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Unravelling the role of retinoic acid in Tetralogy of Fallot using patient-specific iPSC-derived cardiacorganoids.
Prenatal Correction of X-Linked Hypohidrotic Ectodermal Dysplasia
„graspPURA“ | „Center for cell and gene therapy in epidermolysis bullosa“
"Molecular dissection of the neuronal ceroid lipofuscinosis causing CLN3 protein"
"Validity of diagnostic testing in Primary Ciliary Dyskinesia"
"Translational analysis of epilepsy in Phelan-McDermid syndrome and other Shankopathies"
"Investigation of the Zellweger Syndrome Specture disorders at molecular level"
"Towards a targeting protein replacement therapy for mitochondrial protein synthesis defects"