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Cellosaurus GM07492 iPSC (CVCL_E4CL)

[Text version]
Cell line name GM07492 iPSC
Accession CVCL_E4CL
Resource Identification Initiative To cite this cell line use: GM07492 iPSC (RRID:CVCL_E4CL)
Comments Population: Caucasian.
Caution: Some publication, such as PubMed=36202854, term this cell line just "GM07492" which is wrong as this is the name of the parent cell line.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_7467 (GM07492)
Children:
CVCL_E4CM (GM07492 iPSC GRIN2B LOF)CVCL_E4CN (GM07492 iPSC GRIN2B RD)
Sex of cell Male
Age at sampling 17Y
Category Induced pluripotent stem cell
Publications

PubMed=29937144; DOI=10.1016/j.stemcr.2018.05.018; PMCID=PMC6067152
Bell S., Maussion G., Jefri M., Peng H.-S., Theroux J.-F., Silveira H.B., Soubannier V., Wu H.-R., Hu P., Galat E., Torres-Platas S.G., Boudreau-Pinsonneault C., O'Leary L.A., Galat V., Turecki G., Durcan T.M., Fon E.A., Mechawar N., Ernst C.
Disruption of GRIN2B impairs differentiation in human neurons.
Stem Cell Reports 11:183-196(2018)

PubMed=36202854; DOI=10.1038/s41467-022-33364-z; PMCID=PMC9537523
Wang Y.-Q., Chiola S., Yang G., Russell C., Armstrong C.J., Wu Y.-Y., Spampanato J.G., Tarboton P., Ullah H.M.A., Edgar N.U., Chang A.N., Harmin D.A., Bocchi V.D., Vezzoli E., Besusso D., Cui J., Cattaneo E., Kubanek J., Shcheglovitov A.
Modeling human telencephalic development and autism-associated SHANK3 deficiency using organoids generated from single neural rosettes.
Nat. Commun. 13:5688.1-5688.25(2022)

Entry history
Entry creation19-Dec-2024
Last entry update19-Dec-2024
Version number1