ID   GM01176
AC   CVCL_X241
SY   GM-1176; GM 1176; GM01176A; TS2 fibroblast
DR   CLO; CLO_0030203
DR   BioSample; SAMN00803686
DR   Coriell; GM01176
DR   Wikidata; Q54836686
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=6661932;
RX   PubMed=21949351;
CC   Population: Caucasian.
CC   Karyotypic information: 45,X[18].arr(X)x1 (Coriell=GM01176).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C26900; Turner syndrome
DI   ORDO; Orphanet_881; Turner syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   8Y
CA   Finite cell line
DT   Created: 17-07-14; Last updated: 02-05-24; Version: 14
//
RX   CelloPub=CLPUB00447;
RA   Mulivor R.A., Suchy S.F.;
RT   "1992/1993 catalog of cell lines. NIGMS human genetic mutant cell
RT   repository. 16th edition. October 1992.";
RL   (In) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992).
//
RX   DOI=10.5962/bhl.title.4090;
RA   Coriell L.L., Greene A.E.;
RT   "The human genetic mutant cell repository: list of genetic variants,
RT   chromosomal aberrations and normal cell cultures submitted to the
RT   repository. 4th edition. October 1977.";
RL   (In) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda (1977).
//
RX   PubMed=6661932; DOI=10.1159/000131990;
RA   Aronson M.M., Nichols W.W., Mulivor R.A., Greene A.E., Coriell L.L.;
RT   "Chromosome maps of cell lines with specific monosomic or trisomic
RT   portions of the genome in the NIGMS Human Genetic Mutant Cell
RT   Repository.";
RL   Cytogenet. Cell Genet. 36:652-658(1983).
//
RX   PubMed=21949351; DOI=10.1093/hmg/ddr435;
RA   Li W., Wang X.-M., Fan W.-X., Zhao P., Chan Y.-C., Chen S.,
RA   Zhang S.-Q., Guo X.-P., Zhang Y., Li Y.-H., Cai J.-L., Qin D.-J.,
RA   Li X.-Y., Yang J.-Y., Peng T.-R., Zychlinski D., Hoffmann D.,
RA   Zhang R.-S., Deng K., Ng K.-M., Menten B., Zhong M., Wu J.-Y., Li Z.-Y.,
RA   Chen Y.-L., Schambach A., Tse H.-F., Pei D.-Q., Esteban M.A.;
RT   "Modeling abnormal early development with induced pluripotent stem
RT   cells from aneuploid syndromes.";
RL   Hum. Mol. Genet. 21:32-45(2012).
//