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Cellosaurus WG0139 (CVCL_UD62)

[Text version]
Cell line name WG0139
Synonyms WG 139; WG139
Accession CVCL_UD62
Resource Identification Initiative To cite this cell line use: WG0139 (RRID:CVCL_UD62)
Comments From: Montreal Children's Hospital cell repository; Montreal; Canada.
Miscellaneous: Cell line no longer available.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Giant axonal neuropathy (NCIt: C84728)
Giant axonal neuropathy (ORDO: Orphanet_643)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling Children
Category Finite cell line
Publications

PubMed=6280044; DOI=10.1002/mus.880050215
Pena S.D.J.
Giant axonal neuropathy: an inborn error of organization of intermediate filaments.
Muscle Nerve 5:166-172(1982)

PubMed=6315439
Pena S.D.J., Opas M., Turksen K., Kalnins V.I., Carpenter S.H.
Immunocytochemical studies of intermediate filament aggregates and their relationship to microtubules in cultured skin fibroblasts from patients with giant axonal neuropathy.
Eur. J. Cell Biol. 31:227-234(1983)

PubMed=3880753; DOI=10.1083/jcb.100.1.245; PMCID=PMC2113460
Klymkowsky M.W., Plummer D.J.
Giant axonal neuropathy: a conditional mutation affecting cytoskeletal organization.
J. Cell Biol. 100:245-250(1985)

Cross-references
Encyclopedic resources Wikidata; Q98134827
Entry history
Entry creation13-Nov-2018
Last entry update29-Jun-2023
Version number7