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Cellosaurus CS1OS (CVCL_M678)

[Text version]
Cell line name CS1OS
Synonyms Cockayne Syndrome 1 OSaka
Accession CVCL_M678
Resource Identification Initiative To cite this cell line use: CS1OS (RRID:CVCL_M678)
Comments Population: Japanese.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Cockayne syndrome type A (NCIt: C135725)
Cockayne syndrome (ORDO: Orphanet_191)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Category Finite cell line
Publications

PubMed=7151298; DOI=10.1111/j.1399-0004.1982.tb01424.x
Takahiro Sugita, Mituo Ikenaga, Noriyuki Suehara, Takehito Kozuka, Jun-ichi Furuyama, Hyakuji Yabuuchi;
Prenatal diagnosis of Cockayne syndrome using assay of colony-forming ability in ultraviolet light irradiated cells.
Clin. Genet. 22:137-142(1982)

PubMed=9777763; DOI=10.1016/S0190-9622(98)70005-2
Hiroko Miyauchi-Hashimoto, Tamiyo Akaeda, Toshiro Maihara, Mituo Ikenaga, Takeshi Horio;
Cockayne syndrome without typical clinical manifestations including neurologic abnormalities.
J. Am. Acad. Dermatol. 39:565-570(1998)

Cross-references
Cell line collections (Providers) JCRB; KURB1906
Encyclopedic resources Wikidata; Q54814531
Entry history
Entry creation05-Nov-2013
Last entry update29-Jun-2023
Version number10