Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Clustering of Missense Mutations in the C-Terminal Region of Factor H in Atypical Hemolytic Uremic Syndrome

1 Feb 2001

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Complement system in diseases
Share to Erythrocyte Function and Pathophysiology
Share to Iron Metabolism and Disorders

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 11170895
DOI: 10.1086/318201

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clustering of Missense Mutations in the C-Terminal Region of Factor H in Atypical Hemolytic Uremic SyndromePMID 11170895Read ↗

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

Functional characterization of two novel non-synonymous alterations in CD46 and a Q950H change in factor H found in atypical hemolytic uremic syndrome patientsSemantic proximity Read ↗

Factor H genotype-phenotype correlations: lessons from aHUS, MPGN II, and AMD.Semantic proximity Read ↗

Clinical characterization and identification of rare genetic variants in atypical hemolytic uremic syndrome: A Swedish retrospective observational study.Semantic proximity Read ↗

Structural and functional characterization of factor H mutations associated with atypical hemolytic uremic syndrome.Semantic proximity Read ↗

The genetics of atypical hemolytic uremic syndromeSemantic proximity Read ↗

The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models.Semantic proximity Read ↗

A Novel Non-Synonymous Polymorphism (p.Arg240His) in C4b-Binding Protein Is Associated with Atypical Hemolytic Uremic Syndrome and Leads to Impaired Alternative Pathway Cofactor ActivitySemantic proximity Read ↗

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

Genetics and complement in atypical HUS.Semantic proximity Read ↗

Genetic analysis and functional characterization of novel mutations in a series of patients with atypical hemolytic uremic syndrome.Semantic proximity Read ↗

Analysis of patients with atypical hemolytic uremic syndrome treated at the Mie University Hospital: concentration of C3 p.I1157T mutation.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.