ID   CNS1-hiPSC9
AC   CVCL_C012
SY   CNS.1.H.iPSC.9
DR   Wikidata; Q54813904
RX   PubMed=20821352;
CC   From: Royan Institute; Theran; Iran.
CC   Sequence variation: UGT1A1 p.Leu413Pro (PubMed=20821352).
DI   NCIt; C84656; Crigler-Najjar syndrome
DI   ORDO; Orphanet_205; Crigler-Najjar syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens
OI   CVCL_C004 ! CNS1-hiPSC1
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_C005 ! CNS1-hiPSC10
SX   Female
AG   19Y
CA   Induced pluripotent stem cell
DT   Created: 06-06-12; Last updated: 12-03-20; Version: 8
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. 6:622-632(2010).