| Cell line name | CS1MO |
|---|---|
| Synonyms | Cockayne Syndrome 1 MOriguchi |
| Accession | CVCL_ZP14 |
| Resource Identification Initiative | To cite this cell line use: CS1MO (RRID:CVCL_ZP14) |
| Comments | Population: Japanese. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Disease | Cockayne syndrome type B (NCIt: C135726) Cockayne syndrome (ORDO: Orphanet_191) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Female |
| Age at sampling | Children |
| Category | Finite cell line |
| Publications | PubMed=9777763; DOI=10.1016/s0190-9622(98)70005-2 |
| Cross-references | |
| Cell line collections (Providers) | JCRB; KURB1885
JCRB; KURB1886 |
| Encyclopedic resources | Wikidata; Q98125731 |
| Entry history | |
| Entry creation | 02-Jul-2020 |
| Last entry update | 29-Jun-2023 |
| Version number | 5 |