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Journal of Immunology (Baltimore, Md. : 1950)|November 4, 2006
Defective Th1 cytokine gene transcription in CD4+ and CD8+ T cells from Wiskott-Aldrich syndrome patientsSara Trifari, Giovanni Sitia, Alessandro Aiuti, et al.The Journal of Allergy and Clinical Immunology|July 11, 2017
Peanut-specific type 1 regulatory T cells induced in vitro from allergic subjects are functionally impairedLaurence Pellerin, Jennifer Anne Jenks, Sharon Chinthrajah, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|November 7, 2007
Generation of potent and stable human CD4+ T regulatory cells by activation-independent expression of FOXP3Sarah E Allan, Alicia N Alstad, Natacha Merindol, et al.Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|August 19, 2007
Frequency and targeted detection of HLA-DPB1 T cell epitope disparities relevant in unrelated hematopoietic stem cell transplantationElisabetta Zino, Luca Vago, Simona Di Terlizzi, et al.Journal of Immunology (Baltimore, Md. : 1950)|September 5, 2006
Gliadin-specific type 1 regulatory T cells from the intestinal mucosa of treated celiac patients inhibit pathogenic T cellsCarmen Gianfrani, Megan K Levings, Claudia Sartirana, et al.The Journal of Allergy and Clinical Immunology|April 30, 2018
Role of human forkhead box P3 in early thymic maturation and peripheral T-cell homeostasisFrancesca R Santoni de Sio, Laura Passerini, Silvia Restelli, et al.Haematologica|August 18, 2010
Molecular and functional characterization of allogantigen-specific anergic T cells suitable for cell therapyRosa Bacchetta, Silvia Gregori, Giorgia Serafini, et al.Experimental Hematology|April 23, 2022
Downregulation of SATB1 by miRNAs reduces megakaryocyte/erythroid progenitor expansion in preclinical models of Diamond-Blackfan anemiaMark C Wilkes, Vanessa Scanlon, Aya Shibuya, et al.Cytotherapy|August 18, 2021
Pre-clinical development and molecular characterization of an engineered type 1 regulatory T-cell product suitable for immunotherapyJeffrey Mao-Hwa Liu, Ping Chen, Molly Javier Uyeda, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|October 29, 2004
Lentiviral vector-mediated gene transfer in T cells from Wiskott-Aldrich syndrome patients leads to functional correctionLoïc Dupré, Sara Trifari, Antonia Follenzi, et al.Pageof 20