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Cellosaurus CBRCULi012-A (CVCL_C9J0)

[Text version]
Cell line name CBRCULi012-A
Synonyms GM04601-21; GM04601 clone 21
Accession CVCL_C9J0
Resource Identification Initiative To cite this cell line use: CBRCULi012-A (RRID:CVCL_C9J0)
Comments From: CERVO Brain Research Centre, Universite Laval; Quebec; Canada.
Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Dystrophia myotonica 1 (NCIt: C84679)
Steinert myotonic dystrophy (ORDO: Orphanet_273)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_Y793 (GM04601)
Sex of cell Female
Age at sampling 4Y
Category Induced pluripotent stem cell
Publications

PubMed=37871474; DOI=10.1016/j.scr.2023.103234
De Serres-Berard T., Jauvin D., Puymirat J., Chahine M.
Generation of induced pluripotent stem cell lines from pediatric patients with congenital myotonic dystrophy (CBRCULi012-A and CBRCULi013-A) and age-matched controls (CBRCULi010-A and CBRCULi011-A).
Stem Cell Res. 72:103234-103234(2023)

Cross-references
Cell line databases/resources hPSCreg; CBRCULi012-A
Biological sample resources BioSamples; SAMEA114243996
Encyclopedic resources Wikidata; Q123030870
Entry history
Entry creation05-Oct-2023
Last entry update30-Jan-2024
Version number2