Exploring base editing for the correction of nonsense mutations in hemophilia B

Caratterizzazione dei determinanti molecolari del processo di soppressione di mutazioni nonsenso mediato da ribosome readthrough

Do residual FVIII levels associated with F8 nonsense mutations reduce the inhibitor risk in hemophilia A patients?

Factor IX variants with superior pharmacokinetics as next-generation therapeutics for Haemophilia B

Hemophilia A patients with nonsense mutations: residual factor VIII expression levels and development of inhibitory antibodies

Improved intracellular processing of protein variants as a personalized therapeutic approach for Haemophilia

Editorial Board Member della rivista International Journal of Biochemistry & Cell Biology

Editorial Board Member della rivista DNA and Cell Biology

Associate Editor per la rivista Frontiers in Pediatrics - sezione Genetic Disorders

Academic Editor per la rivista PLoS One

Associate Editor per la rivista Frontiers in Genetics - sezione Genetic Disorders

Review Editor per la rivista Frontiers in Molecular Biosciences - sezione Molecular Diagnostics and Therapeutics

Rview Editor per la rivista Frontiers in Pediatrics - sezione Genetic Disorders

Review Editor per la rivista Frontiers in Genetics - sezione Genetic Disorders

Review Editor per la rivista Frontiers in Cell and Developmental Biology