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Premature aging in neonatal mitohochondrial disease: molecular mechanisms and treatments.Jane and Aatos Erkko FoundationJukka Kallijärvi2024Bone, gut, and gonad connections in APS-1 - A prospective cohort studyResearch Council of FinlandHelsingin seudun yliopistollisen keskussairaalan erityisvastuualue2023Modeling of human GLE1 mutations in mice to understand RNA metabolism in vivoResearch Council of FinlandHelsingin yliopisto2022Gene correction and disease modelling of the Finnish heritage diseases Familial Hypercholesterolemia and Argininosuccinate Lyase Deficiency in patient-derived pluripotent stem cells.The Paulo FoundationSami Jalil2022
Premature aging in neonatal mitohochondrial disease: molecular mechanisms and treatments.
2024
Bone, gut, and gonad connections in APS-1 - A prospective cohort study
2023
Modeling of human GLE1 mutations in mice to understand RNA metabolism in vivo
2022
Gene correction and disease modelling of the Finnish heritage diseases Familial Hypercholesterolemia and Argininosuccinate Lyase Deficiency in patient-derived pluripotent stem cells.
2022