Cellosaurus UOMi012-A (CVCL_E5E7)
| Cell line name | UOMi012-A |
|---|---|
| Synonyms | NAAS-hiPSC-Fontan1 |
| Accession | CVCL_E5E7 |
| Resource Identification Initiative | To cite this cell line use: UOMi012-A (RRID:CVCL_E5E7) |
| Comments | From: University of Manitoba; Winnipeg; Canada. Donor information: Established from a patient that who went through the surgical procedure for Fontan circulation at the age of 13 (PubMed=39089181). Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Disease | Congenital heart disease (NCIt: C95834) Rare syndrome with cardiac malformations (ORDO: Orphanet_156532) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Female |
| Age at sampling | 38Y |
| Category | Induced pluripotent stem cell |
| Publications | PubMed=39089181; DOI=10.1016/j.scr.2024.103509 |
| Cross-references | |
| Cell line databases/resources | hPSCreg; UOMi012-A |
| Biological sample resources | BioSamples; SAMEA115296781 |
| Entry history | |
| Entry creation | 19-Dec-2024 |
| Last entry update | 19-Dec-2024 |
| Version number | 1 |