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Cellosaurus WG0738 (CVCL_UH69)

[Text version]
Cell line name WG0738
Synonyms WG 738
Accession CVCL_UH69
Resource Identification Initiative To cite this cell line use: WG0738 (RRID:CVCL_UH69)
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 Arakawa syndrome II (NCIt: C99081)
Methylcobalamin deficiency type cblG (ORDO: Orphanet_2170)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 6M
Category Finite cell line
Publications

CLPUB00452
Buchanan J.A.
Fibroblast plasma membrane vesicles to study inborn errors of transport.
Thesis PhD (1984); McGill University Montreal; Montreal; Canada

PubMed=3937470; DOI=10.1111/j.1749-6632.1985.tb14891.x
Buchanan J.A., Rosenblatt D.S., Scriver C.R.
Cultured human fibroblasts and plasma membrane vesicles to investigate transport function and the effects of genetic mutation.
Ann. N. Y. Acad. Sci. 456:401-403(1985)

Cross-references
Encyclopedic resources Wikidata; Q98134860
Entry history
Entry creation25-Feb-2019
Last entry update29-Jun-2023
Version number7