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Cellosaurus GM00057 (CVCL_2N23)

[Text version]
Cell line name GM00057
Synonyms GM-57; GM00057A; GM0057A
Accession CVCL_2N23
Resource Identification Initiative To cite this cell line use: GM00057 (RRID:CVCL_2N23)
Comments Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Propionic acidemia (NCIt: C85030)
Propionic acidemia (ORDO: Orphanet_35)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 6Y
Category Finite cell line
Publications

PubMed=5101292; DOI=10.1172/JCI106466; PMCID=PMC291900
Hsia Y.E., Scully K.J., Rosenberg L.E.
Inherited propionyl-Coa carboxylase deficiency in 'ketotic hyperglycinemia'.
J. Clin. Invest. 50:127-130(1971)

DOI=10.5962/bhl.title.4090
Coriell L.L., Greene A.E.
The human genetic mutant cell repository: list of genetic variants, chromosomal aberrations and normal cell cultures submitted to the repository. 4th edition. October 1977.
(In misc. document) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda; USA (1977)

CLPUB00720
Greene A.E., Mulivor R.A.
1986/1987 catalog of cell lines. NIGMS human genetic mutant cell repository. 13th edition. October 1986.
(In misc. document) Institute for Medical Research (Camden, N.J.) NIH 87-2011; pp.1-549; National Institutes of Health; Bethesda; USA (1986)

CLPUB00447
Mulivor R.A., Suchy S.F.
1992/1993 catalog of cell lines. NIGMS human genetic mutant cell repository. 16th edition. October 1992.
(In misc. document) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda; USA (1992)

Cross-references
Cell line collections (Providers) Coriell; GM00057
Cell line databases/resources CLO; CLO_0025161
Encyclopedic resources Wikidata; Q54836008
Entry history
Entry creation22-Sep-2015
Last entry update29-Jun-2023
Version number10