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Inherited complement regulatory protein deficiency predisposes to human disease in acute injury and chronic inflammatory statesthe examples of vascular damage in atypical hemolytic uremic syndrome and debris accumulation in age-related macular degen

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Europe PubMed Central

PubMed publication ID

26 July 2017

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Europe PubMed Central

Inherited complement regulatory protein deficiency predisposes to human disease in acute injury and chronic inflammatory statesthe examples of vascular damage in atypical hemolytic uremic syndrome and debris accumulation in age-related macular degen (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

atypical hemolytic uremic syndrome

1 reference

based on heuristic

inferred from title

protein deficiency

1 reference

based on heuristic

inferred from title

object named as

David Kavanagh

2

0 references

author name string

Anna Richards

1

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

John P Atkinson

3

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

publication date

1 January 2007

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Advances in Immunology

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Europe PubMed Central

PubMed publication ID

26 July 2017

96

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Europe PubMed Central

PubMed publication ID

26 July 2017

141-177

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

The simple design of complement factor H: Looks can be deceiving

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Inherited complete factor I deficiency associated with systemic lupus erythematosus, higher susceptibility to infection and low levels of factor H

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Complement activation and complement receptors in systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Rheumatic syndromes associated with complement deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Role of membrane cofactor protein (CD46) in regulation of C4b and C3b deposited on cells

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Secondary structure of a complement control protein module by two-dimensional 1H NMR

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Outcome of renal transplantation in patients with non-Shiga toxin-associated hemolytic uremic syndrome: prognostic significance of genetic background

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Cooperation between decay-accelerating factor and membrane cofactor protein in protecting cells from autologous complement attack

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Innate autoimmunity

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Four viruses, two bacteria, and one receptor: membrane cofactor protein (CD46) as pathogens' magnet

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Attempted treatment of factor H deficiency by liver transplantation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

His-384 Allotypic Variant of Factor H Associated with Age-related Macular Degeneration Has Different Heparin Binding Properties from the Non-disease-associated Form

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of complement alternative pathway proteins by endothelial cells. Differential regulation by interleukin 1 and glucocorticoids

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Ontogeny of complement regulatory proteins - concentrations of factor h, factor I, c4b-binding protein, properdin and vitronectin in healthy children of different ages and in adults

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Recurrence of hemolytic uremic syndrome after live related renal transplantation associated with subsequent de novo disease in the donor

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Complement factor H polymorphism and age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Insights into hemolytic uremic syndrome: segregation of three independent predisposition factors in a large, multiple affected pedigree

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Associative and structural properties of the region of complement factor H encompassing the Tyr402His disease-related polymorphism and its interactions with heparin

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Complement deficiency states and meningococcal disease

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Age-related macular degeneration--emerging pathogenetic and therapeutic concepts

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

C-Reactive protein binds to apoptotic cells, protects the cells from assembly of the terminal complement components, and sustains an antiinflammatory innate immune response: implications for systemic autoimmunity

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

CD46 in Neisseria pathogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Variation in factor B (BF) and complement component 2 (C2) genes is associated with age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

An integrated hypothesis that considers drusen as biomarkers of immune-mediated processes at the RPE-Bruch's membrane interface in aging and age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Extended haplotypes in the complement factor H (CFH) and CFH-related (CFHR) family of genes protect against age-related macular degeneration: characterization, ethnic distribution and evolutionary implications

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Complement factor H variant increases the risk of age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Functional properties of complement factor H-related proteins FHR-3 and FHR-4: binding to the C3d region of C3b and differential regulation by heparin

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Disease-associated sequence variations congregate in a polyanion recognition patch on human factor H revealed in three-dimensional structure

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Structure shows that a glycosaminoglycan and protein recognition site in factor H is perturbed by age-related macular degeneration-linked single nucleotide polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Effect of eculizumab on hemolysis and transfusion requirements in patients with paroxysmal nocturnal hemoglobinuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The complement inhibitor eculizumab in paroxysmal nocturnal hemoglobinuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The role of properdin in the assembly of the alternative pathway C3 convertases of complement

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The regulators of complement activation (RCA) gene cluster

