Generation of homozygous and heterozygous REEP1 knockout induced pluripotent stem cell lines by CRISPR/Cas9 gene editing
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Funder
BMBF Bonn
Publisher
Elsevier BV
Reference3 articles.
1. Beetz, Christian; Schüle, Rebecca; Deconinck, Tine; Tran-Viet, Khanh-Nhat; Zhu, Hui; Kremer, Berry P. H. et al. (2008): REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31. In: Brain: a journal of neurology 131 (Pt 4), S. 1078–1086. DOI: 10.1093/brain/awn026.
2. Hauser, Stefan; Schuster, Stefanie; Heuten, Elena; Höflinger, Philip; Admard, Jakob; Schelling, Yvonne et al. (2020): Comparative Transcriptional Profiling of Motor Neuron Disorder-Associated Genes in Various Human Cell Culture Models. In: Frontiers in cell and developmental biology 8, S. 544043. DOI: 10.3389/fcell.2020.544043.
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1. Generation of a human induced pluripotent stem cell line (FSMi001-A) from fibroblasts of a patient carrying heterozygous mutation in the REEP1 gene;Stem Cell Research;2024-09
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