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Cellosaurus GM1-1019 (CVCL_C0NX)

[Text version]
Cell line name GM1-1019
Accession CVCL_C0NX
Resource Identification Initiative To cite this cell line use: GM1-1019 (RRID:CVCL_C0NX)
Comments Population: Japanese.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease GM1 gangliosidosis (NCIt: C84739)
GM1 gangliosidosis (ORDO: Orphanet_354)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_C0NY (GM1-1019-SV)
Sex of cell Sex unspecified
Age at sampling Age unspecified
Category Finite cell line
Publications

PubMed=2990594; DOI=10.1007/BF01119596
Momoi T., Furuya T., Suzuki Y., Sato H., Yamaguchi N.
In vitro establishment of human fibroblasts of lysosomal diseases, GM1-gangliosidosis and Sandhoff disease, by transformation with origin-minus SV40 DNA.
Biosci. Rep. 5:267-273(1985)

PubMed=3027449; DOI=10.1007/BF01819299
Furuya T., Momoi T., Suzuki Y., Sato H., Yamaguchi N.
Establishment of human fibroblast cell lines with lysosomal enzyme deficiency by transformation with origin-minus SV40 DNA.
J. Inherit. Metab. Dis. 8:143-144(1985)

Cross-references
Encyclopedic resources Wikidata; Q112929586
Entry history
Entry creation23-Jun-2022
Last entry update19-Dec-2024
Version number7