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Cellosaurus Lis26_FXS6 (CVCL_Y352)

[Text version]
Cell line name Lis26_FXS6
Synonyms Lis26_FXS_6
Accession CVCL_Y352
Resource Identification Initiative To cite this cell line use: Lis26_FXS6 (RRID:CVCL_Y352)
Comments From: Tel-Aviv Sourasky Medical Center; Tel-Aviv; Israel.
Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-15-0350.
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 Male
Age at sampling Blastocyst stage
Category Embryonic stem cell
Publications

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 NIHhESC; NIHhESC-15-0350
Encyclopedic resources Wikidata; Q54902612
Entry history
Entry creation07-Nov-2014
Last entry update19-Dec-2024
Version number14