ID   PSV811
AC   CVCL_3142
SY   PSV 811; AG07066; AG07066B
DR   CLO; CLO_0035650
DR   BioSample; SAMN03152041
DR   BioSample; SAMN03471630
DR   Coriell; AG07066
DR   JCRB; JCRB0604
DR   RCB; RCB0223
DR   Wikidata; Q54948617
RX   CelloPub=CLPUB00597;
RX   PubMed=2762303;
RX   PubMed=3002148;
RX   PubMed=9230208;
RX   PubMed=20143388;
WW   https://cellbank.nibiohn.go.jp/legacy/cellbank/qualitycontrol/identification/summary.htm
WW   https://iclac.org/wp-content/uploads/Cross-Contaminations_v12_distribution.xlsx
CC   Problematic cell line: Contaminated. Shown to be a WI-38 derivative (PubMed=20143388). Originally thought to originate from the skin fibroblasts of a 29 year old female patient with Werner syndrome.
CC   Registration: International Cell Line Authentication Committee, Register of Misidentified Cell Lines; ICLAC-00343.
CC   Population: Caucasian; Swedish.
CC   Discontinued: RCB; RCB0223; true.
CC   Derived from site: In situ; Fetal lung; UBERON=UBERON_0005597.
CC   Cell type: Fibroblast of lung; CL=CL_0002553.
ST   Source(s): JCRB
ST   Amelogenin: X
ST   CSF1PO: 10,12
ST   D13S317: 11
ST   D16S539: 11,12
ST   D5S818: 10
ST   D7S820: 9,11
ST   TH01: 9.3
ST   TPOX: 8
ST   vWA: 20
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_0579 ! WI-38
SX   Female
AG   16FW
CA   Finite cell line
DT   Created: 04-04-12; Last updated: 29-06-23; Version: 26
//
RX   CelloPub=CLPUB00597;
RG   National Institute on Aging;
RT   "1994 catalog of cell lines. NIA Aging Cell Repository.";
RL   (In) Institute for Medical Research (Camden, N.J.); pp.1-351; National Institutes of Health; Bethesda (1994).
//
RX   PubMed=2762303; DOI=10.1073/pnas.86.15.5893;
RA   Fukuchi K.-i., Martin G.M., Monnat R.J. Jr.;
RT   "Mutator phenotype of Werner syndrome is characterized by extensive
RT   deletions.";
RL   Proc. Natl. Acad. Sci. U.S.A. 86:5893-5897(1989).
//
RX   PubMed=3002148; DOI=10.1007/978-1-4684-7853-2_15;
RA   Matsumura T., Nagata M., Konishi R., Goto M.;
RT   "Studies of SV40-infected Werner syndrome fibroblasts.";
RL   Adv. Exp. Med. Biol. 190:313-330(1985).
//
RX   PubMed=9230208;
RA   Bennett S.E., Umar A., Oshima J., Monnat R.J. Jr., Kunkel T.A.;
RT   "Mismatch repair in extracts of Werner syndrome cell lines.";
RL   Cancer Res. 57:2956-2960(1997).
//
RX   PubMed=20143388; DOI=10.1002/ijc.25242;
RA   Capes-Davis A., Theodosopoulos G., Atkin I., Drexler H.G., Kohara A.,
RA   MacLeod R.A.F., Masters J.R.W., Nakamura Y., Reid Y.A., Reddel R.R.,
RA   Freshney R.I.;
RT   "Check your cultures! A list of cross-contaminated or misidentified
RT   cell lines.";
RL   Int. J. Cancer 127:1-8(2010).
//