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Donor species complement after liver xenotransplantation. The mechanism of protection from hyperacute rejection.
Painting factor H onto mesenchymal stem cells protects the cells from complement- and neutrophil-mediated damage.
Prospects of clinical xenotransplantation.
Interleukin-2 and interleukin-12 mediate distinct effector mechanisms of liver allograft rejection.
Complement mediated hepatocytes injury in a model of autoantibody induced hepatitis.
Presence of retinal pericyte-reactive autoantibodies in diabetic retinopathy patients.
Local Inhibition of Complement Improves Mesenchymal Stem Cell Viability and Function After Administration.