Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Rebecca, Subang"'
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Anti-phospholipid syndrome (APS) and systemic lupus erythematosus (SLE) are autoimmune diseases characterized by autoantibody production and autoantibody-related pathology. Anti-phospholipid antibodies (aPL) are found in all patients with APS and in
Externí odkaz:
https://doaj.org/article/5381d69e579a403e9cd6c76056f6ccf2
Autor:
Erwan Pernet, Maziar Divangahi, Romain Cayrol, David Salem, Jerrold S. Levine, Christian A. Pineau, Joyce Rauch, Rebecca Subang
Publikováno v:
Immunology & Cell Biology. 97:799-814
Systemic lupus erythematosus (SLE) is characterized by the development of autoantibodies against diverse self-antigens with damage to multiple organs. Immunization with the SLE autoantigen β2 -glycoprotein I (β2 GPI) and lipopolysaccharide (LPS), a
Publikováno v:
Frontiers in Immunology, Vol 9 (2018)
Frontiers in Immunology
Frontiers in Immunology
Anti-phospholipid syndrome (APS) and systemic lupus erythematosus (SLE) are autoimmune diseases characterized by autoantibody production and autoantibody-related pathology. Anti-phospholipid antibodies (aPL) are found in all patients with APS and in
Autor:
David, Salem, Rebecca, Subang, Erwan, Pernet, Maziar, Divangahi, Christian, Pineau, Romain, Cayrol, Jerrold S, Levine, Joyce, Rauch
Publikováno v:
Immunology and cell biologyReferences. 97(9)
Systemic lupus erythematosus (SLE) is characterized by the development of autoantibodies against diverse self-antigens with damage to multiple organs. Immunization with the SLE autoantigen β
Publikováno v:
Cell Mol Immunol
Systemic lupus erythematosus is a prototypic model for B-cell epitope spread in autoimmunity. Autoantibodies to numerous molecularly distinct self-antigens emerge in a sequential manner over several years, leading to disease manifestations. Among the
Autor:
Yahye Merhi, S T Qureshi, M-A Gillis, R Fuentes, Robert Roubey, N Farhat, P Laplante, Rebecca Subang, Nigel Mackman, Jerrold S. Levine, Deeb N. Salem, Eric Thorin, Joyce Rauch, C A Fletcher, A Hachem
Publikováno v:
Lupus. 25:162-176
Patients with antiphospholipid syndrome (APS) produce antiphospholipid antibodies (aPL) and develop vascular thrombosis that may occur in large or small vessels in the arterial or venous beds. On the other hand, many individuals produce aPL and yet n
Publikováno v:
Journal of Biological Chemistry. 286:42494-42503
β(2)-Glycoprotein I (β(2)GPI) is an abundant plasma protein that binds to the surface of cells and particles expressing negatively charged lipids, but its physiological role remains unknown. Antibodies to β(2)GPI are found in patients with anti-ph
Autor:
Tanya Tolomeo, Angela Rico De Souza, Evan Roter, Mélanie Dieudé, Pascal Amireault, Rebecca Subang, Jerrold S. Levine, Joyce Rauch
Publikováno v:
Autoimmunity. 42:292-295
Anti-phospholipid syndrome (APS) is an autoimmune disorder characterized by the presence of autoantibody (AAb) to phospholipid (PL)-binding proteins, such as beta2-glycoprotein I (beta2GPI), and clinical manifestations including thrombosis and/or rec
Autor:
Joyce Rauch, Jerrold S. Levine, Yuka Okazaki, David Salem, P Laplante, Masataka Kuwana, Rebecca Subang
Publikováno v:
The Journal of biological chemistry. 290(9)
Systemic lupus erythematosus (SLE) is a prototypic model for B cell epitope spread in autoimmunity. Autoantibodies to numerous and molecularly distinct self-antigens emerge in a sequential manner over several years, leading to disease manifestations.
Autor:
Sylvie Fournier, Joyce Rauch, Joan E. Wither, Ginette Lajoie, Jerrold S. Levine, Samih H. Nasr, Rebecca Subang
Publikováno v:
The Journal of Immunology. 177:6504-6516
The initial events predisposing to loss of tolerance in patients with systemic lupus erythematosus (SLE) are largely unknown, as are the events that precipitate the transition from preclinical to overt disease. We hypothesized that induction of murin