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Your search keyword '"Marchbank, Kevin J."' showing total 242 results

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242 results on '"Marchbank, Kevin J."'

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1. Description and Cross-Sectional Analyses of 25,880 Adults and Children in the UK National Registry of Rare Kidney Diseases Cohort

2. Comprehensive functional characterization of complement factor I rare variant genotypes identified in the SCOPE geographic atrophy cohort

3. Effects of rare kidney diseases on kidney failure: a longitudinal analysis of the UK National Registry of Rare Kidney Diseases (RaDaR) cohort

4. Atypical hemolytic uremic syndrome in the era of terminal complement inhibition: an observational cohort study

5. A solid approach to biopharmaceutical stabilisation

7. Description and cross-sectional analyses of 25,880 adults and children in the UK National Registry of Rare Kidney Diseases cohort

8. Long-term outcomes and response to treatment in diacylglycerol kinase epsilon nephropathy

9. Effects of rare kidney diseases on kidney failure: a longitudinal analysis of the UK National Registry of Rare Kidney Diseases (RaDaR) cohort

10. Atypical hemolytic uremic syndrome in the era of terminal complement inhibition: an observational cohort study

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

14. Factor H autoantibody is associated with atypical hemolytic uremic syndrome in children in the United Kingdom and Ireland

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

18. A novel method for real-time analysis of the complement C3b:FH:FI complex reveals dominant negative CFI variants in age-related macular degeneration

22. Factor H autoantibodies in membranoproliferative glomerulonephritis

25. Contribution of animal models to the mechanistic understanding of Alternative Pathway and Amplification Loop (AP/AL)‐driven Complement‐mediated Diseases.

27. Whole-genome sequencing of patients with rare diseases in a national health system

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

29. C3 Glomerulopathy and Related Disorders in Children

32. Insights Into the Structure-Function Relationships of Dimeric C3d Fragments

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

34. Publisher Correction:Whole-genome sequencing of a sporadic primary immunodeficiency cohort (Nature, (2020), 583, 7814, (90-95), 10.1038/s41586-020-2265-1)

35. Whole-genome sequencing of a sporadic primary immunodeficiency cohort

38. Bayesian Inference Associates Rare KDR Variants With Specific Phenotypes in Pulmonary Arterial Hypertension

40. Successful simultaneous liver-kidney transplantation for renal failure associated with hereditary complement C3 deficiency

44. Utilization of Staphylococcal Immune Evasion Protein Sbi as a Novel Vaccine Adjuvant

45. Large expert-curated database for benchmarking document similarity detection in biomedical literature search

46. Large expert-curated database for benchmarking document similarity detection in biomedical literature search

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