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Stem Cell Reports|November 25, 2021
Simultaneous high-efficiency base editing and reprogramming of patient fibroblastsSami Jalil, Timo Keskinen, Rocío Maldonado, et al.
Molecular Genetics and Metabolism Reports|July 5, 2022
CRISPR correction of the Finnish ornithine delta-aminotransferase mutation restores metabolic homeostasis in iPSC from patients with gyrate atrophyRocio Maldonado, Sami Jalil, Timo Keskinen, et al.
Journal of Inherited Metabolic Disease|December 2, 2025
Genetic Correction of the Most Common Mutation Causing Primary Hyperoxaluria Restores Enzyme Localization and Oxalate MetabolismTimo Keskinen, Sami Jalil, Irem Gümüşoğlu, et al.
American Journal of Human Genetics|April 5, 2024
Genetic and functional correction of argininosuccinate lyase deficiency using CRISPR adenine base editorsSami Jalil, Timo Keskinen, Juhana Juutila, et al.
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