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BMC Blood Disorders|June 26, 2012
Health related quality of life in Middle Eastern children with beta-thalassemiaGiovanni Caocci, Fabio Efficace, Francesca Ciotti, et al.
Blood|February 25, 2005
A proportion of patients with lymphoma may harbor mutations of the perforin geneRita Clementi, Franco Locatelli, Loïc Dupré, et al.
Bone Marrow Transplantation|August 12, 2014
BAT2 and BAT3 polymorphisms as novel genetic risk factors for rejection after HLA-related SCTIgnazio Stefano Piras, Andrea Angius, Marco Andreani, et al.
The Journal of Allergy and Clinical Immunology|May 3, 2011
Lentiviral-mediated gene therapy leads to improvement of B-cell functionality in a murine model of Wiskott-Aldrich syndromeMarita Bosticardo, Elena Draghici, Francesca Schena, et al.
Genome Biology|August 8, 2024
Transcriptional and epigenetic characterization of a new in vitro platform to model the formation of human pharyngeal endodermAndrea Cipriano, Alessio Colantoni, Alessandro Calicchio, et al.
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.
Haematologica|October 15, 2020
Engineered type 1 regulatory T cells designed for clinical use kill primary pediatric acute myeloid leukemia cellsBrandon Cieniewicz, Molly Javier Uyeda, Ping Pauline Chen, et al.
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