ID   GM00073
AC   CVCL_H955
SY   GM-73; GM073; GM0073; GM 0073
DR   CLO; CLO_0025163
DR   Coriell; GM00073
DR   Wikidata; Q54836017
RX   CelloPub=CLPUB00447;
RX   DOI=10.5962/bhl.title.4090;
RX   PubMed=4796242;
RX   PubMed=6293786;
RX   PubMed=6947233;
RX   PubMed=10377420;
CC   Population: Caucasian.
CC   Karyotypic information: 46,X,t(X;14)(q13;q32) (PubMed=10377420).
CC   Cell type: Fibroblast; CL=CL_0000057.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_H956 ! GM10073
SX   Female
AG   Adult
CA   Finite cell line
DT   Created: 11-02-13; Last updated: 29-06-23; Version: 13
//
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 misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (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 misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977).
//
RX   PubMed=4796242; DOI=10.1159/000130464;
RA   Opitz J.M., Pallister P.D., Ruddle F.H.;
RT   "An (X;14) translocation, balanced, 46 chromosomes. Repository
RT   identification No. GM-73.";
RL   Cytogenet. Cell Genet. 12:289-290(1973).
//
RX   PubMed=6293786; DOI=10.1002/cyto.990030302;
RA   Lebo R.V.;
RT   "Chromosome sorting and DNA sequence localization.";
RL   Cytometry 3:145-154(1982).
//
RX   PubMed=6947233; DOI=10.1073/pnas.78.10.6339; PMCID=PMC349034;
RA   Migeon B.R., Brown T.R., Axelman J., Migeon C.J.;
RT   "Studies of the locus for androgen receptor: localization on the human
RT   X chromosome and evidence for homology with the Tfm locus in the
RT   mouse.";
RL   Proc. Natl. Acad. Sci. U.S.A. 78:6339-6343(1981).
//
RX   PubMed=10377420; DOI=10.1073/pnas.96.13.7364; PMCID=PMC22091;
RA   Carrel L., Willard H.F.;
RT   "Heterogeneous gene expression from the inactive X chromosome: an
RT   X-linked gene that escapes X inactivation in some human cell lines but
RT   is inactivated in others.";
RL   Proc. Natl. Acad. Sci. U.S.A. 96:7364-7369(1999).
//