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Cellosaurus GM09405 (CVCL_UR82)

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Cell line name GM09405
Accession CVCL_UR82
Resource Identification Initiative To cite this cell line use: GM09405 (RRID:CVCL_UR82)
Comments Cell type: Fibroblast; CL=CL_0000057.
Disease Neuronal ceroid lipofuscinosis type 1 (NCIt: C85861)
Congenital neuronal ceroid lipofuscinosis (ORDO: Orphanet_168486)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 16Y
Category Finite cell line
Publications

CLPUB00447
Richard A. Mulivor, Sharon F. Suchy;
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)

PubMed=9247083; DOI=10.1016/S0925-4439(97)00033-1
Linda A. Verkruyse, Marvin R. Natowicz, Sandra L. Hofmann;
Palmitoyl-protein thioesterase deficiency in fibroblasts of individuals with infantile neuronal ceroid lipofuscinosis and I-cell disease.
Biochim. Biophys. Acta 1361:1-5(1997)

Cross-references
Cell line collections (Providers) Coriell; GM09405 - Discontinued
Encyclopedic resources Wikidata; Q93803387
Entry history
Entry creation25-Feb-2019
Last entry update10-Sep-2024
Version number7