ID   UMANe002-A-4
AC   CVCL_E3RS
SY   IBM13-19; UMANCe003-A-4
DR   BioSamples; SAMEA115495030
DR   hPSCreg; UMANe002-A-4
RX   PubMed=38788724;
CC   Population: Caucasian.
CC   Knockout cell: Method=CRISPR/Cas9; HGNC; HGNC:11630; HNF1B (Note=1 of 2 alleles).
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_L201 ! Man-13
SX   Male
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 19-12-24; Last updated: 19-12-24; Version: 1
//
RX   PubMed=38788724; DOI=10.1016/j.stemcr.2024.04.011; PMCID=PMC11297557;
RA   Bantounas I., Rooney K.M., Lopes F.M., Tengku F., Woods S., Zeef L.A.H.,
RA   Lin I.-H., Kuba S.Y., Bates N., Hummelgaard S., Hillman K.A.,
RA   Cereghini S., Woolf A.S., Kimber S.J.;
RT   "Human pluripotent stem cell-derived kidney organoids reveal tubular
RT   epithelial pathobiology of heterozygous HNF1B-associated dysplastic
RT   kidney malformations.";
RL   Stem Cell Reports 19:859-876(2024).
//