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Cellosaurus iPS ARPKD 4 (CVCL_V452)

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Cell line name iPS ARPKD 4
Accession CVCL_V452
Resource Identification Initiative To cite this cell line use: iPS ARPKD 4 (RRID:CVCL_V452)
Comments Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Autosomal recessive polycystic kidney disease (NCIt: C84579)
Autosomal recessive polycystic kidney disease (ORDO: Orphanet_731)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_V446 (GM10287)
Sex of cell Male
Age at sampling 36FW
Category Induced pluripotent stem cell
Publications

PubMed=24009235; DOI=10.1681/ASN.2012111089; PMCID=PMC3785271
Benjamin S. Freedman, Albert Q. Lam, Jamie L. Sundsbak, Rossella Iatrino, Xue-Feng Su, Sarah J. Koon, Mao-Qing Wu, Laurence Daheron, Peter C. Harris, Jing Zhou, Joseph Vincent Bonventre;
Reduced ciliary polycystin-2 in induced pluripotent stem cells from polycystic kidney disease patients with PKD1 mutations.
J. Am. Soc. Nephrol. 24:1571-1586(2013)

Cross-references
Encyclopedic resources Wikidata; Q54898075
Entry history
Entry creation16-Apr-2014
Last entry update29-Jun-2023
Version number9