Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals. (Q33378236)

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English	Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals.	scientific article

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scholarly article

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31 December 2019

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Translational mini-review series on complement factor H: renal diseases associated with complement factor H: novel insights from humans and animals (English)

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31 December 2019

Matthew C Pickering

1

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31 December 2019

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H T Cook

2

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1 February 2008

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31 December 2019

Clinical and Experimental Immunology

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31 December 2019

151

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31 December 2019

2

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31 December 2019

210-230

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Europe PubMed Central

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31 December 2019

Familial hemolytic-uremic syndrome and homozygous factor H deficiency

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2249.2007.03574.X

21 January 2018

Porcine membranoproliferative glomerulonephritis type II: an autosomal recessive deficiency of factor H.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2249.2007.03574.X

21 January 2018

The molecular basis for hereditary porcine membranoproliferative glomerulonephritis type II: point mutations in the factor H coding sequence block protein secretion

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2249.2007.03574.X

21 January 2018

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/10.1111%2FJ.1365-2249.2007.03574.X

21 January 2018

Factor I is required for the development of membranoproliferative glomerulonephritis in factor H-deficient mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Translational mini-review series on complement factor H: genetics and disease associations of human complement factor H.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

New approaches to the treatment of dense deposit disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Anti factor H autoantibodies block C-terminal recognition function of factor H in hemolytic uremic syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Dense deposit disease is not a membranoproliferative glomerulonephritis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Complete factor H deficiency-associated atypical hemolytic uremic syndrome in a neonate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Prevention of C5 activation ameliorates spontaneous and experimental glomerulonephritis in factor H-deficient mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Complement factor I deficiency associated with recurrent infections, vasculitis and immune complex glomerulonephritis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Comparison of surface recognition and C3b binding properties of mouse and human complement factor H

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Recurrence of membranoproliferative glomerulonephritis type II in renal allografts: The North American Pediatric Renal Transplant Cooperative Study experience

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Complement factor H polymorphism in age-related macular degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Complement factor H polymorphism and age-related macular degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

The human complement factor H: functional roles, genetic variations and disease associations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Familial haemolytic uraemic syndrome and an MCP mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

ISOLATION OF BETA IF-GLOBULIN FROM HUMAN SERUM AND ITS CHARACTERIZATION AS THE FIFTH COMPONENT OF COMPLEMENT.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Host recognition and target differentiation by factor H, a regulator of the alternative pathway of complement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Deficiency of human complement factor I associated with lowered factor H.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Molecular basis for factor H and FHL-1 deficiency in an Italian family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Nephritogenic lambda light chain dimer: a unique human miniautoantibody against complement factor H

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Human complement factor H deficiency associated with hemolytic uremic syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor H.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Genetic studies into inherited and sporadic hemolytic uremic syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Mapping of the domains required for decay acceleration activity of the human factor H-like protein 1 and factor H.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Heterozygous and homozygous factor H deficiency states in a Dutch family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Complement C3 gene expression and regulation in human glomerular epithelial cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Extensive complement activation in hereditary porcine membranoproliferative glomerulonephritis type II (porcine dense deposit disease)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Hereditary complement factor I deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Inherited factor H deficiency and collagen type III glomerulopathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Idiopathic mesangiocapillary glomerulonephritis. Comparison of types I and II in children and adults and long-term prognosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Recurrence of an original glomerular lesion in three renal allografts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Serum C'3 lytic system in patients with glomerulonephritis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Hypocomplementemic glomerulonephritis in an infant and mother. Evidence for an abnormal form of C3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Human complement factor H. Tissue specificity in the expression of three different mRNA species

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Dense deposit disease: a variant of membranoproliferative glomerulonephritis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Control of the amplification convertase of complement by the plasma protein beta1H

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Membranoproliferative glomerulonephritis with disruption of the glomerular basement membrane

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Mesangiocapillary glomerulonephritis with dense "deposits" in the basement membranes of the kidney

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Prolonged complement activation in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Recurrence of dense deposits in transplanted kidney: II. Serum complement and nephritic factor profiles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Recurrence of dense deposits in transplanted kidneys: I. Sequential survey of the lesions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Immunofluorescence studies of dense deposit disease. The presence of railroad tracks and mesangial rings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Regulation by membrane sialic acid of β1H-dependent decay-dissociation of amplification C3 convertase of the alternative complement pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

Reaction mechanisms of beta1H globulin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2276951

31 October 2018

C3 and C4 gene expression and interferon-gamma-mediated regulation in human glomerular mesangial cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of C3 and factor H synthesis of human glomerular mesangial cells by IL-1 and interferon-gamma

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Secondary membranoproliferative glomerulonephritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glomerulonephritis in a patient with complement factor I deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Renal transplantation in patients with dense deposit disease: morphological characteristics of recurrent disease and clinical outcome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypocomplementaemia due to a genetic deficiency of beta 1H globulin

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biological significance of the C3 nephritic factor in membranoproliferative glomerulonephritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An inherited defect in the C3 convertase, C3b,Bb, associated with glomerulonephritis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C3 nephritic factor and hypocomplementaemia in a clinically healthy individual

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dense intramembranous deposit disease: new pathologic features

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

H deficiency in two brothers with atypical dense intramembranous deposit disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ultrastructural localization of the membrane attack complex of complement in human renal tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Combined homozygous factor H and heterozygous C2 deficiency in an Italian family

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary, complete deficiency of complement factor H associated with recurrent meningococcal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of complement regulatory domains in human factor H

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Eradication of porcine factor H deficiency in Norway

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In situ complement activation in porcine membranoproliferative glomerulonephritis type II

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dense Deposits Disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human alternative complement pathway: membrane-associated sialic acid regulates the competition between B and beta1 H for cell-bound C3b

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activation of the alternative complement pathway: recognition of surface structures on activators by bound C3b

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The physiological breakdown of the third component of human complement

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Composition of nephritic factor-generated glomerular deposits in membranoproliferative glomerulonephritis type 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor H deficiency and fibrillary glomerulopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of nephritogenicity of systemic activation of the alternate complement pathway

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C3 nephritic factor (C3NeF): stabilization of fluid phase and cell-bound alternative pathway convertase

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Complement Abnormalities of Lipodystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18190458

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1111/J.1365-2249.2007.03574.X

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18190458%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

0 references

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18190458%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

ResearchGate publication ID

0 references

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