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The Journal of Clinical Investigation|June 3, 2006
Defective regulatory and effector T cell functions in patients with FOXP3 mutationsRosa Bacchetta, Laura Passerini, Eleonora Gambineri, et al.
Clinical Immunology (Orlando, Fla.)|February 5, 2024
IL-10-producing regulatory cells impact on celiac disease evolutionLaura Passerini, Giada Amodio, Virginia Bassi, et al.
Frontiers in Immunology|March 2, 2018
Corrigendum: Monitoring T-Cell Responses in Translational Studies: Optimization of Dye-Based Proliferation Assay for Evaluation of Antigen-Specific ResponsesAnja Ten Brinke, Natalia Marek-Trzonkowska, Maria J Mansilla, et al.
Frontiers in Immunology|January 10, 2018
Monitoring T-Cell Responses in Translational Studies: Optimization of Dye-Based Proliferation Assay for Evaluation of Antigen-Specific ResponsesAnja Ten Brinke, Natalia Marek-Trzonkowska, Maria J Mansilla, et al.
Molecular Therapy. Methods & Clinical Development|August 18, 2025
Neonatal gene therapy effectively prevents disease manifestations in a murine model of Mucopolysaccharidosis type IGiada De Ponti, Ludovica Santi, Giorgia Dina, et al.
Biochimica Et Biophysica Acta. Molecular Cell Research|August 21, 2024
Transcriptomic analysis of BM-MSCs identified EGR1 as a transcription factor to fully exploit their therapeutic potentialLudovica Santi, Stefano Beretta, Margherita Berti, et al.
Journal of Autoimmunity|May 24, 2023
Tolerogenic IL-10-engineered dendritic cell-based therapy to restore antigen-specific tolerance in T cell mediated diseasesLaura Passeri, Grazia Andolfi, Virginia Bassi, et al.
Molecular Therapy. Methods & Clinical Development|September 16, 2024
A GLB1 transgene with enhanced therapeutic potential for the preclinical development of ex-vivo gene therapy to treat mucopolysaccharidosis type IVBStefania Crippa, Gaia Alberti, Laura Passerini, et al.
The Journal of Allergy and Clinical Immunology|December 25, 2019
Treatment with rapamycin can restore regulatory T-cell function in IPEX patientsLaura Passerini, Federica Barzaghi, Rosalia Curto, et al.
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