(Q33337903)

25 July 2017

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title

Hemolytic uremic syndrome: how do factor H mutants mediate endothelial damage? (English)

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25 July 2017

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Zipfel PF

1

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25 July 2017

publication date

1 July 2001

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25 July 2017

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25 July 2017

volume

22

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25 July 2017

issue

7

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25 July 2017

page(s)

345-348

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

25 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4906%2801%2901972-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4906%2801%2901972-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4906%2801%2901972-X

7 January 2021

Factor H and disease: a complement regulator affects vital body functions.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4906%2801%2901972-X

7 January 2021

The C-terminus of factor H: monoclonal antibodies inhibit heparin binding and identify epitopes common to factor H and factor H-related proteins

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4906%2801%2901972-X

7 January 2021

Human complement regulators: a major target for pathogenic microorganisms

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4906%2801%2901972-X

7 January 2021

Human factor H deficiency. Mutations in framework cysteine residues and block in H protein secretion and intracellular catabolism

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4906%2801%2901972-X

7 January 2021

Hereditary porcine membranoproliferative glomerulonephritis type II is caused by factor H deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4906%2801%2901972-X

7 January 2021

Complement factor H and hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4906%2801%2901972-X

7 January 2021

Hemolytic Uremic Syndrome in Families

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4906%2801%2901972-X

7 January 2021

Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4906%2801%2901972-X

7 January 2021

Interferon gamma induces synthesis of complement alternative pathway proteins by human endothelial cells in culture

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4906%2801%2901972-X

7 January 2021

Regulation of the activity of platelet-bound C3 convertase of the alternative pathway of complement by platelet factor H

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4906%2801%2901972-X

7 January 2021

10.1016/S1471-4906(01)01972-X

Identifiers

DOI

1 reference

25 July 2017

1 reference