Generation of human induced pluripotent stem cell lines from a subject with UBAP1L-associated retinal dystrophy and CRISPR/cas9-corrected isogenic iPSC lines-Reference-Cited by-同舟云学术

Generation of human induced pluripotent stem cell lines from a subject with UBAP1L-associated retinal dystrophy and CRISPR/cas9-corrected isogenic iPSC lines

Published:2024-09 Issue: Volume: Page:103558
ISSN:1873-5061
Container-title:Stem Cell Research
language:en
Short-container-title:Stem Cell Research

Author:

Amprou Andréa^ORCID,Yacoub Tasnim Ben,Letellier Camille,Dagaetano Vincenzo,Méjécase Cécile,Pormehr Leila Azizzadeh,Condroyer Christel,Slembrouck-Brec Amélie,Wohlschlegel Juliette,Goureau Olivier,Zeitz Christina,Audo Isabelle

Funder

French National Research Agency

Foundation Fighting Blindness Inc

Publisher

Elsevier BV

Reference6 articles.

1. Recurrent genetic abnormalities in human pluripotent stem cells: definition and routine detection in culture supernatant by targeted droplet digital PCR;Assou;Stem Cell Rep.,2020

2. Ben Yacoub, T., Letellier, C., Wohlschlegel, J., Condroyer, C., Slembrouck-Brec, A., Goureau, O., et al., 2023. Generation of gene corrected human isogenic iPSC lines (IDVi003-A_CR13, IDVi003-A_CR21, IDVi003-A_CR24) from an inherited retinal dystrophy patient-derived IPSC line ITM2B-5286-3 (IDVi003-A) carrying the ITM2B c.782A > C variant using CRISPR/Cas9. Stem Cell Res., 71, 103166. doi: 10.1016/j.scr.2023.103166.

3. Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration;Han;Genet. Med.,2024

4. Generation of storable retinal organoids and retinal pigmented epithelium from adherent human iPS Cells in xeno-free and feeder-free conditions;Reichman;Stem Cells,2017

5. Establishment of an induced pluripotent stem (iPS) cell line from dermal fibroblasts of an asymptomatic patient with dominant PRPF31 mutation;Terray;Stem Cell Res.,2017