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Cellosaurus PH1-iPSC#2 (CVCL_A4WD)

[Text version]
Cell line name PH1-iPSC#2
Accession CVCL_A4WD
Resource Identification Initiative To cite this cell line use: PH1-iPSC#2 (RRID:CVCL_A4WD)
Comments From: University of Bordeaux; Bordeaux; France.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
Disease Primary hyperoxaluria type I (NCIt: C123212)
Primary hyperoxaluria type 1 (ORDO: Orphanet_93598)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_A4WG (PH1-iPSC#2-TTRp-AGXT)CVCL_A4WH (PH1-iPSC#2-TTRp-eGFP)
Originate from same individual CVCL_A4WC ! PH1-iPSC#1
Sex of cell Male
Age at sampling Age unspecified
Category Induced pluripotent stem cell
Publications

PubMed=31151050; DOI=10.1016/j.scr.2019.101467
Esteve J., Blouin J.-M., Lalanne M., Azzi-Martin L., Dubus P., Bidet A., Harambat J., Llanas B., Moranvillier I., Bedel A., Moreau-Gaudry F., Richard E.
Generation of induced pluripotent stem cells-derived hepatocyte-like cells for ex vivo gene therapy of primary hyperoxaluria type 1.
Stem Cell Res. 38:101467-101467(2019)

Cross-references
Encyclopedic resources Wikidata; Q107116660
Entry history
Entry creation20-May-2021
Last entry update19-Dec-2024
Version number6