Biblio
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Stem Cell Res. 2018;34:101359.
Generation of 5 induced pluripotent stem cell lines, LUMCi007-A and B and LUMCi008-A, B and C, from 2 patients with Huntington disease. Stem Cell Res. 2019;39:101498.
Generation of genetically matched hiPSC lines from two mosaic facioscapulohumeral dystrophy type 1 patients. Stem Cell Res. 2019;40:101560.
. Generation and genetic repair of 2 iPSC clones from a patient bearing a heterozygous c.1120del18 mutation in the ACVRL1 gene leading to Hereditary Hemorrhagic Telangiectasia (HHT) type 2. Stem Cell Res. 2020;46:101786.
. Generation of human induced pluripotent stem cell line LUMCi027-A and its isogenic gene-corrected line from a patient affected by arrhythmogenic cardiomyopathy and carrying the c.2013delC PKP2 mutation. Stem Cell Res. 2020;46:101835.
. Generation of two human induced pluripotent stem cell lines, LUMCi020-A and LUMCi021-A, from two patients with Catecholaminergic Polymorphic Ventricular Tachycardia carrying heterozygous mutations in the RYR2 gene. Stem Cell Res. 2020;45:101764.
. Reprogramming Urine-Derived Cells using Commercially Available Self-Replicative RNA and a Single Electroporation. Curr Protoc Stem Cell Biol. 2020;55(1):e124.
. Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids. Stem Cell Reports. 2022.
. Generation of AAVS1 and CLYBL STRAIGHT-IN v2 acceptor human iPSC lines for integrating DNA payloads. Stem Cell Res. 2022;66:102991.
. AAV-mediated gene augmentation therapy of CRB1 patient-derived retinal organoids restores the histological and transcriptional retinal phenotype. Stem Cell Reports. 2023;18(6):1388.
CRB1 is required for recycling by RAB11A+ vesicles in human retinal organoids. Stem Cell Reports. 2023.
Efficient and scalable generation of primordial germ cells in 2D culture using basement membrane extract overlay. Cell Rep Methods. 2023;3(6):100488.
Genetic repair of a human induced pluripotent cell line from patient with Dutch-type cerebral amyloid angiopathy. Stem Cell Res. 2023;71:103180.
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