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2. Hyperfunctional complement C3 promotes C5-dependent atypical hemolytic uremic syndrome in mice

3. Selectivity of C3-opsonin targeted complement inhibitors: A distinct advantage in the protection of erythrocytes from paroxysmal nocturnal hemoglobinuria patients

7. Factor H autoantibodies in membranoproliferative glomerulonephritis

9. Homodimeric Minimal Factor H: In Vivo Tracking and Extended Dosing Studies in Factor H Deficient Mice

10. C3 Glomerulopathy and Related Disorders in Children

13. Murine Factor H Co-Produced in Yeast With Protein Disulfide Isomerase Ameliorated C3 Dysregulation in Factor H-Deficient Mice

15. Factor I Autoantibodies in Patients with Atypical Hemolytic Uremic Syndrome

16. Factor H autoantibodies are associated with MPGN

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