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Susceptibility genes for age-related maculopathy on chromosome 10q26

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The C-terminus of complement factor H is essential for host cell protection

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Atypical haemolytic uraemic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The decay accelerating factor mutation I197V found in hemolytic uraemic syndrome does not impair complement regulation.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Screening for complement system abnormalities in patients with atypical hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Complement regulatory genes and hemolytic uremic syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

T-cell regulation: with complements from innate immunity

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Activation of human CD4+ cells with CD3 and CD46 induces a T-regulatory cell 1 phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Opsonization of apoptotic cells and its effect on macrophage and T cell immune responses

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Complement factor H polymorphism in age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A Corresponding Tyrosine Residue in the C2/Factor B Type A Domain Is a Hot Spot in the Decay Acceleration of the Complement C3 Convertases

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Y402H polymorphism of complement factor H affects binding affinity to C-reactive protein

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Association of the Y402H polymorphism in complement factor H gene and neovascular age-related macular degeneration in Chinese patients

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Control of the complement system.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Emerging roles and new functions of CD46

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Modeling how CD46 deficiency predisposes to atypical hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Allelic differences in hemolytic activity and protein concentration of BF molecules are found in association with particular HLA haplotypes

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The role of complement in the development of systemic lupus erythematosus

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of pigment epithelium derived factor and vascular endothelial growth factor in choroidal neovascular membranes and polypoidal choroidal vasculopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Inhibition of complement activation on the surface of cells after incorporation of decay-accelerating factor (DAF) into their membranes

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Complement-dependent clearance of apoptotic cells by human macrophages

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The murine complement regulator Crry: new insights into the immunobiology of complement regulation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Apoptosis and autoimmunity

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Hemolytic Uremic Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial haemolytic uraemic syndrome and an MCP mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Membrane cofactor protein (CD46) protects cells from complement-mediated attack by an intrinsic mechanism

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The alternative pathway of complement

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Systemic lupus erythematosus, complement deficiency, and apoptosis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Spontaneous hemolytic uremic syndrome triggered by complement factor H lacking surface recognition domains

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical aspects and molecular basis of primary deficiencies of complement component C3 and its regulatory proteins factor I and factor H.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Combined kidney and liver transplantation for familial haemolytic uraemic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Hemolytic uremic syndrome: a fatal outcome after kidney and liver transplantation performed to correct factor h gene mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

CD46: expanding beyond complement regulation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Targeted and restricted complement activation on acrosome-reacted spermatozoa

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Glomerulonephritis in a patient with complement factor I deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Favorable long-term outcome after liver-kidney transplant for recurrent hemolytic uremic syndrome associated with a factor H mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Functional analysis in serum from atypical Hemolytic Uremic Syndrome patients reveals impaired protection of host cells associated with mutations in factor H.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The factor H variant associated with age-related macular degeneration (His-384) and the non-disease-associated form bind differentially to C-reactive protein, fibromodulin, DNA, and necrotic cells

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Properdin can initiate complement activation by binding specific target surfaces and providing a platform for de novo convertase assembly

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Deficient alternative complement pathway activation due to factor D deficiency by 2 novel mutations in the complement factor D gene in a family with meningococcal infections

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Role for the alternative complement pathway in ischemia/reperfusion injury

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The central role of the alternative complement pathway in human disease

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

No association of complement factor H gene polymorphism and age-related macular degeneration in the Japanese population.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Epidemiology of age-related maculopathy: a review

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Atypical haemolytic uraemic syndrome associated with a hybrid complement gene

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

The molecular basis of hereditary complement factor I deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Complement. Second of two parts

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Complement. First of two parts

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Erythrocyte complement receptor type 1, immune complexes, and the rheumatic diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Biosynthesis of the complement components and the regulatory proteins of the alternative complement pathway by human peripheral blood monocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A critical role for murine complement regulator crry in fetomaternal tolerance

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Restoration by purified C3b inactivator of complement-mediated function in vivo in a patient with C3b inactivator deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Origin of the fourth component of complement related Chido and Rodgers blood group antigens

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2776%2807%2996004-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0065-2776(07)96004-6

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

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