ID   TS-495
AC   CVCL_B5PX
DR   Wikidata; Q112041864
RX   PubMed=36611;
RX   PubMed=559490;
RX   PubMed=817596;
CC   Population: Jewish; Ashkenazi.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C85184; Tay-Sachs disease
DI   ORDO; Orphanet_845; Tay-Sachs disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
CA   Finite cell line
DT   Created: 17-03-22; Last updated: 29-06-23; Version: 4
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RX   PubMed=36611; DOI=10.1073/pnas.76.4.1957; PMCID=PMC383512;
RA   DeLuca C., Brown J.A., Shows T.B.;
RT   "Lysosomal arylsulfatase deficiencies in humans: chromosome
RT   assignments for arylsulfatase A and B.";
RL   Proc. Natl. Acad. Sci. U.S.A. 76:1957-1961(1979).
//
RX   PubMed=559490; DOI=10.1007/BF00484467;
RA   Lalley P.A., Brown J.A., Eddy R.L., Haley L.L., Byers M.G.,
RA   Goggin A.P., Shows T.B.;
RT   "Human beta-glucuronidase: assignment of the structural gene to
RT   chromosome 7 using somatic cell hybrids.";
RL   Biochem. Genet. 15:367-382(1977).
//
RX   PubMed=817596; PMCID=PMC1684927;
RA   Rattazzi M.C., Brown J.A., Davidson R.G., Shows T.B.;
RT   "Studies on complementation of beta hexosaminidase deficiency in human
RT   GM2 gangliosidosis.";
RL   Am. J. Hum. Genet. 28:143-154(1976).
//