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Journal of Immunology (Baltimore, Md. : 1950)|August 26, 2021
Nontypeable Haemophilus influenzae P5 Binds Human C4b-Binding Protein, Promoting Serum ResistanceOskar Thofte, Serena Bettoni, Yu-Ching Su, et al.Frontiers in Immunology|September 20, 2021
Serum Complement Activation by C4BP-IgM Fusion Protein Can Restore Susceptibility to Antibiotics in Neisseria gonorrhoeaeSerena Bettoni, Karolina Maziarz, M Rhia L Stone, et al.JCI Insight|October 30, 2019
C4BP-IgM protein as a therapeutic approach to treat Neisseria gonorrhoeae infectionsSerena Bettoni, Jutamas Shaughnessy, Karolina Maziarz, et al.Journal of Innate Immunity|January 22, 2025
Acinetobacter baumannii Clinical Isolates Resist Complement-Mediated Lysis by Inhibiting the Complement Cascade and Improperly Depositing MACMichal Magda, Wendy Boschloo, Serena Bettoni, et al.Journal of Immunology (Baltimore, Md. : 1950)|June 28, 2017
Interaction between Multimeric von Willebrand Factor and Complement: A Fresh Look to the Pathophysiology of Microvascular ThrombosisSerena Bettoni, Miriam Galbusera, Sara Gastoldi, et al.Frontiers in Immunology|June 7, 2023
C4b-binding protein inhibits particulate- and crystalline-induced NLRP3 inflammasome activationDamien Bierschenk, Nikolina Papac-Milicevic, Ian P Bresch, et al.Blood|July 20, 2014
Dynamics of complement activation in aHUS and how to monitor eculizumab therapyMarina Noris, Miriam Galbusera, Sara Gastoldi, et al.Journal of the American Society of Nephrology : JASN|October 15, 2017
Cluster Analysis Identifies Distinct Pathogenetic Patterns in C3 Glomerulopathies/Immune Complex-Mediated Membranoproliferative GNParaskevas Iatropoulos, Erica Daina, Manuela Curreri, et al.Molecular Immunology|February 20, 2016
Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcomeParaskevas Iatropoulos, Marina Noris, Caterina Mele, et al.Clinical Journal of the American Society of Nephrology : CJASN|April 10, 2015
Characterization of a New DGKE Intronic Mutation in Genetically Unsolved Cases of Familial Atypical Hemolytic Uremic SyndromeCaterina Mele, Mathieu Lemaire, Paraskevas Iatropoulos, et al.Pageof 3