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Current Opinion in Allergy and Clinical Immunology|September 26, 2009
New insights into the pathogenesis of adenosine deaminase-severe combined immunodeficiency and progress in gene therapyAisha V Sauer, Alessandro AiutiCell Biology and Toxicology|February 11, 2015
Three common pathways of nephrotoxicity induced by halogenated alkenesPatrizia Cristofori, Aisha V Sauer, Andrea TrevisanCurrent Opinion in Allergy and Clinical Immunology|September 11, 2014
Progress in gene therapy for primary immunodeficiencies using lentiviral vectorsAisha V Sauer, Biagio Di Lorenzo, Nicola Carriglio, et al.The Journal of Clinical Investigation|May 25, 2012
Defective B cell tolerance in adenosine deaminase deficiency is corrected by gene therapyAisha V Sauer, Henner Morbach, Immacolata Brigida, et al.International Journal of Molecular Sciences|August 26, 2022
Monitoring Anti-PEG Antibodies Level upon Repeated Lipid Nanoparticle-Based COVID-19 Vaccine AdministrationGiuditta Guerrini, Sabrina Gioria, Aisha V Sauer, et al.Journal of Molecular Medicine (Berlin, Germany)|August 27, 2017
A map of human circular RNAs in clinically relevant tissuesPhilipp G Maass, Petar Glažar, Sebastian Memczak, et al.Breast Cancer Research and Treatment|December 11, 2008
Identification and functional analysis of novel BRCA1 transcripts, including mouse Brca1-Iris and human pseudo-BRCA1Christopher A Pettigrew, Juliet D French, Jodi M Saunus, et al.Human Gene Therapy. Clinical Development|March 21, 2017
Good Laboratory Practice Preclinical Safety Studies for GSK2696273 (MLV Vector-Based Ex Vivo Gene Therapy for Adenosine Deaminase Deficiency Severe Combined Immunodeficiency) in NSG MiceNicola Carriglio, Jan Klapwijk, Raisa Jofra Hernandez, et al.Blood|December 21, 2011
Alterations in the adenosine metabolism and CD39/CD73 adenosinergic machinery cause loss of Treg cell function and autoimmunity in ADA-deficient SCIDAisha V Sauer, Immacolata Brigida, Nicola Carriglio, et al.Blood|July 28, 2009
ADA-deficient SCID is associated with a specific microenvironment and bone phenotype characterized by RANKL/OPG imbalance and osteoblast insufficiencyAisha V Sauer, Emanuela Mrak, Raisa Jofra Hernandez, et al.Pageof 2