ID   XP6KO
AC   CVCL_ZM31
SY   Xeroderma Pigmentosum 6 KObe
DR   Wikidata; Q98136045
RX   PubMed=3341805;
RX   PubMed=3922833;
RX   PubMed=4011712;
RX   PubMed=4031543;
RX   PubMed=7259973;
RX   PubMed=7300843;
CC   Population: Japanese.
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   Male
AG   3Y
CA   Finite cell line
DT   Created: 02-07-20; Last updated: 29-06-23; Version: 5
//
RX   PubMed=3341805; DOI=10.1001/archderm.1988.01670020074021;
RA   Ichihashi M., Yamamura K., Hiramoto T., Fujiwara Y.;
RT   "No apparent neurologic defect in a patient with xeroderma pigmentosum
RT   complementation group D.";
RL   Arch. Dermatol. 124:256-260(1988).
//
RX   PubMed=3922833; DOI=10.20772/cancersci1985.76.3_162;
RA   Fujiwara Y., Satoh Y.;
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=4011712; DOI=10.1111/j.1751-1097.1985.tb03538.x;
RA   Fujiwara Y., Uehara Y., Ichihashi M., Nishioka K.;
RT   "Xeroderma pigmentosum complementation group F: more assignments and
RT   repair characteristics.";
RL   Photochem. Photobiol. 41:629-634(1985).
//
RX   PubMed=4031543; DOI=10.1111/1523-1747.ep12276776;
RA   Ichihashi M., Fujiwara Y., Uehara Y., Matsumoto A.;
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).
//
RX   PubMed=7259973; DOI=10.1111/j.1365-2133.1981.tb00876.x;
RA   Ichihashi M., Fujiwara Y.;
RT   "Clinical and photobiological characteristics of Japanese xeroderma
RT   pigmentosum variant.";
RL   Br. J. Dermatol. 105:1-12(1981).
//
RX   PubMed=7300843; DOI=10.1016/0027-5107(81)90123-8;
RA   Kano Y., Fujiwara Y.;
RT   "Roles of DNA interstrand crosslinking and its repair in the induction
RT   of sister-chromatid exchange and a higher induction in Fanconi's
RT   anemia cells.";
RL   Mutat. Res. 81:365-375(1981).
//