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Cellosaurus TS1-iPS-C1 (CVCL_UG64)

[Text version]
Cell line name TS1-iPS-C1
Synonyms TS1-iPS-C1P22
Accession CVCL_UG64
Resource Identification Initiative To cite this cell line use: TS1-iPS-C1 (RRID:CVCL_UG64)
Comments Omics: Transcriptomics; Microarray.
Derived from site: In situ; Amniotic fluid; UBERON=UBERON_0000173.
Cell type: Amniocyte; CL=CL_0002323.
Disease Turner syndrome (NCIt: C26900)
Turner syndrome (ORDO: Orphanet_881)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_UG65 ! TS1-iPS-C2
CVCL_UG66 ! TS1-iPS-C3
CVCL_UG67 ! TS1-iPS-C5
Sex of cell Female
Age at sampling 20FW
Category Induced pluripotent stem cell
Publications

PubMed=21949351; DOI=10.1093/hmg/ddr435
Li W., Wang X.-M., Fan W.-X., Zhao P., Chan Y.-C., Chen S., Zhang S.-Q., Guo X.-P., Zhang Y., Li Y.-H., Cai J.-L., Qin D.-J., Li X.-Y., Yang J.-Y., Peng T.-R., Zychlinski D., Hoffmann D., Zhang R.-S., Deng K., Ng K.-M., Menten B., Zhong M., Wu J.-Y., Li Z.-Y., Chen Y.-L., Schambach A., Tse H.-F., Pei D.-Q., Esteban M.A.
Modeling abnormal early development with induced pluripotent stem cells from aneuploid syndromes.
Hum. Mol. Genet. 21:32-45(2012)

Cross-references
Encyclopedic resources Wikidata; Q98133615
Gene expression databases GEO; GSM807102
Entry history
Entry creation13-Nov-2018
Last entry update10-Apr-2025
Version number7