ID   SZ-FX1
AC   CVCL_Y330
SY   SZ-FX1 PGD; FX#1
DR   NIHhESC; NIHhESC-20-0440
DR   Wikidata; Q54971304
RX   PubMed=21585244;
RX   PubMed=27690107;
WW   https://www.szmc.org.il/UploadFiles/12_2016/HESC.pdf
CC   From: Shaare Zedek Medical Center, The Hebrew University; Jerusalem; Israel.
CC   Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-20-0440.
CC   Sequence variation: Mutation; HGNC; HGNC:3775; FMR1; Repeat_expansion; CGG[75]; ClinVar=VCV000009972; Zygosity=Unspecified (PubMed=21585244).
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)
SX   Female
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 07-11-14; Last updated: 19-12-24; Version: 12
//
RX   PubMed=21585244; DOI=10.1089/scd.2011.0102; PMCID=PMC3272241;
RA   Ben-Yosef D., Amit A., Malcov M., Frumkin T., Ben-Yehudah A.,
RA   Eldar I., Mey-Raz N., Azem F., Altarescu G., Renbaum P., Beeri R.,
RA   Varshaver I., Eldar-Geva T., Epsztejn-Litman S., Levy-Lahad E.,
RA   Eiges R.;
RT   "Female sex bias in human embryonic stem cell lines.";
RL   Stem Cells Dev. 21:363-372(2012).
//
RX   PubMed=27690107; DOI=10.3390/genes7100077; PMCID=PMC5083916;
RA   Mor-Shaked H., Eiges R.;
RT   "Modeling fragile X syndrome using human pluripotent stem cells.";
RL   Genes (Basel) 7:77.1-77.19(2016).
//