ID   AG08805
AC   CVCL_0N72
SY   AG8805
DR   CLO; CLO_0031383
DR   Coriell; AG08805
DR   Wikidata; Q54742533
RX   CelloPub=CLPUB00597;
RX   PubMed=8823375;
RX   PubMed=9447232;
CC   Population: Caucasian.
CC   Derived from site: In situ; Arm, skin; UBERON=UBERON_0002427.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_0N71 ! AG08804
SX   Female
AG   37Y
CA   Finite cell line
DT   Created: 10-04-15; Last updated: 29-06-23; Version: 10
//
RX   PubMed=8823375; DOI=10.1111/1523-1747.ep12584287;
RA   Moriwaki, Shin-ichi
RA   Stefanini, Miria
RA   Lehmann, Alan Robert
RA   Hoeijmakers, Jan Hendrik Jozef
RA   Robbins, Jay H.
RA   Rapin, Isabelle
RA   Botta, Elena
RA   Tanganelli, Bianca
RA   Vermeulen, Wim
RA   Broughton, Bernard C.
RA   Kraemer, Kenneth H.
RT   "DNA repair and ultraviolet mutagenesis in cells from a new patient
RT   with xeroderma pigmentosum group G and Cockayne syndrome resemble
RT   xeroderma pigmentosum cells.";
RL   J. Invest. Dermatol. 107:647-653(1996).
//
RX   PubMed=9447232; DOI=10.1016/S0921-8777(97)00031-1;
RA   Okinaka, Richard T.
RA   Perez-Castro, Ana V.
RA   Sena, Anthony
RA   Laubscher, Kevin
RA   Strniste, Gary F.
RA   Park, Min S.
RA   Hernandez, Rudy
RA   MacInnes, Mark A.
RA   Kraemer, Kenneth H.
RT   "Heritable genetic alterations in a xeroderma pigmentosum group
RT   G/Cockayne syndrome pedigree.";
RL   Mutat. Res. 385:107-114(1997).
//
RX   CelloPub=CLPUB00597;
RG   National Institute on Aging;
RT   "1994 catalog of cell lines. NIA Aging Cell Repository.";
RL   (In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-351; National Institutes of Health; Bethesda; USA (1994).
//