Pages that link to "Q51213973"
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The following pages link to Murine systemic thrombophilia and hemolytic uremic syndrome from a factor H point mutation. (Q51213973):
Displaying 11 items.
- In vitro evidence of complement activation in patients with sickle cell disease. (Q47163783) (← links)
- Immunological features and functional analysis of anti-CFH autoantibodies in patients with atypical hemolytic uremic syndrome (Q57472157) (← links)
- Hyperfunctional complement C3 promotes C5-dependent atypical hemolytic uremic syndrome in mice (Q61651844) (← links)
- Complement in Thrombotic Microangiopathies: Unraveling Ariadne's Thread Into the Labyrinth of Complement Therapeutics (Q64094847) (← links)
- Targeting properdin in the treatment of atypical haemolytic uraemic syndrome: better than eculizumab? (Q64993828) (← links)
- Blocking Properdin Prevents Complement-Mediated Hemolytic Uremic Syndrome and Systemic Thrombophilia (Q88954752) (← links)
- Prevention of Fatal C3 Glomerulopathy by Recombinant Complement Receptor of the Ig Superfamily (Q89080771) (← links)
- Thrombotic microangiopathies: Complement factor H: beyond aHUS (Q89938127) (← links)
- Endothelium structure and function in kidney health and disease (Q90871287) (← links)
- The Human Platelet as an Innate Immune Cell: Interactions Between Activated Platelets and the Complement System (Q92239487) (← links)
- Deficiency of Mouse FHR-1 Homolog, FHR-E, Accelerates Sepsis, and Acute Kidney Injury Through Enhancing the LPS-Induced Alternative Complement Pathway (Q97420785) (← links)