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Cellosaurus WG0699 (CVCL_UH68)

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Cell line name WG0699
Synonyms WG 699
Accession CVCL_UH68
Resource Identification Initiative To cite this cell line use: WG0699 (RRID:CVCL_UH68)
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 Hereditary folate malabsorption (NCIt: C156424)
Hereditary folate malabsorption (ORDO: Orphanet_90045)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 40Y
Category Finite cell line
Publications

CLPUB00452
Janet A. Buchanan;
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
Janet A. Buchanan, David S. Rosenblatt, Charles Robert Scriver;
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; Q98134854
Entry history
Entry creation25-Feb-2019
Last entry update29-Jun-2023
Version number7