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Article

A mutation in factor I that is associated with atypical hemolytic uremic syndrome does not affect the function of factor I in complement regulation

8 Nov 2006

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 17084897
DOI: 10.1016/j.molimm.2006.10.005

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

A mutation in factor I that is associated with atypical hemolytic uremic syndrome does not affect the function of factor I in complement regulationPMID 17084897Read ↗

Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome.Semantic proximity Read ↗

Genetics and complement in atypical HUS.Semantic proximity Read ↗

The genetics of atypical hemolytic uremic syndromeSemantic proximity Read ↗

Atypical hemolytic uremic syndrome: the role of complement pathway gene mutation analysis.Semantic proximity Read ↗

Complement Factor H Gene Mutation Associated with Autosomal Recessive Atypical Hemolytic Uremic SyndromeSemantic proximity Read ↗

Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndrome.Semantic proximity Read ↗

Mutations in complement factor I as found in atypical hemolytic uremic syndrome lead to either altered secretion or altered function of factor I.Semantic proximity Read ↗

Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome.Semantic proximity Read ↗

Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome.Semantic proximity Read ↗

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

The C3 p.Ile1157Thr mutation associated with atypical hemolytic uremic syndrome, particularly in Japan, does not lead to disease development in several mouse models.Semantic proximity Read ↗

Factor I autoantibodies in patients with atypical hemolytic uremic syndrome: disease-associated or an epiphenomenon?Semantic proximity Read ↗

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