ID   CNS2-hiPSC6
AC   CVCL_C018
SY   CNS.2.H.iPSC.6
DR   Wikidata; Q54813911
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_C013 ! CNS2-hiPSC1
OI   CVCL_C014 ! CNS2-hiPSC2
OI   CVCL_C015 ! CNS2-hiPSC3
OI   CVCL_C016 ! CNS2-hiPSC4
OI   CVCL_C017 ! CNS2-hiPSC5
OI   CVCL_C019 ! CNS2-hiPSC7
OI   CVCL_C020 ! CNS2-hiPSC8
SX   Male
AG   21Y
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).