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Cellosaurus LCA1-hiPSC3 (CVCL_C816)

[Text version]
Cell line name LCA1-hiPSC3
Synonyms LCA.1.H.iPSC.3; LCA-hiPSC3
Accession CVCL_C816
Resource Identification Initiative To cite this cell line use: LCA1-hiPSC3 (RRID:CVCL_C816)
Comments From: Royan Institute; Theran; Iran.
Population: Iranian.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Leber congenital amaurosis (NCIt: C129075)
Leber congenital amaurosis (ORDO: Orphanet_65)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_C814 ! LCA1-hiPSC1
CVCL_C815 ! LCA1-hiPSC2
CVCL_C817 ! LCA1-hiPSC4
Sex of cell Male
Age at sampling 17Y
Category Induced pluripotent stem cell
Publications

PubMed=22145677; DOI=10.1089/scd.2011.0599
Zahabi A., Shahbazi E., Ahmadieh H., Hassani S.-N., Totonchi M., Taei A., Masoudi N.S., Ebrahimi M., Aghdami N., Seifinejad A., Mehrnejad F., Daftarian N., Salekdeh G.H., Baharvand H.
A new efficient protocol for directed differentiation of retinal pigmented epithelial cells from normal and retinal disease induced pluripotent stem cells.
Stem Cells Dev. 21:2262-2272(2012)

Cross-references
Cell line collections (Providers) RSCB; RSCB0098
Encyclopedic resources Wikidata; Q54902185
Entry history
Entry creation22-Oct-2012
Last entry update29-Jun-2023
Version number11