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Cellosaurus UHOMe001-A (CVCL_C391)

[Text version]

Cell line name UHOMe001-A
Synonyms HD90; HD90/FE07-142-L1; HD90/D18/FE07-142-L1; HD90/D18E7; D18
Accession CVCL_C391
Resource Identification Initiative To cite this cell line use: UHOMe001-A (RRID:CVCL_C391)
Comments From: University Hospital of Montpellier; Montpellier; France.
Registration: French Agence de la Biomedecine; FE07-142-L1.
Disease Von Hippel-Lindau syndrome (NCIt: C3105)
Von Hippel-Lindau disease (ORDO: Orphanet_892)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling Blastocyst stage
Category Embryonic stem cell
Web pages http://www.agence-biomedecine.fr/IMG/pdf/chu_montpellier_hd90.pdf

PubMed=19128516; DOI=10.1186/1471-2164-10-10
Assou S., Cerecedo D., Tondeur S., Pantesco V., Hovatta O., Klein B., Hamamah S., De Vos J.
A gene expression signature shared by human mature oocytes and embryonic stem cells.
BMC Genomics 10:10-10(2009)

Pellestor F., Monzo C., Nadal L., De Vos J., Hamamah S.
Acquisition of a trisomy 20 in the human embryonic stem cell line HD90.
Reprod. BioMed. Online 20 Suppl. 1:S41-S41(2011)

Cell line databases/resources hPSCreg; UHOMe001-A
SKIP; SKIP002299
Other Wikidata; Q54990169
Entry history
Entry creation22-Oct-2012
Last entry updated12-Mar-2020
Version number10