ID   CS1OS
AC   CVCL_M678
SY   Cockayne Syndrome 1 OSaka
DR   JCRB; KURB1906
DR   Wikidata; Q54814531
RX   PubMed=7151298;
RX   PubMed=9777763;
CC   Population: Japanese.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C135725; Cockayne syndrome type A
DI   ORDO; Orphanet_191; Cockayne syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
CA   Finite cell line
DT   Created: 05-11-13; Last updated: 29-06-23; Version: 10
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RX   PubMed=7151298; DOI=10.1111/j.1399-0004.1982.tb01424.x;
RA   Sugita, Takahiro
RA   Ikenaga, Mituo
RA   Suehara, Noriyuki
RA   Kozuka, Takehito
RA   Furuyama, Jun-ichi
RA   Yabuuchi, Hyakuji
RT   "Prenatal diagnosis of Cockayne syndrome using assay of colony-forming
RT   ability in ultraviolet light irradiated cells.";
RL   Clin. Genet. 22:137-142(1982).
//
RX   PubMed=9777763; DOI=10.1016/S0190-9622(98)70005-2;
RA   Miyauchi-Hashimoto, Hiroko
RA   Akaeda, Tamiyo
RA   Maihara, Toshiro
RA   Ikenaga, Mituo
RA   Horio, Takeshi
RT   "Cockayne syndrome without typical clinical manifestations including
RT   neurologic abnormalities.";
RL   J. Am. Acad. Dermatol. 39:565-570(1998).
//