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Cellosaurus WS11KO (CVCL_A7PI)

[Text version]
Cell line name WS11KO
Synonyms Werner Syndrome 11 KObe
Accession CVCL_A7PI
Resource Identification Initiative To cite this cell line use: WS11KO (RRID:CVCL_A7PI)
Comments Population: Japanese.
Senescence: Senesces at 26 PDL (PubMed=4083160).
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Werner syndrome (NCIt: C3447)
Werner syndrome (ORDO: Orphanet_902)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 37Y
Category Finite cell line
Publications

PubMed=4083156; DOI=10.1007/978-1-4684-7853-2_17
Tanaka K., Yamamura K.-i., Fukuchi K., Kawai K., Kumahara Y.
Cell fusion studies in the Werner syndrome.
Adv. Exp. Med. Biol. 190:341-351(1985)

PubMed=4083160; DOI=10.1007/978-1-4684-7853-2_23
Fujiwara Y., Kano Y., Ichihashi M., Nakao Y., Matsumura T.
Abnormal fibroblast aging and DNA replication in the Werner syndrome.
Adv. Exp. Med. Biol. 190:459-477(1985)

Cross-references
Encyclopedic resources Wikidata; Q107117509
Entry history
Entry creation20-May-2021
Last entry update29-Jun-2023
Version number6