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

Evaluation of the significance of complement-related genes mutations in atypical postinfectious glomerulonephritis: a pilot study.

International urology and nephrology - 1 Apr 2024

Xu Feng, Zhang Changming, Zhang Mingchao, Zhu Xiaodong, Cheng Shuiqin, Cheng Zhen, Zeng Caihong, Jiang Song

Abstract excerpt

BACKGROUND: Postinfectious glomerulonephritis with C3-dominant glomerular deposition (C3-PIGN) involves C3-dominant glomerular deposition without immunoglobulin. Atypical C3-PIGN involves persistent hypocomplementemia. We investigated the clinical features and explored complement-related gene mutations in atypical PIGN patients. METHODS: We enrolled atypical C3-PIGN patients and collected data regarding the...

Read the complete abstract on PubMed

Topics

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

Share to Glomerulonephritis
Share to Kidney Glomerulus

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lectins

Share to Mutation

Share to Pilot Projects

Source

Open in PubMed Open full text

Identifiers

PMID: 37845399
DOI: 10.1007/s11255-023-03831-7
PMCID: PMC10924015

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Evaluation of the significance of complement-related genes mutations in atypical postinfectious glomerulonephritis: a pilot study.PMID 37845399Read ↗

Acquired and genetic determinants of disease phenotype and therapeutic strategies in C3 glomerulopathy and immunoglobulin-associated MPGNSemantic proximity Read ↗

Genetic analysis of CFH and MCP in Egyptian patients with immune-complex proliferative glomerulonephritisSemantic proximity Read ↗

C3 glomerulonephritis: clinicopathological findings, complement abnormalities, glomerular proteomic profile, treatment, and follow-up.Semantic proximity Read ↗

Genetic analysis of the complement pathway in C3 glomerulopathy.Semantic proximity Read ↗

C3 Glomerulopathy: A Current Perspective in an Evolving LandscapeSemantic proximity Read ↗

Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 Glomerulopathy.Semantic proximity Read ↗

From post-infectious glomerulonephritis to complement-mediated aHUS: a diagnostic challenge.Semantic proximity Read ↗

Rare Variants in Complement Gene in C3 Glomerulopathy and Immunoglobulin-Mediated Membranoproliferative GNSemantic proximity Read ↗

Defining Nephritic Factors as Diverse Drivers of Systemic Complement Dysregulation in C3 GlomerulopathySemantic proximity Read ↗

Different types of glomerulonephritis associated with the dysregulation of the complement alternative pathway in 2 brothers: A case report.Semantic proximity Read ↗

Genetic and acquired abnormalities in C3 glomerulopathy and primary immune complex-mediated MPGNSemantic proximity Read ↗

Long-term data on two sisters with C3GN due to an identical, homozygous CFH mutation and autoantibodies.Semantic proximity Read ↗

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