ID   GENEA050
AC   CVCL_9059
SY   Genea050; SIVF050
DR   NIHhESC; NIHhESC-12-0184
DR   Wikidata; Q54835617
RX   PubMed=27217344;
RX   PubMed=27346025;
WW   Provider; Genea; -; https://web.archive.org/web/20180912205435/http://geneabiocells.com/services/shelf-products/human-embryonic-stem-cells/
CC   From: Genea Biocells, Ltd; Sydney; Australia.
CC   Registration: NIH Human Embryonic Stem Cell Registry; NIHhESC-12-0184.
CC   Registration: UK Stem Cell Bank (UKSCB); Steering comm. appl. SCSC14-54.
CC   Donor information: Embryo is sibling to that giving rise to GENEA049 (Cellosaurus=CVCL_9058).
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
ST   Source(s): PubMed=27346025
ST   Amelogenin: X,Y
ST   CSF1PO: 10,11
ST   D13S317: 11
ST   D16S539: 11
ST   D18S51: 11,15
ST   D19S433: 14,15
ST   D21S11: 28,30
ST   D2S1338: 20,25
ST   D3S1358: 15,17
ST   D5S818: 11
ST   D7S820: 8,11
ST   D8S1179: 13
ST   FGA: 21,22
ST   TH01: 6,8
ST   TPOX: 9,11
ST   vWA: 17,18
DI   NCIt; C172704; Facioscapulohumeral muscular dystrophy 1
DI   ORDO; Orphanet_269; Facioscapulohumeral dystrophy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 06-06-12; Last updated: 10-04-25; Version: 24
//
RX   PubMed=27217344; DOI=10.5966/sctm.2015-0224; PMCID=PMC4996435;
RA   Caron, Leslie
RA   Kher, Devaki
RA   Lee, Kian Leong
RA   McKernan, Robert
RA   Dumevska, Biljana
RA   Hidalgo, Alejandro
RA   Li, Jia
RA   Yang, Henry He
RA   Main, Heather
RA   Ferri, Giulia
RA   Petek, Lisa M.
RA   Poellinger, Lorenz
RA   Miller, Daniel Guthrie
RA   Gabellini, Davide
RA   Schmidt, Uli
RT   "A human pluripotent stem cell model of facioscapulohumeral muscular
RT   dystrophy-affected skeletal muscles.";
RL   Stem Cells Transl. Med. 5:1145-1161(2016).
//
RX   PubMed=27346025; DOI=10.1016/j.scr.2016.02.023;
RA   Dumevska, Biljana
RA   Chami, Omar
RA   Main, Heather
RA   McKernan, Robert
RA   Goel, Divya
RA   Schmidt, Uli
RT   "Derivation of FSHD1 affected human embryonic stem cell line
RT   Genea050.";
RL   Stem Cell Res. 16:503-506(2016).
//