| 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
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) Institute for Medical Research (Camden, N.J.); pp.1-171; National Institutes of Health; Bethesda (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) Institute for Medical Research (Camden, N.J.) NIH 87-2011; pp.1-549; National Institutes of Health; Bethesda (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) Institute for Medical Research (Camden, N.J.) NIH 92-2011; pp.1-918; National Institutes of Health; Bethesda (1992) |
|---|
| Cross-references |
|---|
| Cell line collections (Providers) |
Coriell; GM00057
|
|---|
| Cell line databases/resources |
CLO; CLO_0025161
|
|---|
| Encyclopedic resources |
Wikidata; Q54836008
|
|---|
| Entry history |
|---|
| Entry creation | 22-Sep-2015 |
|---|
| Last entry update | 29-Jun-2023 |
|---|
| Version number | 10 |
|---|
