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Cellosaurus KAUSTi001-B (CVCL_A9PU)

[Text version]
Cell line name KAUSTi001-B
Synonyms KS7-iPSC#B; KAUSTi002-A
Accession CVCL_A9PU
Resource Identification Initiative To cite this cell line use: KAUSTi001-B (RRID:CVCL_A9PU)
Comments From: King Abdullah University of Science and Technology; Thuwal; Saudi Arabia.
Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease 49,XXXXY syndrome (NCIt: C185635)
49,XXXXY syndrome (ORDO: Orphanet_96264)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_V753 (GM00157)
Sex of cell Male
Age at sampling 28Y
Category Induced pluripotent stem cell
Publications

PubMed=33254093; DOI=10.1016/j.scr.2020.102098
Alowaysi M., Fiacco E., Astro V., Adamo A.
Generation of two iPSC lines (KAUSTi001-A, KAUSTi002-A) from a rare high-grade Klinefelter syndrome patient (49-XXXXY) carrying a balanced translocation t(4,11) (q35,q23).
Stem Cell Res. 49:102098-102098(2020)

Cross-references
Cell line databases/resources hPSCreg; KAUSTi001-B
Biological sample resources BioSamples; SAMEA7405466
Encyclopedic resources Wikidata; Q102114352
Entry history
Entry creation29-Oct-2020
Last entry update29-Jun-2023
Version number5