Cell line name | VUB13_FXS |
---|---|
Synonyms | VUBe012-A |
Accession | CVCL_9849 |
Resource Identification Initiative | To cite this cell line use: VUB13_FXS (RRID:CVCL_9849) |
Comments | From: Vrije Universiteit Brussel; Brussels; Belgium. |
Sequence variations |
|
Disease | Fragile X syndrome (NCIt: C84717) Fragile X syndrome (ORDO: Orphanet_908) |
Species of origin | Homo sapiens (Human)
(NCBI Taxonomy: 9606)
|
Sex of cell | Female |
Age at sampling | Blastocyst stage |
Category | Embryonic stem cell |
Publications | PubMed=20224973; DOI=10.1007/s11626-010-9284-4 PubMed=27690107; DOI=10.3390/genes7100077 |
Cross-references | |
Cell line databases/resources | hPSCreg; VUBe012-A
ISCR; 240 SKIP; SKIP001835 |
Encyclopedic resources | Wikidata; Q54993398 |
Entry history | |
Entry creation | 06-Jun-2012 |
Last entry update | 16-Dec-2021 |
Version number | 15 |