ID   WS1
AC   CVCL_2766
SY   WS-1; WT-Fibr2
DR   CLO; CLO_0009634
DR   CLDB; cl4732
DR   ATCC; CRL-1502
DR   BioSample; SAMN03471371
DR   BCRC; 60300
DR   CLS; 300344
DR   ECACC; 88021104
DR   GEO; GSM1053952
DR   GEO; GSM1053953
DR   GEO; GSM1053954
DR   GEO; GSM1053979
DR   GEO; GSM1053980
DR   GEO; GSM1053981
DR   Wikidata; Q54994419
RX   PubMed=721103;
RX   PubMed=1383811;
RX   PubMed=3724780;
RX   PubMed=23225669;
CC   Population: African American.
CC   Senescence: Senesces at 67 PDL (ATCC=CRL-1502).
CC   Omics: Transcriptome analysis by microarray.
CC   Discontinued: CLS; 300344; true.
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): ATCC; ECACC
ST   Amelogenin: X
ST   CSF1PO: 10,13
ST   D13S317: 12
ST   D16S539: 10,11
ST   D18S51: 15,19
ST   D19S433: 11,14
ST   D21S11: 28,29
ST   D2S1338: 19
ST   D3S1358: 15,17
ST   D5S818: 13
ST   D7S820: 9,10
ST   D8S1179: 12,13
ST   FGA: 22,27
ST   Penta D: 12
ST   Penta E: 11,12
ST   TH01: 8,10
ST   TPOX: 8,9
ST   vWA: 17,18
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   12FW
CA   Finite cell line
DT   Created: 04-04-12; Last updated: 05-10-23; Version: 19
//
RX   PubMed=721103; DOI=10.1007/BF02617973;
RA   Corfield V.A., Hay R.J.;
RT   "Effects of cystine or glutamine restriction on human diploid
RT   fibroblasts in culture.";
RL   In Vitro 14:787-794(1978).
//
RX   PubMed=1383811; DOI=10.1016/0921-8777(92)90008-Q;
RA   Kantor G.J., Shanower G.A.;
RT   "A re-examination of the intragenome distribution of repaired sites in
RT   proliferating xeroderma pigmentosum complementation group C
RT   fibroblasts.";
RL   Mutat. Res. 293:55-64(1992).
//
RX   PubMed=3724780; DOI=10.1016/0167-8817(86)90043-x;
RA   Kantor G.J., Player A.N.;
RT   "A further definition of characteristics of DNA-excision repair in
RT   xeroderma pigmentosum complementation group A strains.";
RL   Mutat. Res. 166:79-88(1986).
//
RX   PubMed=23225669; DOI=10.1002/stem.1297;
RA   Briggs J.A., Sun J., Shepherd J., Ovchinnikov D.A., Chung T.-L.,
RA   Nayler S.P., Kao L.-P., Morrow C.A., Thakar N.Y., Soo S.-Y., Peura T.T.,
RA   Grimmond S.M., Wolvetang E.J.;
RT   "Integration-free induced pluripotent stem cells model genetic and
RT   neural developmental features of Down syndrome etiology.";
RL   Stem Cells 31:467-478(2013).
//