Eugenio Montini
Milan, 20132, Italy
Last Updated: 09/26/2026
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Found 79 publications
Tweaking lentiviral vector design balances efficacy and safety in liver-directed gene therapy for familial hypercholesterolemia.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: October 14, 2025
Ex vivo expansion of hematopoietic stem and progenitor cells from human mobilized peripheral blood for gene therapy applications.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: October 10, 2025
Gene therapy supports long-term reconstitution of patient hematopoietic stem cells in deficiency of adenosine deaminase 2.
Journal: Molecular therapy. Methods & clinical development
Published: September 16, 2025
In-depth characterization of stem cell potency and genotoxicity for clinical-scale ex vivo CRISPR-Cas9 gene editing.
Journal: Molecular therapy. Advances
Published: August 01, 2025
APOBEC3 and the mutational signature of lentiviral vectors.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: June 29, 2025
RAAVioli: A comprehensive approach to characterizing AAV vector integrations and rearrangements.
Journal: Molecular therapy. Advances
Published: June 20, 2025
Tumor-targeted interferon-α gene therapy for glioblastoma: a phase 1 trial.
Journal: Nature medicine
Published: June 18, 2025
Nanoengineered 3D culture substrate enables superior persistence and polyclonal engraftment of genetically engineered hematopoietic stem cells.
Journal: Cell stem cell
Published: June 18, 2025
Long-Term Effects of Atidarsagene Autotemcel for Metachromatic Leukodystrophy.
Journal: The New England journal of medicine
Published: April 23, 2025
Liver-directed lentiviral gene therapy confers durable hepatic and systemic amelioration of methylmalonic acidemia in mice.
Journal: Journal of hepatology
Published: March 28, 2025
Response to: Safety and efficacy considerations of HSC-based gene therapy for RAG1-deficient SCID.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: March 12, 2025
Donor-derived CARCIK-CD19 cells engineered with Sleeping Beauty transposon in acute lymphoblastic leukemia relapsed after allogeneic transplantation.
Journal: Blood cancer journal
Published: January 08, 2025
Last Updated: 09/26/2026