Pages that link to "Q33333985"
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The following pages link to Factor H and the pathogenesis of renal diseases (Q33333985):
Displaying 30 items.
- Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II) (Q24317382) (← links)
- Pathogenesis of thrombotic microangiopathies (Q24658043) (← links)
- Current treatment of atypical hemolytic uremic syndrome (Q27003211) (← links)
- Alternative Complement Pathway Deregulation Is Correlated with Dengue Severity (Q27489374) (← links)
- MPGN II--genetically determined by defective complement regulation? (Q28267245) (← links)
- Pig complement regulator factor H: molecular cloning and functional characterization. (Q33193498) (← links)
- Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome. (Q33335833) (← links)
- Complement factor H and the haemolytic uraemic syndrome (Q33339462) (← links)
- Clostridium difficile colitis associated with hemolytic-uremic syndrome. (Q33348240) (← links)
- Familial mesangio-capillary glomerulonephritis with initial presentation as haemolytic uraemic syndrome (Q33358128) (← links)
- Factor H binds to washed human platelets. (Q33364421) (← links)
- An interactive web database of factor H-associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease-associated mutations (Q33369200) (← links)
- A case of atypical hemolytic uremic syndrome with a transient decrease in complement factor H. (Q33369638) (← links)
- Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome. (Q33370511) (← links)
- Assesment, treatment and prevention of atypical hemolytic uremic syndrome (Q33405916) (← links)
- Complement control protein factor H: the good, the bad, and the inadequate. (Q34067107) (← links)
- Research on complement: old issues revisited and a novel sphere of influence. (Q35155940) (← links)
- Complement and the Kidney (Q35538695) (← links)
- Chlamydia infection status, genotype, and age-related macular degeneration. (Q35673398) (← links)
- The molecular basis for hereditary porcine membranoproliferative glomerulonephritis type II: point mutations in the factor H coding sequence block protein secretion (Q35748229) (← links)
- Crucial genes and pathways in chicken germ stem cell differentiation (Q35861049) (← links)
- Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases (Q35959606) (← links)
- Susceptibility to advanced age-related macular degeneration and alleles of complement factor H, complement factor B, complement component 2, complement component 3, and age-related maculopathy susceptibility 2 genes in a Mexican population. (Q36350405) (← links)
- Renal disease associated with inherited disorders of the complement system (Q37310948) (← links)
- Mechanism of inflammation in age-related macular degeneration: an up-to-date on genetic landmarks. (Q38173896) (← links)
- A rare case: childhood-onset C3 glomerulonephritis due to homozygous factor H deficiency (Q38783519) (← links)
- Genetic and environmental factors influencing the human factor H plasma levels (Q43958315) (← links)
- Complement in glomerulonephritis (Q74391159) (← links)
- Inherited factor H dysfunction and complement-associated glomerulonephritis in renal grafts of first and second transplantations (Q77490373) (← links)
- Membranoproliferative pattern of glomerular injury associated with complement component 9 deficiency due to Arg95Stop mutation (Q82352138) (← links)