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The Journal of Experimental Medicine|March 25, 2009
The Wiskott-Aldrich syndrome protein is required for iNKT cell maturation and functionMichela Locci, Elena Draghici, Francesco Marangoni, et al.
The Journal of Clinical Investigation|May 4, 2007
A hypomorphic R229Q Rag2 mouse mutant recapitulates human Omenn syndromeVeronica Marrella, Pietro Luigi Poliani, Anna Casati, et al.
Journal of Autoimmunity|December 28, 2013
Wiskott-Aldrich Syndrome protein deficiency perturbs the homeostasis of B-cell compartment in humansMaria Carmina Castiello, Marita Bosticardo, Francesca Pala, et al.
Frontiers in Immunology|May 18, 2017
In Vivo Chronic Stimulation Unveils Autoreactive Potential of Wiskott-Aldrich Syndrome Protein-Deficient B CellsMaria Carmina Castiello, Francesca Pala, Lucia Sereni, et al.
Bone Reports|January 16, 2020
Generation of an immunodeficient mouse model of tcirg1-deficient autosomal recessive osteopetrosisEleonora Palagano, Sharon Muggeo, Laura Crisafulli, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 5, 2009
Evidence for long-term efficacy and safety of gene therapy for Wiskott-Aldrich syndrome in preclinical modelsFrancesco Marangoni, Marita Bosticardo, Sabine Charrier, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 2005
Rescue of ATPa3-deficient murine malignant osteopetrosis by hematopoietic stem cell transplantation in uteroAnnalisa Frattini, Harry C Blair, Maria Grazia Sacco, et al.
Stem Cell Reports|September 8, 2015
Targeted Gene Correction in Osteopetrotic-Induced Pluripotent Stem Cells for the Generation of Functional OsteoclastsTui Neri, Sharon Muggeo, Marianna Paulis, et al.
Frontiers in Immunology|June 18, 2021
Premature Senescence and Increased Oxidative Stress in the Thymus of Down Syndrome PatientsGenni Enza Marcovecchio, Francesca Ferrua, Elena Fontana, et al.
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