List of works - Stefan Heinen

A lymphatic defect causes ocular hypertension and glaucoma in mice

scientific article (publication date: October 2014)

Binding of complement factor H to endothelial cells is mediated by the carboxy-terminal glycosaminoglycan binding site

scientific article published on October 2005

C3 deposition glomerulopathy due to a functional factor H defect

scientific article published on 16 July 2008

Complement and diseases: defective alternative pathway control results in kidney and eye diseases

scientific article

De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome

scientific article

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

scientific article

Different factor H-related protein patterns in siblings with typical hemolytic uremic syndrome

scientific article published on 21 April 2011

Factor H and atypical hemolytic uremic syndrome: mutations in the C-terminus cause structural changes and defective recognition functions

scientific article

Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency

scientific article

Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement deposition on platelets and their activation

scientific article

Factor H-related protein 1 (CFHR-1) inhibits complement C5 convertase activity and terminal complex formation

scientific article published on 15 June 2009

Focused ultrasound delivery of a selective TrkA agonist rescues cholinergic function in a mouse model of Alzheimer's disease

scientific article published on 22 January 2020

Hemolytic uremic syndrome: a factor H mutation (E1172Stop) causes defective complement control at the surface of endothelial cells

scientific article

Monitoring and modeling treatment of atypical hemolytic uremic syndrome

scientific article

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

scientific article

The human brain endothelial barrier: transcytosis of AAV9, transduction by AAV2: An Editorial Highlight for 'Trafficking of adeno-associated virus vectors across a model of the blood-brain barrier; a comparative study of transcytosis and transductio

scientific article published on 15 December 2016

Thrombotic microangiopathies: new insights and new challenges

scientific article

List of works by Stefan Heinen

A lymphatic defect causes ocular hypertension and glaucoma in mice

Binding of complement factor H to endothelial cells is mediated by the carboxy-terminal glycosaminoglycan binding site

C3 deposition glomerulopathy due to a functional factor H defect

Complement and diseases: defective alternative pathway control results in kidney and eye diseases

De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome

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

Different factor H-related protein patterns in siblings with typical hemolytic uremic syndrome

Factor H and atypical hemolytic uremic syndrome: mutations in the C-terminus cause structural changes and defective recognition functions

Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency

Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement deposition on platelets and their activation

Factor H-related protein 1 (CFHR-1) inhibits complement C5 convertase activity and terminal complex formation

Focused ultrasound delivery of a selective TrkA agonist rescues cholinergic function in a mouse model of Alzheimer's disease

Hemolytic uremic syndrome: a factor H mutation (E1172Stop) causes defective complement control at the surface of endothelial cells

Monitoring and modeling treatment of atypical hemolytic uremic syndrome

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

The human brain endothelial barrier: transcytosis of AAV9, transduction by AAV2: An Editorial Highlight for 'Trafficking of adeno-associated virus vectors across a model of the blood-brain barrier; a comparative study of transcytosis and transductio

Thrombotic microangiopathies: new insights and new challenges