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Cellosaurus LUMCi018-A (CVCL_ZA22)

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Cell line name LUMCi018-A
Synonyms LUMC0112iALK; LUMC0112iALK08
Accession CVCL_ZA22
Resource Identification Initiative To cite this cell line use: LUMCi018-A (RRID:CVCL_ZA22)
Comments From: Leiden University Medical Center; Leiden; Netherlands.
Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
Disease Hereditary hemorrhagic telangiectasia (NCIt: C35064)
Hereditary hemorrhagic telangiectasia (ORDO: Orphanet_774)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_F1J6 (LUMCi018-A-1)CVCL_F1J7 (LUMCi018-A-2)
Sex of cell Male
Age at sampling 55Y
Category Induced pluripotent stem cell
Publications

PubMed=40876070; DOI=10.1016/j.scr.2025.103812
Kendy Eduardo Urdaneta, Francijna E. van den Hil, Marga J. Bouma, Herak Manjikian, Christine Lindsay Mummery, Christian M.A.H. Freund, Valeria V. Orlova, Sebastiaan Johannes van Kampen;
Generation of patient-derived and gene-corrected hiPSC lines from hereditary hemorrhagic telangiectasia type 2 patients with ACVRL1 c.1042delG mutation.
Stem Cell Res. 88:103812-103812(2025)

Cross-references
Cell line databases/resources hPSCreg; LUMCi018-A
Biological sample resources BioSamples; SAMEA118679128
Encyclopedic resources Wikidata; Q98127057
Entry history
Entry creation02-Jul-2020
Last entry update27-Nov-2025
Version number4