Home  |  Contact

Cellosaurus DMBi001-A-1 (CVCL_A7LC)

[Text version]

Cell line name DMBi001-A-1
Accession CVCL_A7LC
Resource Identification Initiative To cite this cell line use: DMBi001-A-1 (RRID:CVCL_A7LC)
Comments From: Department of Medical Biotechnology, Jagiellonian University; Krakow; Poland.
Population: Caucasian.
Knockout cell: Method=CRISPR/Cas9; HGNC; 6482; LAMA2.
Derived from sampling site: Peripheral blood.
Disease Merosin-deficient congenital muscular dystrophy type 1A (NCIt: C118783)
Laminin subunit alpha 2-related congenital muscular dystrophy (ORDO: Orphanet_258)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_ZC40 (DMBi001-A)
Sex of cell Male
Age at sampling 58Y
Category Induced pluripotent stem cell
Publications

PubMed=34509921; DOI=10.1016/j.scr.2021.102529
Jelinkova S., Martyniak A., Dulak J., Stepniewski J.
Derivation of human pluripotent stem cell line via CRISPR/Cas9 mediated deletion of exon 3 LAMA2 gene (DMBi001-A-1).
Stem Cell Res. 56:102529-102529(2021)

Cross-references
Cell line databases/resources hPSCreg; DMBi001-A-1
Biological sample resources BioSamples; SAMEA8770928
Encyclopedic resources Wikidata; Q107114814
Entry history
Entry creation20-May-2021
Last entry update23-Sep-2021
Version number2