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Cellosaurus IMGTi001-A (CVCL_VQ13)

[Text version]

Cell line name IMGTi001-A
Synonyms iPSC-r(22)-1; iTAF5-29
Accession CVCL_VQ13
Resource Identification Initiative To cite this cell line use: IMGTi001-A (RRID:CVCL_VQ13)
Comments From: Research Institute of Medical Genetics; Tomsk; Russia.
Population: Caucasian.
Karyotypic information: r(22),del22q13.32-q13.33,dup22q13.32,del3q13.31 (PubMed=30144655).
Derived from sampling site: Skin.
Disease Phelan-McDermid syndrome (NCIt: C157124)
Ring chromosome 22 syndrome (NCIt: C179702)
Monosomy 22q13.3 (ORDO: Orphanet_48652)
Ring chromosome 22 syndrome (ORDO: Orphanet_1446)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_A9Q1 (TAF5)
Sex of cell Female
Age at sampling 3Y
Category Induced pluripotent stem cell
Publications

PubMed=30144655; DOI=10.1016/j.scr.2018.08.012
Nikitina T.V., Menzorov A.G., Kashevarova A.A., Gridina M.M., Khabarova A.A., Yakovleva Y.S., Lopatkina M.E., Kizilova E.A., Vasilyev S.A., Serov O.L., Lebedev I.N.
Generation of two iPSC lines (IMGTi001-A and IMGTi001-B) from human skin fibroblasts with ring chromosome 22.
Stem Cell Res. 31:244-248(2018)

DOI=10.1134/S1022795419100090
Nikitina T.V., Kashevarova A.A., Lebedev I.N.
Chromosomal instability and karyotype correction in human induced pluripotent stem cells.
Russ. J. Genet. 55:1183-1195(2019)

PubMed=33619287; DOI=10.1038/s41598-021-83399-3
Nikitina T.V., Kashevarova A.A., Gridina M.M., Lopatkina M.E., Khabarova A.A., Yakovleva Y.S., Menzorov A.G., Minina Y.A., Pristyazhnyuk I.E., Vasilyev S.A., Fedotov D.A., Serov O.L., Lebedev I.N.
Complex biology of constitutional ring chromosomes structure and (in)stability revealed by somatic cell reprogramming.
Sci. Rep. 11:4325-4325(2021)

Cross-references
Cell line databases/resources hPSCreg; IMGTi001-A
Biological sample resources BioSamples; SAMEA4862236
Other Wikidata; Q94316254
Entry history
Entry creation07-Sep-2018
Last entry update23-Sep-2021
Version number7