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Cellosaurus WG1083 (CVCL_UH77)

[Text version]
Cell line name WG1083
Synonyms WG 1083
Accession CVCL_UH77
Resource Identification Initiative To cite this cell line use: WG1083 (RRID:CVCL_UH77)
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 Prolidase deficiency (NCIt: C85029)
Prolidase deficiency (ORDO: Orphanet_742)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling Age unspecified
Category Finite cell line
Publications

CLPUB00453
Boright A.P.
Prolidase deficiency: studies in human dermal fibroblasts.
Thesis PhD (1988); McGill University Montreal; Montreal; Canada

PubMed=2705457; PMCID=PMC1715628
Boright A.P., Scriver C.R., Lancaster G.A., Choy F.Y.-M.
Prolidase deficiency: biochemical classification of alleles.
Am. J. Hum. Genet. 44:731-740(1989)

Cross-references
Encyclopedic resources Wikidata; Q98134885
Entry history
Entry creation25-Feb-2019
Last entry update29-Jun-2023
Version number7