Structure of complement factor H carboxyl-terminus reveals molecular basis of atypical haemolytic uremic syndrome (Q24543850)

6 July 2017

title

Structure of complement factor H carboxyl-terminus reveals molecular basis of atypical haemolytic uremic syndrome (English)

1 reference

6 July 2017

T Sakari Jokiranta

1

1 reference

6 July 2017

Veli-Pekka Jaakola

2

1 reference

6 July 2017

Markus J Lehtinen

3

1 reference

6 July 2017

Maria Pärepalo

4

1 reference

6 July 2017

Seppo Meri

5

1 reference

6 July 2017

Adrian Goldman

6

1 reference

6 July 2017

language of work or name

English

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publication date

6 April 2006

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6 July 2017

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6 July 2017

volume

25

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6 July 2017

issue

8

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6 July 2017

page(s)

1784-1794

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Interaction of beta1H globulin with cell-bound C3b: quantitative analysis of binding and influence of alternative pathway components on binding

6 July 2017

cites work

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24 March 2017

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24 March 2017

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24 March 2017

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24 March 2017

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

7 April 2017

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

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Structure of vaccinia complement protein in complex with heparin and potential implications for complement regulation

27 September 2017

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Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases

27 September 2017

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Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease

27 September 2017

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Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome

27 September 2017

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Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries

27 September 2017

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

27 September 2017

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Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndrome

27 September 2017

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Cutting edge: localization of the host recognition functions of complement factor H at the carboxyl-terminal: implications for hemolytic uremic syndrome

27 September 2017

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Combined kidney and liver transplantation for familial haemolytic uraemic syndrome

27 September 2017

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Molecular modelling of the C-terminal domains of factor H of human complement: a correlation between haemolytic uraemic syndrome and a predicted heparin binding site

27 September 2017

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Factor H mutations in hemolytic uremic syndrome cluster in exons 18-20, a domain important for host cell recognition

27 September 2017

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Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome.

27 September 2017

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The molecular basis of familial hemolytic uremic syndrome: mutation analysis of factor H gene reveals a hot spot in short consensus repeat 20.

27 September 2017

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27 September 2017

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Identification of three physically and functionally distinct binding sites for C3b in human complement factor H by deletion mutagenesis

27 September 2017

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Analysis of the mechanism of recognition in the complement alternative pathway using C3b-bound low molecular weight polysaccharides

27 September 2017

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Discrimination between activators and nonactivators of the alternative pathway of complement: regulation via a sialic acid/polyanion binding site on factor H

27 September 2017

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Activation of the alternative pathway of complement by monoclonal lambda light chains in membranoproliferative glomerulonephritis

27 September 2017

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Complement C3 convertase: Cell surface restriction of β1H control and generation of restriction on neuraminidase-treated cells

27 September 2017

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Lysine-dependent multipoint binding of the Borrelia burgdorferi virulence factor outer surface protein E to the C terminus of factor H.

27 September 2017

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Exceptional resistance of human H2 glioblastoma cells to complement-mediated killing by expression and utilization of factor H and factor H-like protein 1.

21 January 2018

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29 November 2018

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Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor H

29 November 2018

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29 November 2018

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Each of the three binding sites on complement factor H interacts with a distinct site on C3b

29 November 2018

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12 December 2020

Complement C3b/C3d and cell surface polyanions are recognized by overlapping binding sites on the most carboxyl-terminal domain of complement factor H

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12 December 2020

Interdomain Contact Regions and Angles Between Adjacent Short Consensus Repeat Domains

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12 December 2020

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12 December 2020

Extracellular domain of type I receptor for transforming growth factor-beta: molecular modelling using protectin (CD59) as a template

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12 December 2020

Identification of the second heparin-binding domain in human complement factor H

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12 December 2020

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7 January 2021

inferred from DOI database lookup

PROCHECK: a program to check the stereochemical quality of protein structures

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7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/SJ.EMBOJ.7601052

1 reference

OpenCitations bibliographic resource ID

6 July 2017

2671967

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

6 July 2017

1 reference