33 results on '"Sánchez-Corral, Pilar"'
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2. Contribución de variantes funcionales y cuantitativas del Factor H y las proteínas FHRs (Factor H-Related proteins) del Complemento en patología renal
3. Contribution of functional and quantitative genetic variants of Complement Factor H and Factor H-Related (FHR) proteins on renal pathology
4. Complement as a diagnostic tool in immunopathology
5. Low FHR-5 levels contribute to infection-triggered haemolytic uraemic syndrome/membranoproliferative glomerulonephritis
6. Increased alternative pathway regulation by using an anti complement regulator factor H potentiating antibody
7. Quantitative Western-blot profiles of factor H and factor H-related proteins in atypical haemolytic uraemic syndrome and C3 glomerulopathy
8. Novel duplication of the FHRs dimerization domain associated with C3G
9. Heterogeneity but individual constancy of epitopes, isotypes and avidity of factor H autoantibodies in atypical hemolytic uremic syndrome
10. Complement factor H, FHR-3 and FHR-1 variants associate in an extended haplotype conferring increased risk of atypical hemolytic uremic syndrome
11. The molecular and structural bases for the association of complement C3 mutations with atypical hemolytic uremic syndrome
12. Autoantibodies to complement components in C3 glomerulopathy and atypical hemolytic uremic syndrome
13. An ELISA assay with two monoclonal antibodies allows the estimation of free factor H and identifies patients with acquired deficiency of this complement regulator
14. Complement factor H variants I890 and L1007 while commonly associated with atypical hemolytic uremic syndrome are polymorphisms with no functional significance
15. Factor H-related protein 1 neutralizes anti-factor H autoantibodies in autoimmune hemolytic uremic syndrome
16. Functional implications of the recognition of complement factor H-related protein 1 (CFHR1) by anti-factor H autoantibodies in autoimmune haemolytic uraemic syndrome
17. Proteomics-based discovery of an abnormal, internally duplicated CFHR1 protein which associates with renal pathology in a Spanish family
18. Factor H autoantibodies in a Hemolytic Uremic Syndrome patient presenting homozygous CFHR1 and CFHR4A deficiency
19. Factor H autoantibodies associated with atypical hemolytic uremic syndrome crossreact with factor H-related protein 1
20. Identification and functional characterisation of a relatively frequent CFH haplotype carrying two polymorphisms (S890I and V1007L) associated with aHUS
21. Autoimmune atypical haemolytic uraemic syndrome in the Spanish registry
22. Mutations in Proteins of the Alternative Pathway of Complement and the Pathogenesis of Atypical Hemolytic Uremic Syndrome
23. Genetic deficiency of complement factor H in a patient with age-related macular degeneration and membranoproliferative glomerulonephritis
24. Molecular characterization of complement Factor I deficiency in two Spanish families
25. Novel complement factor H mutation in SCR7 in a patient with age-related macular degeneration and membranoproliferative glomerulonephritis type II
26. Complement factor H haplotypes and copy number variations of the factor H-related genes in renal and ocular disorders
27. Description and partial characterization of the isoform pattern of complement factor H-related proteins in plasma
28. Mutations in complement factor B are associated with atypical hemolytic uremic syndrome
29. Structural and Functional Characterization of Factor H Mutations Associated with Atypical Hemolytic Uremic Syndrome
30. Clustering of Missense Mutations in the C-Terminal Region of Factor H in Atypical Hemolytic Uremic Syndrome
31. The Gene Coding for the β-Chain of C4b-Binding Protein (C4BPB) Has Become a Pseudogene in the Mouse
32. C4BPAL1, a Member of the Human Regulator of Complement Activation (RCA) Gene Cluster That Resulted from the Duplication of the Gene Coding for the α-Chain of C4b-Binding Protein
33. Proteolytic activity of the different fragments of factor B on the third component of complement (C3). Involvement of the N-terminal domain of Bb in magnesium binding
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