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Cellosaurus MHHi002-A-1 (CVCL_QX53)

[Text version]

Cell line name MHHi002-A-1
Synonyms CF[1]iPS5-corr18b13w3C36
Accession CVCL_QX53
Resource Identification Initiative To cite this cell line use: MHHi002-A-1 (RRID:CVCL_QX53)
Comments From: Hannover Medical School, LEBAO (MHH); Hannover; Germany.
Characteristics: The homozygous CFTR p.Phe508del (c.1521_1523delCTT) mutation of the donor has been corrected by TALEN.
Disease Cystic fibrosis (NCIt: C2975)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_QX52 (MHHi002-A)
Sex of cell Male
Category Induced pluripotent stem cell
Publications

PubMed=28925369; DOI=10.1016/j.scr.2017.07.010
Merkert S., Bednarski C., Gohring G., Cathomen T., Martin U.
Generation of a gene-corrected isogenic control iPSC line from cystic fibrosis patient-specific iPSCs homozygous for p.Phe508del mutation mediated by TALENs and ssODN.
Stem Cell Res. 23:95-97(2017)

Cross-references
Cell line databases/resources hPSCreg; MHHi002-A-1
Other Wikidata; Q54905556
Entry history
Entry creation15-Nov-2017
Last entry updated07-Sep-2018
Version number3