Atypical haemolytic uraemic syndrome and mutations in complement regulator genes (Q33368691)

26 July 2017

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title

Atypical haemolytic uraemic syndrome and mutations in complement regulator genes (English)

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Véronique Frémeaux-Bacchi

26 July 2017

author

series ordinal

2

object named as

Véronique Frémeaux-Bacchi

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26 July 2017

Marie-Agnès Dragon-Durey

series ordinal

1

object named as

Marie-Agnès Dragon-Durey

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publication date

11 November 2005

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Seminars in Immunopathology

26 July 2017

published in

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26 July 2017

volume

27

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26 July 2017

issue

3

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26 July 2017

page(s)

359-374

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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

26 July 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00281-005-0003-2

Familial hemolytic-uremic syndrome and homozygous factor H deficiency

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00281-005-0003-2

Disruption of disulfide bonds is responsible for impaired secretion in human complement factor H deficiency

21 January 2018

1 reference

12 December 2020

Shiga-toxin-producing Escherichia coli and haemolytic uraemic syndrome

1 reference

12 December 2020

Enteropathogens associated with childhood diarrhea in Italy. The Italian Study Group on Gastrointestinal Infections

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12 December 2020

Familial hemolytic-uremic syndrome in three generations

1 reference

12 December 2020

Dissecting Sites Important for Complement Regulatory Activity in Membrane Cofactor Protein (MCP; CD46)

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12 December 2020

Participation of protein kinases in complement C5b-9-induced shedding of platelet plasma membrane vesicles

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12 December 2020

Complement factor I deficiency in a family with recurrent infections

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12 December 2020

Genetic studies into inherited and sporadic hemolytic uremic syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

A complement receptor locus: genes encoding C3b/C4b receptor and C3d/Epstein-Barr virus receptor map to 1q32

1 reference

12 December 2020

Human complement factor H deficiency associated with hemolytic uremic syndrome.

1 reference

12 December 2020

Severe ADAMTS13 deficiency in adult idiopathic thrombotic microangiopathies defines a subset of patients characterized by various autoimmune manifestations, lower platelet count, and mild renal involvement

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial haemolytic uraemic syndrome and an MCP mutation

1 reference

12 December 2020

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

1 reference

12 December 2020

Anaphylatoxins and infectious and non-infectious inflammatory diseases

1 reference

12 December 2020

Hereditary complement factor I deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome

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12 December 2020

Combined kidney and liver transplantation for familial haemolytic uraemic syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

The development of atypical haemolytic-uraemic syndrome is influenced by susceptibility factors in factor H and membrane cofactor protein: evidence from two independent cohorts

1 reference

12 December 2020

Analysis of C5a receptor by monoclonal antibody

1 reference

12 December 2020

Renal microvascular injury induced by antibody to glomerular endothelial cells is mediated by C5b-9

1 reference

12 December 2020

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

1 reference

12 December 2020

Genomic organization and polymorphisms of the human C3d/Epstein-Barr virus receptor

1 reference

12 December 2020

Human genes for three complement components that regulate the activation of C3 are tightly linked

1 reference

12 December 2020

Disulfide bonds are localized within the short consensus repeat units of complement regulatory proteins: C4b-binding protein

1 reference

12 December 2020

Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome

1 reference

12 December 2020

Challenges in the management of infantile factor H associated hemolytic uremic syndrome.

1 reference

12 December 2020

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

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12 December 2020

Recurrent haemolytic-uraemic syndrome with hypocomplementaemia: a case report

1 reference

12 December 2020

Predisposition to atypical hemolytic uremic syndrome involves the concurrence of different susceptibility alleles in the regulators of complement activation gene cluster in 1q32.

1 reference

12 December 2020

Human complement C3b inactivator: isolation, characterization, and demonstration of an absolute requirement for the serum protein beta1H for cleavage of C3b and C4b in solution

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12 December 2020

A new model of renal microvascular endothelial injury

1 reference

12 December 2020

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12 December 2020

C5b-9 membrane attack complex mediates endothelial cell apoptosis in experimental glomerulonephritis

1 reference

12 December 2020

Hypocomplementaemia due to a genetic deficiency of beta 1H globulin

1 reference

12 December 2020

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

1 reference

12 December 2020

Complement c3a and c5a induce different signal transduction cascades in endothelial cells

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

CD46: expanding beyond complement regulation

1 reference

12 December 2020

10.1007/S00281-005-0003-2

Identifiers

DOI

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Dimensions Publication ID

26 July 2017

1034722638

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