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Nature Communications|March 15, 2022
A systematic review and meta-analysis of gene therapy with hematopoietic stem and progenitor cells for monogenic disordersFrancesca Tucci, Stefania Galimberti, Luigi Naldini, et al.Human Gene Therapy|March 21, 2006
Efficacy of gene therapy for Wiskott-Aldrich syndrome using a WAS promoter/cDNA-containing lentiviral vector and nonlethal irradiationLoïc Dupré, Francesco Marangoni, Samantha Scaramuzza, et al.Nature Reviews. Genetics|March 30, 2011
Ex vivo gene transfer and correction for cell-based therapiesLuigi NaldiniEMBO Molecular Medicine|January 24, 2019
Genetic engineering of hematopoiesis: current stage of clinical translation and future perspectivesLuigi NaldiniCurrent Opinion in Molecular Therapeutics|November 19, 2002
Advances in gene therapy for ADA-deficient SCIDAlessandro AiutiBest Practice & Research. Clinical Haematology|October 23, 2004
Gene therapy for adenosine-deaminase-deficient severe combined immunodeficiencyAlessandro AiutiStem Cell Reports|March 24, 2017
Efficient Ex Vivo Engineering and Expansion of Highly Purified Human Hematopoietic Stem and Progenitor Cell Populations for Gene TherapyErika Zonari, Giacomo Desantis, Carolina Petrillo, et al.Cell Stem Cell|May 5, 2023
Genetic engineering meets hematopoietic stem cell biology for next-generation gene therapySamuele Ferrari, Erika Valeri, Anastasia Conti, et al.Cell Stem Cell|November 10, 2019
In Vivo Selection for Gene-Corrected HSPCs Advances Gene Therapy for a Rare Stem Cell DiseaseBernhard Gentner, Luigi NaldiniPageof 43