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Cellosaurus STR-I-189-FRAXA (CVCL_C084)

[Text version]
Cell line name STR-I-189-FRAXA
Synonyms STR-189-FRAXA; INSERMe005-A; INSRMe005-A
Accession CVCL_C084
Resource Identification Initiative To cite this cell line use: STR-I-189-FRAXA (RRID:CVCL_C084)
Comments From: INSERM; Paris; France.
Registration: French Agence de la Biomedecine; FE08-065-L1.
Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
Cell type: Embryonic stem cell; CL=CL_0002322.
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
Web pages https://www.agence-biomedecine.fr/IMG/pdf/inserm_str_i_189_fraxa.pdf
Publications

PubMed=20217271; DOI=10.1007/s11626-010-9300-8
Tropel P., Tournois J., Come J., Varela C., Moutou C., Fragner P., Cailleret M., Laabi Y., Peschanski M., Viville S.
High-efficiency derivation of human embryonic stem cell lines following pre-implantation genetic diagnosis.
In Vitro Cell. Dev. Biol. Anim. 46:376-385(2010)

PubMed=27690107; DOI=10.3390/genes7100077; PMCID=PMC5083916
Mor-Shaked H., Eiges R.
Modeling fragile X syndrome using human pluripotent stem cells.
Genes (Basel) 7:77.1-77.19(2016)

Cross-references
Cell line databases/resources hPSCreg; INSRMe005-A
SKIP; SKIP002319
Encyclopedic resources Wikidata; Q54970610
Entry history
Entry creation06-Jun-2012
Last entry update10-Sep-2024
Version number15