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Cellosaurus Lis03_FXS4 (CVCL_B925)

[Text version]
Cell line name Lis03_FXS4
Synonyms Lis03_FXS_4
Accession CVCL_B925
Resource Identification Initiative To cite this cell line use: Lis03_FXS4 (RRID:CVCL_B925)
Comments From: Tel-Aviv Sourasky Medical Center; Tel-Aviv; Israel.
Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-15-0331.
Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
Cell type: Embryonic stem cell; CL=CL_0002322.
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=20186514; DOI=10.1007/s11626-010-9275-5
Frumkin T., Malcov M., Telias M., Gold V., Schwartz T., Azem F., Amit A., Yaron Y., Ben-Yosef D.
Human embryonic stem cells carrying mutations for severe genetic disorders.
In Vitro Cell. Dev. Biol. Anim. 46:327-336(2010)

PubMed=21585244; DOI=10.1089/scd.2011.0102; PMCID=PMC3272241
Ben-Yosef D., Amit A., Malcov M., Frumkin T., Ben-Yehudah A., Eldar I., Mey-Raz N., Azem F., Altarescu G., Renbaum P., Beeri R., Varshaver I., Eldar-Geva T., Epsztejn-Litman S., Levy-Lahad E., Eiges R.
Female sex bias in human embryonic stem cell lines.
Stem Cells Dev. 21:363-372(2012)

Cross-references
Cell line databases/resources NIHhESC; NIHhESC-15-0331
Encyclopedic resources Wikidata; Q54902589
Entry history
Entry creation06-Jun-2012
Last entry update19-Dec-2024
Version number20