20; Last updated: 10-04-25; Version: 6
//
RX   PubMed=3922833; DOI=10.20772/cancersci1985.76.3_162;
RA   Fujiwara, Yoshisada
RA   Satoh, Yoshiaki
RT   "Assignment of two Japanese xeroderma pigmentosum patients to
RT   complementation group D and their characteristics.";
RL   Jpn. J. Cancer Res. 76:162-166(1985).
//
RX   PubMed=3341805; DOI=10.1001/archderm.1988.01670020074021;
RA   Ichihashi, Masamitsu
RA   Yamamura, Keizo
RA   Hiramoto, Takeaki
RA   Fujiwara, Yoshisada
RT   "No apparent neurologic defect in a patient with xeroderma pigmentosum
RT   complementation group D.";
RL   Arch. Dermatol. 124:256-260(1988).
//
RX   PubMed=4031543; DOI=10.1111/1523-1747.ep12276776;
RA   Ichihashi, Masamitsu
RA   Fujiwara, Yoshisada
RA   Uehara, Yoshihiko
RA   Matsumoto, Akira
RT   "A mild form of xeroderma pigmentosum assigned to complementation
RT   group G and its repair heterogeneity.";
RL   J. Invest. Dermatol. 85:284-287(1985).
//