Streptococcus pneumoniae From Patients With Hemolytic Uremic Syndrome Binds Human Plasminogen via the Surface Protein PspC and Uses Plasmin to Damage Human Endothelial Cells.

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Modeling Hemolytic-Uremic Syndrome: In-Depth Characterization of Distinct Murine Models Reflecting Different Features of Human Disease.Aspf2 From Recruits Human Immune Regulators for Immune Evasion and Cell Damage

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Streptococcus pneumoniae From Patients With Hemolytic Uremic Syndrome Binds Human Plasminogen via the Surface Protein PspC and Uses Plasmin to Damage Human Endothelial Cells.

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2017 nî lūn-bûn

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2017年学术文章

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Streptococcus pneumoniae From ...... amage Human Endothelial Cells.

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Streptococcus pneumoniae From ...... amage Human Endothelial Cells.

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Streptococcus pneumoniae From ...... amage Human Endothelial Cells.

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Streptococcus pneumoniae From ...... amage Human Endothelial Cells.

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Streptococcus pneumoniae From ...... amage Human Endothelial Cells.

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Christian Meinel

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Christine Skerka

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Franziska Hörhold

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Giuseppina Spartà

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Hans-Martin Dahse

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Marc Thilo Figge

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Martin Westermann

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Rainer König

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Sina M Coldewey

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Sven Hammerschmidt

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P2860

Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome

Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome

The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models

Human complement control and complement evasion by pathogenic microbes--tipping the balance

Mutations in factor H reduce binding affinity to C3b and heparin and surface attachment to endothelial cells in hemolytic uremic syndrome.

Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome.

Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome.

Anti factor H autoantibodies block C-terminal recognition function of factor H in hemolytic uremic syndrome.

Streptococcus pneumoniae-associated hemolytic uremic syndrome.

The complement fitness factor H: role in human diseases and for immune escape of pathogens, like pneumococci.

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10.1093/INFDIS/JIX305

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217

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Peter F Zipfel

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2017-08-26T00:00:00Z

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Streptococcus pneumoniae From Patients With Hemolytic Uremic Syndrome Binds Human Plasminogen via the Surface Protein PspC and Uses Plasmin to Damage Human Endothelial Cells.

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P2860

P2860

Streptococcus pneumoniae From Patients With Hemolytic Uremic Syndrome Binds Human Plasminogen via the Surface Protein PspC and Uses Plasmin to Damage Human Endothelial Cells.

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