Cellosaurus iWS229 (CVCL_EQ35)
| Cell line name | iWS229 | |||
|---|---|---|---|---|
| Synonyms | WS iPSC from AG05229 | |||
| Accession | CVCL_EQ35 | |||
| Resource Identification Initiative | To cite this cell line use: iWS229 (RRID:CVCL_EQ35) | |||
| Comments | Population: Japanese. Omics: Transcriptome analysis by microarray. Derived from site: In situ; Thigh, skin; UBERON=UBERON_0004262. 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) | |||
| Hierarchy | Parent: CVCL_X835 (AG05229) Children:
| |||
| Sex of cell | Male | |||
| Age at sampling | 25Y | |||
| Category | Induced pluripotent stem cell | |||
| Publications | PubMed=24749076; DOI=10.1016/j.stemcr.2014.02.006; PMCID=PMC3986587 | |||
| Cross-references | ||||
| Encyclopedic resources | Wikidata; Q54898384 | |||
| Gene expression databases | GEO; GSM1184284
GEO; GSM1184285 | |||
| Entry history | ||||
| Entry creation | 26-Sep-2016 | |||
| Last entry update | 29-Jun-2023 | |||
| Version number | 8 | |||