ID   VUB05_HD
AC   CVCL_9842
SY   VUB-05-HD; VUBe005-A
DR   hPSCreg; VUBe005-A
DR   SKIP; SKIP001828
DR   Wikidata; Q54993389
RX   PubMed=16284066;
CC   From: Vrije Universiteit Brussel; Brussels; Belgium.
CC   Registration: UK Stem Cell Bank (UKSCB); Steering comm. appl. SCSC06-24.
CC   Sequence variation: Mutation; HGNC; HGNC:4851; HTT; Repeat_expansion; p.Gln18[44] (c.52CAG(44)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Unspecified (PubMed=16284066).
CC   Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
CC   Cell type: Embryonic stem cell; CL=CL_0002322.
DI   NCIt; C82342; Huntington's disease
DI   ORDO; Orphanet_399; Huntington disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   Blastocyst stage
CA   Embryonic stem cell
DT   Created: 06-06-12; Last updated: 19-12-24; Version: 20
//
RX   PubMed=16284066; DOI=10.1093/humrep/dei345;
RA   Mateizel, Ileana
RA   De Temmerman, Nele A.
RA   Ullmann, Urielle
RA   Cauffman, Greet
RA   Sermon, Karen
RA   van de Velde, Hilde
RA   De Rycke, Martine
RA   Degreef, Ellen
RA   Devroey, Paul
RA   Liebaers, Inge
RA   Van Steirteghem, Andre
RT   "Derivation of human embryonic stem cell lines from embryos obtained
RT   after IVF and after PGD for monogenic disorders.";
RL   Hum. Reprod. 21:503-511(2006).
//