ID   CNS1-hiPSC1
AC   CVCL_C004
SY   CNS.1.H.iPSC.1
DR   Wikidata; Q54813886
RX   PubMed=20821352;
CC   From: Royan Institute; Theran; Iran.
CC   Population: Iranian.
CC   Sequence variation: Mutation; HGNC; 12530; UGT1A1; Simple; p.Leu413Pro; Zygosity=Unspecified (PubMed=20821352).
CC   Derived from sampling site: Skin; dermis. Cell type=Fibroblast.
DI   NCIt; C84656; Crigler-Najjar syndrome
DI   ORDO; Orphanet_205; Crigler-Najjar syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens
OI   CVCL_C006 ! CNS1-hiPSC2
OI   CVCL_C007 ! CNS1-hiPSC4
OI   CVCL_C008 ! CNS1-hiPSC5
OI   CVCL_C009 ! CNS1-hiPSC6
OI   CVCL_C010 ! CNS1-hiPSC7
OI   CVCL_C011 ! CNS1-hiPSC8
OI   CVCL_C012 ! CNS1-hiPSC9
OI   CVCL_C005 ! CNS1-hiPSC10
SX   Female
AG   19Y
CA   Induced pluripotent stem cell
DT   Created: 06-06-12; Last updated: 17-03-22; Version: 11
RX   PubMed=20821352; DOI=10.1007/s12015-010-9189-3;
RA   Ghodsizadeh A., Taei A., Totonchi M., Seifinejad A., Gourabi H.,
RA   Pournasr B., Aghdami N., Malekzadeh R., Almadani N., Salekdeh G.H.,
RA   Baharvand H.;
RT   "Generation of liver disease-specific induced pluripotent stem cells
RT   along with efficient differentiation to functional hepatocyte-like
RT   cells.";
RL   Stem Cell Rev. Rep. 6:622-632(2010).