Cellosaurus HEL100.1 (CVCL_VT43)
| Cell line name | HEL100.1 |
|---|---|
| Accession | CVCL_VT43 |
| Resource Identification Initiative | To cite this cell line use: HEL100.1 (RRID:CVCL_VT43) |
| Comments | From: University of Helsinki; Helsinki; Finland. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Sequence variations |
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| Disease | Fragile X syndrome (NCIt: C84717) Fragile X syndrome (ORDO: Orphanet_908) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_VT44 ! HEL100.2 |
| Sex of cell | Male |
| Age at sampling | Children |
| Category | Induced pluripotent stem cell |
| Publications | PubMed=27411166; DOI=10.1002/dneu.22419 PubMed=29339535; DOI=10.1126/scisignal.aan8784 PubMed=30503263; DOI=10.1016/j.stemcr.2018.11.003; PMCID=PMC6294261 |
| Cross-references | |
| Encyclopedic resources | Wikidata; Q94096114 |
| Entry history | |
| Entry creation | 24-May-2019 |
| Last entry update | 19-Dec-2024 |
| Version number | 10 |