ID   Lis13_Alport2
AC   CVCL_B936
SY   Lis13_Alport_2
DR   Wikidata; Q54902600
RX   PubMed=20186514;
RX   PubMed=21585244;
CC   From: Tel-Aviv Sourasky Medical Center; Tel-Aviv; Israel.
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
DI   NCIt; C34842; Alport syndrome
DI   ORDO; Orphanet_63; Alport syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 06-06-12; Last updated: 10-09-24; Version: 14
//
RX   PubMed=20186514; DOI=10.1007/s11626-010-9275-5;
RA   Frumkin, Tsvia
RA   Malcov, Mira
RA   Telias, Michael
RA   Gold, Veronica
RA   Schwartz, Tamar
RA   Azem, Foad
RA   Amit, Ami
RA   Yaron, Yuval
RA   Ben-Yosef, Dalit
RT   "Human embryonic stem cells carrying mutations for severe genetic
RT   disorders.";
RL   In Vitro Cell. Dev. Biol. Anim. 46:327-336(2010).
//
RX   PubMed=21585244; DOI=10.1089/scd.2011.0102; PMCID=PMC3272241;
RA   Ben-Yosef, Dalit
RA   Amit, Ami
RA   Malcov, Mira
RA   Frumkin, Tsvia
RA   Ben-Yehudah, Ahmi
RA   Eldar, Ido
RA   Mey-Raz, Nava
RA   Azem, Foad
RA   Altarescu, Gheona
RA   Renbaum, Paul
RA   Beeri, Rachel
RA   Varshaver, Irit
RA   Eldar-Geva, Talia
RA   Epsztejn-Litman, Silvina
RA   Levy-Lahad, Ephrat
RA   Eiges, Rachel
RT   "Female sex bias in human embryonic stem cell lines.";
RL   Stem Cells Dev. 21:363-372(2012).
//