Pages that link to "Q33337391"

The following pages link to Complement factor H and hemolytic uremic syndrome (Q33337391):

Displaying 15 items.

• A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration (Q24523983) (← links)
• Hemolytic uremic syndrome: how do factor H mutants mediate endothelial damage? (Q33337903) (← links)
• Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome (Q33347509) (← links)
• Attempted treatment of factor H deficiency by liver transplantation (Q33359768) (← links)
• HUS and atypical HUS. (Q33441069) (← links)
• Defective complement inhibitory function predisposes to renal disease (Q34465747) (← links)
• Structure of vaccinia complement protein in complex with heparin and potential implications for complement regulation (Q34829635) (← links)
• Anti-mouse properdin TSR 5/6 monoclonal antibodies block complement alternative pathway-dependent pathogenesis (Q35149952) (← links)
• Access to the complement factor B scissile bond is facilitated by association of factor B with C3b protein (Q35372492) (← links)
• Clinical aspects and molecular basis of primary deficiencies of complement component C3 and its regulatory proteins factor I and factor H. (Q36405585) (← links)
• Anti-complement activity of the Ixodes scapularis salivary protein Salp20. (Q36422019) (← links)
• Complement factor H in AMD: Bridging genetic associations and pathobiology. (Q46022690) (← links)
• The role of properdin in the assembly of the alternative pathway C3 convertases of complement (Q46814862) (← links)
• Determination of complement factor H functional polymorphisms (V62I, Y402H, and E936D) using sequence-specific primer PCR and restriction fragment length polymorphisms. (Q54577923) (← links)
• [The complement system and its possible role in the pathogenesis of age-related macular degeneration (AMD)] (Q81332748) (← links)