Reference Intervals of Factor H and Factor H-Related Proteins in Healthy Children

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Reference Intervals of Factor H and Factor H-Related Proteins in Healthy Children

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scientific article published on 02 August 2018

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wetenschappelijk artikel

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наукова стаття, опублікована у 2018

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Reference Intervals of Factor H and Factor H-Related Proteins in Healthy Children

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Reference Intervals of Factor H and Factor H-Related Proteins in Healthy Children

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Reference Intervals of Factor H and Factor H-Related Proteins in Healthy Children

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Reference Intervals of Factor H and Factor H-Related Proteins in Healthy Children

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Reference Intervals of Factor H and Factor H-Related Proteins in Healthy Children

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Reference Intervals of Factor H and Factor H-Related Proteins in Healthy Children

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P1476

Reference Intervals of Factor H and Factor H-Related Proteins in Healthy Children

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P2093

Angela Kamp

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Diana Wouters

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Ed J Nieuwenhuys

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Kyra A Gelderman

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Simone Kruithof

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Taco W Kuijpers

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Theo Rispens

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P2860

Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis

Variations in the complement regulatory genes factor H (CFH) and factor H related 5 (CFHR5) are associated with membranoproliferative glomerulonephritis type II (dense deposit disease)

The complotype: dictating risk for inflammation and infection

Comprehensive analysis of Copy Number Variation of genes at chromosome 1 and 10 loci associated with late age related macular degeneration

Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degeneration

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

Genetic analysis of the complement factor H related 5 gene in haemolytic uraemic syndrome.

Atypical hemolytic uremic syndrome and genetic aberrations in the complement factor H-related 5 gene

A novel atypical hemolytic uremic syndrome-associated hybrid CFHR1/CFH gene encoding a fusion protein that antagonizes factor H-dependent complement regulation.

Complement factor H, FHR-3 and FHR-1 variants associate in an extended haplotype conferring increased risk of atypical hemolytic uremic syndrome.

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1727

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scholarly article

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10.3389/FIMMU.2018.01727

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P407

English

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P50

Anna E van Beek

Ilse Jongerius

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2018-08-02T00:00:00Z

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P698

30116238

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6082937

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