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Autor:
Rudolph C. Kuppers, Douglas A. Jabs, C. Lynne Burek, Robert A. Prendergast, Ali M. Saboori, Cheryl Enger, Bella Lee
Publikováno v:
Cellular Immunology. 154:66-76
MRL/Mp-Ipr/Ipr (MRL/Ipr) mice spontaneously develop a systemic autoimmune disease, characterized by vasculitis, lymphadenopathy, glomerulortephritis, and autoantibody formation, with target organ inflammatory lesions composed largely of CD4+ (helper)