ID   CNS2-hiPSC1
AC   CVCL_C013
SY   CNS.2.H.iPSC.1
DR   RSCB; RSCB0140
DR   Wikidata; Q54813906
RX   PubMed=20821352;
CC   From: Royan Institute; Theran; Iran.
CC   Population: Iranian.
CC   Sequence variation: Mutation; HGNC; HGNC:12530; UGT1A1; Simple; p.Leu413Pro; Zygosity=Unspecified (PubMed=20821352).
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C84656; Crigler-Najjar syndrome
DI   ORDO; Orphanet_205; Crigler-Najjar syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_C014 ! CNS2-hiPSC2
OI   CVCL_C015 ! CNS2-hiPSC3
OI   CVCL_C016 ! CNS2-hiPSC4
OI   CVCL_C017 ! CNS2-hiPSC5
OI   CVCL_C018 ! CNS2-hiPSC6
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: 19-12-24; Version: 14
//
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).
//